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Keywords:

  • melanoma;
  • Akt3;
  • PTEN;
  • oncogene;
  • tumorigenesis;
  • apoptosis

Summary

  1. Top of page
  2. Summary
  3. Introduction
  4. PTEN and AKT3 in human melanomas
  5. Cellular processes regulated by PTEN/Akt3 signaling in melanomas
  6. Therapeutic potential of targeting the PTEN/Akt3 signaling cascade in melanomas
  7. Conclusions
  8. Key unanswered questions
  9. Acknowledgements
  10. References

Melanocytes undergo extensive genetic changes during transformation into aggressive melanomas. These changes deregulate genes whose aberrant activity promotes the development of this disease. The phosphoinositide-3-kinase (PI3K) and mitogen-activated protein (MAP) kinase pathways are two key signaling cascades that have been found to play prominent roles in melanoma development. These pathways relay extra-cellular signals via an ordered series of consecutive phosphorylation events from cell surface throughout the cytoplasm and nucleus regulating diverse cellular processes including proliferation, survival, invasion and angiogenesis. It is generally accepted that therapeutic agents would need to target these two pathways to be an effective therapy for the long-term treatment of advanced-stage melanoma patients. This review provides an overview of the PI3 kinase pathway focusing specifically on two members of the pathway, called PTEN and Akt3, which play important roles in melanoma development. Mechanisms leading to deregulation of these two proteins and therapeutic implications of targeting this signaling cascade to treat melanoma are detailed in this review.


Introduction

  1. Top of page
  2. Summary
  3. Introduction
  4. PTEN and AKT3 in human melanomas
  5. Cellular processes regulated by PTEN/Akt3 signaling in melanomas
  6. Therapeutic potential of targeting the PTEN/Akt3 signaling cascade in melanomas
  7. Conclusions
  8. Key unanswered questions
  9. Acknowledgements
  10. References

Identification of signaling pathways and proteins involved in melanoma progression and drug resistance has the potential to lead to the development of novel, more effective targeted therapies. Two of these pathways are the PI3K (phosphoinositide-3-kinase) and MAP (mitogen-activated protein) kinase signaling cascades involved in melanoma development by relaying extra-cellular signals to regulate diverse cellular processes including proliferation, survival, invasion, and angiogenesis (Chudnovsky et al., 2005; Hsu et al., 2002; Smalley and Herlyn, 2005). It is generally accepted in the melanoma research and clinical communities that therapeutic agents targeting these two pathways will be effective for the long-term treatment of advanced-stage patients but which members of the cascades to target remain to be established. This review provides an overview of the PI3 kinase pathway in melanoma development detailing mechanisms leading to deregulation of PTEN and Akt3 in this cascade, cellular processes regulated by these proteins and therapeutic implications of targeting these proteins to treat this deadly disease. Finally, key issues that remain to be answered concerning this important signaling cascade are discussed.

Introduction to PTEN as a cancer suppressor gene

The phosphatase and tensin homologue deleted from chromosome 10 (PTEN) gene, which is also known as mutated in multiple advanced cancers (MMAC1) and transforming growth factor beta (TGF-β) regulated and epithelial cell-enriched phosphatase (TEP1), is an important tumor suppressor gene located at 10q23–24 (Robertson et al., 1998a; Wu et al., 2003). PTEN is a unique 55 kDa dual specificity phosphatase dephosphorylating phosphoserine and phosphotyrosine residues in proteins (Lee et al., 1999; Maehama and Dixon, 1999; Waite and Eng, 2002). It is also a lipid phosphatase hydrolyzing the secondary messenger phosphatidylinositol 3,4,5-trisphosphate (PIP3) (Gericke et al., 2006; Maehama and Dixon, 1999). Structurally, it is the N-terminal phosphatase domain of PTEN from amino acids 22–185 that catalyzes the hydrolysis of phospholipids. The central C2 lipid binding domain from amino acids 190–351 and C-terminal PSD95, DlgA, Zo-1 (PDZ) ligand sequence from amino acids 401–403 are associated with binding to the lipid (Gericke et al., 2006; Miller et al., 2002; Tamguney and Stokoe, 2007). PTEN also contains the characteristic protein phosphatase signature sequence “HCKAGKGR” spanning amino acids 123–130 (Figure 1A) (Maehama et al., 2004). This signature sequence also contains two lysine residues that are key for establishing interactions with negatively charged PIPs (Maehama et al., 2004).

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Figure 1.  Structure of the PTEN and Akt3 proteins. (A) PTEN, a tumor suppressor protein and lipid phosphatase, is a 55 kDa enzyme containing an N-terminal phosphatase domain, a central C2 domain, and a C-terminal tail. Each domain has sites for post-translational modifications that involve: acetylation, oxidation, ubiquitination, or phosphorylation, which have potential to regulate PTEN activity. (B) Structural analysis of Akt3 reveals that this oncogenic survival kinase increasingly active during melanoma progression consists of an N-terminal pleckstrin homology (PH) domain, a central kinase domain and a C-terminal regulatory motif. Complete activation of this kinase occurs only when the threonine 308 (T308) and serine 472 (S472) gets phosphorylated by phosphoinositide-dependent kinase-1 (PDK1) and a PDK2.

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Although, PTEN exhibits both protein and lipid phosphatase activities, it is the lipid phosphatase activity that is generally thought to be the major function of this phosphatase (Maehama and Dixon, 1999; Waite and Eng, 2002). The PTEN active site is structurally designed to facilitate electrostatic interactions with PIP3 for binding and hydrolysis (Lee et al., 1999). As a protein phosphatase, PTEN can dephosphorylate focal adhesion kinase, regulating cell-to-cell adhesion and the Src homologous and collagen gene (an adaptor protein) to disrupt cell spreading and migration. PTEN can also suppress MAPK signaling activity to modulate cell-to-cell adhesion and migration (Li and Ross, 2007; Waite and Eng, 2002; Wu et al., 2003). In its role as a lipid phosphatase, PTEN removes a phosphate group at the third position from cellular PIP3 and phosphatidylinositol 3,4-bisphosphate (PIP2) thereby decreasing the activities of several proteins or pathways whose activities are regulated by this lipid thereby modulating cell proliferation, survival, and apoptosis (Mikhail et al., 2005; Wu et al., 2003).

PTEN-null embryonic fibroblasts have elevated levels of PIP3 leading to constitutive Akt activity, which demonstrates that PTEN regulates the Akt pathway (Dahia et al., 1999; Wu et al., 1998a). PTEN is essential for murine embryonic development beyond day 7.5 (Di Cristofano et al., 1998) and loss of a single PTEN allele leads to hyperplasia and dysplasia in the skin, gastrointestinal tract, and prostate, as well as tumor formation (Di Cristofano et al., 1998). PTEN protein is also absent or functionally inactivated in many different tumor types causing increased Akt activation (Dahia et al., 1999; Wu et al., 1998b). PTEN expression in cells can suppress colony formation, growth in soft agar, and tumor formation in nude mice (Cheney et al., 1998).

Regulation of PTEN activity

PTEN expression and activity are regulated at transcriptional and post-translational levels (Gericke et al., 2006; Mirmohammadsadegh et al., 2006; Robertson et al., 1998a). Alterations in PTEN promoter activity have been shown to modulate cellular protein levels in response to positive and negative regulators (Gericke et al., 2006; Maehama et al., 2004). Some of the positive regulators of PTEN promoter activity include EGR-1 (early growth regulated transcription factor), PPARγ (peroxisome proliferator-activated receptors) and p53 (Gericke et al., 2006). Negative regulators such as mitogen-activated protein kinase-4 (MKK-4), NFκB (nuclear factor kappa-light-chain-enhancer of activated B-cells), TGF-β, and c-JUN have been shown to inhibit PTEN protein expression in several cancers (Gericke et al., 2006; Lopez-Bergami et al., 2008; Wu et al., 2003). Although, these pathways have been demonstrated to regulate melanoma development, detailed mechanisms by which they inhibit PTEN activity remain to be established.

PTEN activity is also modulated by interaction with lipids and proteins. Recently, protein interacting with the C-tail-1 (PICT-1) has been shown to interact with the C-tail of PTEN thereby regulating its turnover (Gericke et al., 2006; Tamguney and Stokoe, 2007). SiRNA-mediated down regulation of PICT-1 protein levels led to destabilization of PTEN and decreased protein levels. Aberrant PICT-1 mRNA levels have been reported in human gliomas, neuroblastomas and ovarian carcinomas (Tamguney and Stokoe, 2007). However, its expression and activity patterns in melanomas are yet to be studied.

Post-translational modifications such as phosphorylation, oxidation, acetylation, and ubiquitination can also regulate the activity of this phosphatase (Figure 1A) (Gericke et al., 2006; Miller et al., 2002; Tamguney and Stokoe, 2007). The oxidation of cysteine residues C71 and C124 by reactive oxygen species inhibits the phosphatase activity of PTEN. Acetylation is another mechanism by which PTEN activity is negatively regulated in many cancer cell types. The histone acetyltransferase p300/CBP-associated factor (PCAF) acetylates lysine residues 125 and 128 (located within the catalytic cleft) of PTEN thereby decreasing affinity towards PIP3’s. PCAF regulates melanoma development by acetylation, thereby stabilizing NFκB in the nucleus (Ueda et al., 2007). Regulation of PTEN activity by PCAF in melanomas warrants investigation.

Phosphorylation of the C-terminal tail of PTEN has been found to regulate PTEN activity. The C-terminal tail of PTEN contains multiple serine and threonine residues (S362, T366, S370, S380, T382, T383, and S385), which can be phosphorylated (Figure 1A) (Miller et al., 2002; Tamguney and Stokoe, 2007). Amino acids S370 and S385 are phosphorylated by casein kinase-2 (CK2). Recently, other kinases such as LKB1, Src, glycogen synthase kinase GSK3β have also been shown to play a role in PTEN phosphorylation (Gericke et al., 2006; Tamguney and Stokoe, 2007). Phosphorylated PTEN is stable but less active compared with unphosphorylated PTEN, which is less stable (Dahia, 2000; Gericke et al., 2006). C-tail mutants of PTEN, including deletions and missense mutations, tend to be short lived. A deletion of the C-terminal 18 amino acids has been shown to completely destabilize PTEN protein. Furthermore, amino acid substitutions at L345 or T348 to L345Q and T348I, respectively, produce highly unstable proteins, contributing to ∼20% of known tumor-associated PTEN mutations (Dahia, 2000; Maehama et al., 2004; Tamguney and Stokoe, 2007). It is uncertain whether these occur in melanoma.

The subcellular distribution of PTEN is a further key to its activity and may play a role in cancer development (Gericke et al., 2006; Wu et al., 2003). C-tail phosphorylation can influence translocation of PTEN to the cell membrane. Kinases such as CK2 and GSK3β have been shown to phosphorylate PTEN thereby decreasing its association with the cell membrane (Al-Khouri et al., 2005; Gericke et al., 2006). Cytosolic PTEN is inactive but highly stable. PTEN has intrinsic membrane translocation signals in the phosphatase and C2 domains. Mutations in these regions impair its ability to translocate to the plasma membrane. Additionally, PTEN localization and stability were regulated by interaction with other proteins (Dahia, 2000; Gericke et al., 2006; Tamguney and Stokoe, 2007). For example, monoubiquitination of PTEN promotes nuclear localization whereas polyubiquitination causes the protein to remain in the cytosol. Ubiquitination of PTEN is catalyzed by neural precursor cell expressed, developmentally down-regulated 4 (NEDD4) and NEDD1 (Kim et al., 2008; Wang et al., 2007b). However, whether similar ubiquitination patterns occur in melanomas needs investigation.

Finally, genetic and epigenetic mechanisms such as promoter methylation, mutations, chromosomal deletions, and expression of endogenous microRNAs have also been shown to modulate the expression and activity of this important phosphatase (Gericke et al., 2006; Waite and Eng, 2002). Genetic mechanisms regulating PTEN expression are: (i) loss of the whole chromosome, (ii) homozygous deletion, (iii) frameshift or point mutations, and (iv) inframe deletion and truncation (Li and Ross, 2007; Yin and Shen, 2008). Loss of chromosome 10, which contains the PTEN gene, has been reported in several cancers, including ∼30–60% of non-inherited melanomas (Stahl et al., 2003). Furthermore, mutations in the PTEN gene have been shown to be associated with ∼28% of glioblastomas, ∼34% endometrial carcinomas, ∼11.8% prostate cancer and ∼12% melanomas (Yin and Shen, 2008). Mechanistically, loss or inactivation of PTEN leads to Akt activation, which upon induction leads to the phosphorylation and monoubiquitination of DNA damage checkpoint kinase (Chk1), causing genomic instability, double stranded DNA breaks and ultimately, cancer development (Yin and Shen, 2008). Epigenetic modifications of PTEN arise by intrinsic (development, differentiation and cancer) or extrinsic (environmental) factors and can be reversed by chemical or environmental treatment modalities. CpG-rich regions of DNA, also known as CpG islands, which are distributed throughout the whole genome, have been shown to undergo methylation in several cancers including melanoma (Costello et al., 2000; Furuta et al., 2004; Wu et al., 2003). DNA methylation is a well-studied epigenetic mechanism for silencing of PTEN in melanoma (Furuta et al., 2004; Liu et al., 2008; Mirmohammadsadegh et al., 2006).

MicroRNAs are small non-coding RNAs of ∼22 nucleotides long (Wang and Lee, 2009). Recent studies have shown that microRNAs can negatively regulate gene expression at the post-transcriptional and/or translational level in different cell types (Wang and Lee, 2009). MicroRNAs targeting PTEN gene expression have been identified in several cancers (Huang et al., 2009; Pezzolesi et al., 2008; Yang et al., 2008). miR-214 has been shown to regulate PTEN translation by binding to its 3′-UTR, which in turn leads to Akt activation and chemoresistance in human ovarian cancers (Yang et al., 2008). In a different study, miR-21 has been demonstrated to cause hepato-cellular carcinoma by inhibiting PTEN expression (Meng et al., 2007). However, microRNAs regulating PTEN expression in melanoma have not yet been identified. As melanomas are highly resistant to chemotherapies and currently no treatment options are available for combating the advanced stage disease, identification of microRNAs regulating PTEN expression has significant potential to lead to novel therapeutic interventions.

The Akt family as oncogenes

The Akt kinase family consists of three protein kinases Akt1 (PKBα), Akt2 (PKBβ), and Akt3 (PKBγ) (Brazil et al., 2002; Nicholson and Anderson, 2002). Akt isoforms share >80% amino acid homology, containing three structurally distinct functional domains (Bellacosa et al., 2004; Brazil and Hemmings, 2001; Brazil et al., 2002, 2004; Datta et al., 1999; Nicholson and Anderson, 2002; Scheid and Woodgett, 2001, 2003; Testa and Bellacosa, 2001) (Akt3 shown in Figure 1B). The N-terminal pleckstrin homology domain spans amino acids 1–107, mediating protein–protein and protein–lipid interactions (Ferguson et al., 2000; Lietzke et al., 2000). The central catalytic domain contains a threonine residue (T305) whose phosphorylation is essential for activating this protein (Andjelkovic et al., 1995; Jones et al., 1991). The carboxy terminal tail region, known as the regulatory domain, contains a second phosphorylation site serine (S472). Phosphorylation of this second site is required for complete Akt3 activation (Figure 1B). In response to growth factors or other extracellular stimuli both sites become phosphorylated, resulting in the complete activation of Akt isoforms (Alessi et al., 1996). Other possible phosphorylation sites may also be important and research in this area continues (Alessi et al., 1996). Splice variants of Akt3 lacking serine 472 have been identified but the significance of this form remains unknown (Brodbeck et al., 2001; Konishi et al., 1995).

Regulation of Akt activity

Activity of the Akt isoforms is regulated through similar mechanisms, but activity of a particular isoform is cell type dependent (Bellacosa et al., 2004; Brazil and Hemmings, 2001; Brazil et al., 2002, 2004; Datta et al., 1999; Nicholson and Anderson, 2002; Scheid and Woodgett, 2001, 2003; Testa and Bellacosa, 2001). In normal cells, growth factors bind to a cell surface receptor or through G-protein-coupled receptors, activating PI3K as shown in Figure 2 (Burgering and Coffer, 1995; Franke et al., 1995). Active PI3K then phosphorylates PIP2 on the 3-OH group generating the second messenger PIP3 (Vanhaesebroeck and Alessi, 2000). PIP3 does not activate Akt directly, but rather promotes Akt translocation to the plasma membrane, where altered conformation of the protein mediated by PIP3 binding allows subsequent phosphorylation by phosphoinositide-dependent kinase-1 (PDK-1).

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Figure 2.  Phosphoinositide 3-kinase (PI3K) and mitogen-activated protein kinase (MAPK) signaling interactions in melanoma. PI3 and MAP kinase signaling cascades regulate cell senescence, proliferation and apoptosis. Whereas the Ras/Raf/Mek/Erk signaling arm is primarily involved in controlling proliferation, high levels of activity can induce cell senescence in benign nevi to inhibit further progression into melanomas. The survival kinase Akt3 inhibits apoptosis and induces proliferation by phosphorylation of substrate proteins. Recently, Akt3 has been shown to inhibit V600EB-Raf activity by phosphorylation thereby promoting early melanoma development by lowering activity of the MAP kinase pathway to levels that promote rather than inhibit growth.

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Akt3 activity is regulated by phosphorylation at threonine 305 and serine 472 (Figures 1B and 2). Phosphorylation at threonine 305, which is mediated by PDK1, partially activates Akt3, but full activation also requires phosphorylation of serine 472 (Alessi et al., 1996). Mechanism mediating serine 472 phosphorylation on Akt3, though controversial, is suspected to involve a second PDK, called PDK2; the identity of this factor remains unclear (Chan and Tsichlis, 2001). Integrin-linked kinase (ILK) and mammalian target of rapamycin complex-2 (mTORC2) can phosphorylate serine 472. However, studies have shown that ILK only acts as a facilitator; leaving mTORC2 as the PDK2 candidate (Alessi et al., 1996; Delcommenne et al., 1998). PDK2 activity of the mTOR complex has been recently established but in melanomas its role in maintaining Akt3 phosphorylation has not been studied (Feldman et al., 2009; Huang and Manning, 2009). Akt autophosphorylation might also play a role in the activation process (Bellacosa et al., 2004; Brazil and Hemmings, 2001; Brazil et al., 2002, 2004; Datta et al., 1999; Nicholson and Anderson, 2002; Scheid and Woodgett, 2001, 2003; Testa and Bellacosa, 2001). Thus, basal Akt activity in a cell depends upon a balance between positive signals from elevated PIP3 levels and negative signals leading to Akt dephosphorylation and inactivation. As this review focuses on Akt signaling in melanoma, subsequent sections discuss what is known about Akt3 deregulation in melanomas and the signals that regulate its activity.

PTEN and AKT3 in human melanomas

  1. Top of page
  2. Summary
  3. Introduction
  4. PTEN and AKT3 in human melanomas
  5. Cellular processes regulated by PTEN/Akt3 signaling in melanomas
  6. Therapeutic potential of targeting the PTEN/Akt3 signaling cascade in melanomas
  7. Conclusions
  8. Key unanswered questions
  9. Acknowledgements
  10. References

PTEN is a key phosphatase regulating melanoma development

PTEN is a tumor suppressor inhibiting melanoma cell growth by increasing susceptibility of cells to apoptosis (Lu et al., 1999; Weng et al., 1999). Adenovirus-mediated transfer of PTEN into melanoma cells containing wild-type PTEN alleles led to inhibition of phosphorylated (active) Akt, increasing apoptosis and reducing growth rates (Stewart et al., 2002), which demonstrated the importance of this protein in melanoma (Figure 3A,B). PTEN loss preferrentially regulates Akt3 activity in melanoma (Stahl et al., 2004). SiRNA-mediated reduction of PTEN specifically increased Akt3 phosphorylation (activity) in melanocytes and early stage melanoma cells (WM35) expressing wild-type PTEN protein, thereby reinforcing the significance of Akt3 involvement in melanoma development (Figure 4) (Stahl et al., 2004).

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Figure 3.  PTEN regulates apoptosis by inhibiting Akt activity in melanomas. (A) PTEN expression decreases pAkt levels in melanoma cells lacking functional PTEN. UACC 903 melanoma cells lacking functional PTEN protein were infected with increasing amounts (7.8, 15.6, 31.3, 62.5, 125 μL) of adeno-associated viral constructs containing wild type PTEN, HA tagged wild type PTEN and a catalytically inactive G129R PTEN mutation. Three days later, cell lysates were collected and proteins analyzed by Western blotting. Levels of pAkt and total Akt were quantitated by densitometry and the pAkt/totalAkt ratio represented against amount of viral supernatant used for infection. Data show that pAkt expression decreases with increasing virus amount indicating PTEN reduces pAkt in melanomas (Stahl et al., 2003). (B) PTEN triggers apoptosis in melanomas. Levels of cleaved caspase-3, an indicator of apoptosis, were measured using Western blotting following expression of viral introduced PTEN into UACC 903 melanoma cells lacking functional PTEN protein. Compared with functionally inactive G129R PTEN, wild-type PTEN expression increased levels of cleaved caspase-3 indicating elevated levels of apoptosis. α-enolase served as control for protein loading (Stahl et al., 2003).

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Figure 4.  PTEN loss leads to preferential increase in Akt3 activity in melanocytes and radial growth phase melananoma cells. Normal human melanocytes and a cell line derived from a radial growth phase of melanoma (WM35) that contain low pAkt levels were transfected with siRNA targeting PTEN and/or one of the isoforms of Akt. A significant decrease in pAkt was noticed only when PTEN and Akt3 were targeted together but not with either PTEN and Akt1 or PTEN and Akt2, indicating that Akt3 is activated preferentially following PTEN loss (Stahl et al., 2004).

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The growth-suppressive effects of PTEN were significant enough to cause fragmentation of a normal copy of chromosome 10 introduced into melanoma cell line UACC 903 that lacks PTEN protein because of the presence of a truncating point mutation (Robertson et al., 1998b). The introduction of a normal chromosome 10 containing wild-type PTEN into UACC 903 cells reduced the cellular growth potential, causing fragmentation of the introduced chromosome to eliminate the growth-suppressive effects mediated by PTEN. The introduced chromosome 10 underwent deletion, which mirrored alterations occurring in tumors from melanoma patients leading to identification of PTEN as the cause of this phenomenon (Thompson et al., 1995). It was this observation that led to the functional identification of PTEN as the suppressor gene on the long arm of chromosome 10 important in melanoma, which was subsequently validated through identification of a point mutation truncating the protein in the cell line preventing protein production (Robertson et al., 1998b). Expression of wild-type PTEN in these cells, reduced cell growth and increased sensitivity of cells to apoptotic stimuli (Robertson et al., 1998b). Similar reports have confirmed that expression of PTEN in cell lines lacking the protein, reduce levels of phosphorylated Akt and downstream substrates such as GSK3β and proline rich Akt substrate of 40 kDa (PRAS40) (Davies et al., 1998; Li et al., 1998; Madhunapantula et al., 2007).

Ectopically expressing PTEN protein can inhibit invasion and induce apoptosis in melanoma cells (Stahl et al., 2003; Stewart et al., 2002). Cells lacking functional PTEN protein expression exhibited increased BCl2 activity, resistance to growth factor receptor inhibitors and chemotherapeutic agents as well as having had a growth advantage compared with those expressing physiological levels of the protein (Madhunapantula et al., 2007; Mikhail et al., 2005; Stahl et al., 2003, 2004). Furthermore, decreased PTEN activity alters cell cycle progression, migration and adhesion of melanoma cells making it an important regulator of melanoma development (Wu et al., 2003). Recently, PTEN loss and V600EB-Raf has been shown to cooperate to promote metastatic melanoma development (Dankort et al., 2009). A mouse model, expressing V600EB-Raf at physiological levels in combination with PTEN loss, led to tumor development, further validating the important role of PTEN in melanoma development (Dankort et al., 2009).

PTEN inactivation either by phosphorylation or oxidation of cysteine residues increases the tumorigenicity of tumor cells (Gericke et al., 2006; Tamguney and Stokoe, 2007). Introduction of the PTEN gene into melanoma cells lacking functional protein, inhibited cell survival by decreasing activity of Akt3 and downstream pPRAS40 levels (Madhunapantula et al., 2007; Stahl et al., 2003, 2004). Low intracellular levels of pAkt and pPRAS40 induce cellular apoptosis mediated through caspases (Madhunapantula et al., 2007). Comparing isogenic PTEN-null variants of the UACC 903 melanoma cells to PTEN containing cells, demonstrated that PTEN sensitized the melanoma cells to chemotherapeutic agents and apoptosis inducers such as staurosporine (Gaitonde et al., 2009; Madhunapantula et al., 2007; Stahl et al., 2004).

Mechanisms leading to PTEN inactivation in melanomas

Several studies have identified loss of the chromosome 10q23 region containing the PTEN gene in melanomas (Poetsch et al., 2001b; Robertson et al., 1999a; Wu et al., 2003). Screening of melanoma cell lines and paired uncultured metastatic melanoma and peripheral blood specimens for PTEN loss and/or alterations using PCR and direct sequencing found ∼30–40% melanoma cell lines containing homozygous deletions (including intragenic loss) while 9% had nonsense, frame shift, and intronic mutations. However, only ∼5–15% of uncultured melanoma specimens contained nonsense mutations or homozygous deletions (Tsao et al., 1998a; Yin and Shen, 2008). Intragenic polymorphisms in introns have also been reported to regulate PTEN expression in melanomas. Amino-acid altering mutations (P95S, F154L, L325F) induced by UV radiation (UVB and UVA) have been shown to impair PTEN function and thereby promote the development of early melanomas in patients suffering from xenoderma pigmentosum (Wang et al., 2009).

PTEN is generally accepted to be lost early in melanoma development. Melanoma patient tumor material commonly has decreased PTEN expression, mediated through loss of a single copy of chromosome 10 (Bastian et al., 1998; Mertens et al., 1997; Parmiter et al., 1988; Thompson et al., 1995; Wu et al., 2003). Early melanocytic lesions frequently have loss of one allele of PTEN, or PTEN haplo-insufficiency occurring because of loss of the entire chromosome 10 (Bastian et al., 1998; Mertens et al., 1997; Parmiter et al., 1988; Thompson et al., 1995; Wu et al., 2003). In this scenario, chromosome 10 loss reduces PTEN expression in a sub-population of evolving melanoma cells, causing increased Akt3 activation, which provides these cells with a growth and survival advantage (Figures 4 and 5). This is demonstrated in studies showing that growth factors, such as stem cell factor (SCF) strongly activate Akt, which protects melanocytes from TNF-related apoptosis-inducing ligand (TRAIL) and staurosporine-mediated cell death (Larribere et al., 2004). Furthermore, Akt inhibition blocks the antiapoptotic effect of SCF, with only sustained Akt activation protecting melanocytes from apoptosis (Larribere et al., 2004). Thus, decreased PTEN levels because of haplo-insufficiency play an important role in early melanomas by specifically increasing Akt3 activity thereby protecting these cells from apoptosis (Figures 4 and 5).

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Figure 5.  Akt3 expression and activity increase during melanoma development. (A) Expression of pAkt in nevi, dysplastic nevi, primary and metastatic melanoma lesions was quantitated from histological sections and intensity scored using immunohistochemical staining. Compared with common nevi that had only weak-to-moderate pAkt staining, increasing percentages of dysplastic nevi, primary and metastatic melanomas contained higher levels of Akt activity with 67% of advanced tumors having elevated activity (Stahl et al., 2004). (B) Expression and activity of Akt isoforms (Akt1, Akt2 and Akt3) was measured in flash frozen melanoma patient tumor samples by Western blotting. Approximattely 60% of melanoma tumors expressed elevated levels of Akt3 protein compared with normal human melanocytes. Furthermore, ∼43% of tumor had elevated Akt3 activity (Stahl et al., 2004).

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PTEN promoter methylation leading to inactivation of transcription has been found to occur in ∼62% of metastatic melanoma patients (Birck et al., 2000; Boni et al., 1998; Celebi et al., 2000; Guldberg et al., 1997; Poetsch et al., 2001a; Reifenberger et al., 2000; Robertson et al., 1998b; Tsao et al., 1998b, 2000). Quantitative positional methylation analysis and Taqman RT-PCR of 37 sera from melanoma patients and 21 pairs of corresponding sera and melanoma specimens demonstrated that 62% of metastatic melanoma patient’s sera had elevated PTEN promoter methylation (Mirmohammadsadegh et al., 2006). However, contradictory to this observation, the most recent studies by Liu et al., 2008 and Bonazzi et al., 2009 found no DNA methylation in PTEN gene (Bonazzi et al., 2009; Liu et al., 2008). Therefore, although the regulation of PTEN expression by DNA methylation appears to be important, further studies are warranted to measure its contribution to melanoma development. If mutational and epigenetic silencing studies of PTEN were added together, functional inactivation might be involved in upto 77% of non-familial melanomas (Boni et al., 1998; Pollock and Trent, 2000; Saida, 2001; Zhou et al., 2000). It is currently unknown whether direct phosphorylation leading to inactivation of PTEN has any role in silencing of this phosphatase in melanoma (Miller et al., 2002).

Akt3 plays a key role in melanoma development

Loss of PTEN in melanomas promotes Akt3 activity by increasing the cellular levels of PIP3 (Robertson, 2005; Stahl et al., 2003, 2004). Accumulating PIP3 molecules then binds to the pleckstrin homology (PH) domains of Akt3 to facilitate membrane translocation and phosphorylation (Fayard et al., 2005; Sale and Sale, 2008; Scheid and Woodgett, 2003). Activated Akt3 (Figure 1A) phosphorylates: (i) GSK3β serine 9 (S9) to inhibit its activity thereby promoting cell cycle progression through increased cyclin D levels (Fresno Vara et al., 2004; Woodgett, 2005); (ii) PRAS40 at threonine 246 (T246) to inhibit interactions with mTORC1 thereby increasing the nutrient status of the cells (Kovacina et al., 2003; Madhunapantula et al., 2007; Wang et al., 2007a); (iii) V600EB-Raf to decrease its activity to levels that promote rather than inhibit cell proliferation (Cheung et al., 2008; Ikenoue et al., 2005); and (iv) osteopontin, a glycophosphoprotein promoting melanoma progression levels to a highly metastatic state (Packer et al., 2006) (Figure 2). Furthermore, Akt3 inhibits cellular apoptosis by decreasing caspase-3/7 activity (Sharma et al., 2009; Stahl et al., 2004). Decreased apoptosis makes melanoma cells less sensitive to chemotherapeutic agents functioning through this mechanism.

Akt1 and Akt2 are ubiquitously expressed in most normal tissues compared with Akt3 whose expression is restricted (Bellacosa et al., 2004; Brazil and Hemmings, 2001; Brazil et al., 2002, 2004; Datta et al., 1999; Nicholson and Anderson, 2002; Scheid and Woodgett, 2001, 2003; Testa and Bellacosa, 2001). However, expression does not necessarily imply activity of a particular isoform (Bellacosa et al., 2004; Brazil and Hemmings, 2001; Brazil et al., 2002, 2004; Datta et al., 1999; Nicholson and Anderson, 2002; Scheid and Woodgett, 2001, 2003; Stahl et al., 2004; Testa and Bellacosa, 2001). Activity of a particular isoform is cell type-dependent relying on a balance between signals promoting or inhibiting activity. This is the case for melanomas where all three isoforms are expressed but Akt3 is the predominantly active isoform (Figure 5). Increased Akt3 expression/activity occur in 60–70% of sporadic melanomas demonstrating a key role in melanoma development (Figure 5) (Dhawan et al., 2002; Stahl et al., 2004).

Increased Akt3 activation also plays a significant role in progression to more advanced aggressive tumors (Madhunapantula et al., 2007; Robertson, 2005; Stahl et al., 2004). An experimental tumor progression model in which Akt3 activity in melanocytes was compared with low passage cell lines from primary melanoma tumors at the radial and vertical stages of cell growth, revealed that Akt3 activity increased in the radial growth phase and remained elevated in comparison to Akt1 and Akt2. The high level of involvement in advanced melanomas leads to the inference that Akt3 activation performs critical functions in melanoma development (Robertson, 2005; Stahl et al., 2004).

Mechanism promoting Akt3 deregulation in melanomas

Akt3 plays an important role in signaling pathways that regulate the tumorigenic processes (Nicholson and Anderson, 2002; Testa and Bellacosa, 2001). It is unknown why Akt3 and not the other isoforms are activated in melanomas. However, it is known that loss of functional PTEN in melanocytes, leads to preferential activation of Akt3 (Figure 4) (Robertson, 2005). Increased copy numbers of the Akt3 gene in melanomas, does not alone account for preferential Akt3 activation (Stahl et al., 2004; Wu et al., 2003). Akt3 activation may involve preferential interaction of PIP3 and/or accessory protein interaction with the PH domain (Bellacosa et al., 2004; Brazil and Hemmings, 2001; Brazil et al., 2002, 2004; Datta et al., 1999; Nicholson and Anderson, 2002; Scheid and Woodgett, 2001, 2003; Testa and Bellacosa, 2001), which is where PIP3 lipid–protein interactions occur (Figure 1B). The isoforms have different phosphorylation sites within the PH domain having as yet uncharacterized functions (Bellacosa et al., 2004; Brazil and Hemmings, 2001; Brazil et al., 2002, 2004; Datta et al., 1999; Nicholson and Anderson, 2002; Scheid and Woodgett, 2001, 2003; Testa and Bellacosa, 2001). A precedent exist to support this possibility; a ceramide induced, PKC zeta-dependent phosphorylation site at threonine 34 (T34) has been identified that leads to Akt1 inactivation by preventing binding to PIP3 (Powell et al., 2003). At this site Akt2 and Akt3 have a serine. Thus, differential regulation of putative phosphorylation sites within the PH domain of Akt3 may provide the basis for the specificity of Akt3 activation in melanomas. Preferential Akt3 interactions with other proteins could also lead to selective regulation in melanomas. T-cell leukaemia/lymphoma-1 (TCL1) selectively binds to the Akt3 PH domain, thereby promoting hetero-oligomerization of Akt1 with Akt3, causing transphosphorylation of Akt in leukemias (Laine et al., 2000, 2002; Pekarsky et al., 2000). Thus, factors interacting preferentially with Akt3 may lead to selective activation in melanomas (Bellacosa et al., 2004; Brazil and Hemmings, 2001; Brazil et al., 2002, 2004; Datta et al., 1999; Nicholson and Anderson, 2002; Scheid and Woodgett, 2001, 2003; Testa and Bellacosa, 2001).

Akt activation starts with upstream PI3K in this cascade, which is activated as a result of ligand-dependent activation of tyrosine kinase receptors, G-protein-coupled receptors, or integrins (Figure 2) (Blume-Jensen and Hunter, 2001). Many of theses ligands are overexpressed in cancers, making this a route for Akt activation in melanomas (Nicholson and Anderson, 2002; Testa and Bellacosa, 2001). Another possibility involves overexpression or constitutive activation of cell surface receptors, which are reported in melanomas (Blume-Jensen and Hunter, 2001; Polsky and Cordon-Cardo, 2003). Receptor-independent activation also occurs in 10–20% melanomas expressing constitutively active Ras proteins (Kauffmann-Zeh et al., 1997; Polsky and Cordon-Cardo, 2003; Rodriguez-Viciana et al., 1997). Elevated PI3K activity itself can also cause Akt activation. Chromosome 3q26 containing the p110 catalytic subunit of PI3K, which is frequently amplified in cancer of the ovary (Shayesteh et al., 1999) and cervix (Ma et al., 2000), leading to increased PI3K catalytic activity. The importance of PI3K signaling in melanoma was demonstrated by over expressing a deleted subunit of PI3K (Deltap85) to reduce PI3K signaling (Tachiiri et al., 2000). In this manner, Delta p85 functioned as a dominant-negative disrupting p85/p110 subunit interaction, consequently inducing apoptosis in the melanoma cell line G361. Inhibiting Akt signaling in tumor cells by adenoviral transfer of a Akt kinase-dead mutant, in which the two regulatory phosphorylation sites have been mutated to alanines thereby converting it to a dominant-negative, led to selective induction of apoptosis in tumor cells expressing activated Akt (Jetzt et al., 2003). By contrast, a minimal effect was observed in normal or tumor cells expressing low levels of active Akt (Jetzt et al., 2003). These studies validate the importance of Akt activation in tumor cell survival.

A key mechanism for increased Akt activity in cancer cells involves genetic amplifications or mutations leading to constitutive activation. Recently, a low frequency activating mutation (E17K) in the pH domain of Akt3 has been identified in melanoma cell lines and ∼4% of patient tumors (Davies et al., 2008). This mutation enables Akt3 to get recruited to cell membranes independent of PI3K, which leads to cellular transformation. Genetic amplifications increasing Akt1 or Akt2 expression occur in carcinomas of the stomach, ovary, pancreas, and breast (Bellacosa et al., 1995a,b; Cheng et al., 1992, 1996a,b; Lu et al., 1995; Staal, 1987; Van Dekken et al., 1999). Specifically, Akt2 amplification occurs as part of the 19q13.1–q13.2 amplicon in high-grade aggressive ovarian tumors (Thompson et al., 1996). Even though no amplifications of Akt genes have been reported in melanomas (Waldmann et al., 2001, 2002), Akt3 protein is frequently overexpressed (Stahl et al., 2004), as a result of copy number increases of the long arm of chromosome 1 containing the gene (Bastian et al., 1998; Mertens et al., 1997; Thompson et al., 1995). No increases in the long arms of chromosome 14 or 19 containing the Akt1 and Akt2 genes, respectively, have been reported (Bastian et al., 1998; Mertens et al., 1997; Thompson et al., 1995). Thus, increase in Akt3 copy number is a mechanism contributing to increased expression and activity in melanoma. However, expression does not necessarily imply activity as observed with Akt1 and Akt2 expression but little activity in melanomas (Stahl et al., 2004). Therefore, other processes must also contribute to Akt3 activation.

Inactivation of negative regulators of Akt provides another mechanism to regulate Akt activity (Cantley and Neel, 1999b). Akt phosphatases that directly dephosphorylate Akt may play a role in this process as can be observed when treating cells with inhibitors of protein serine/threonine phosphatases, such as okadaic acid (Andjelkovic et al., 1996). While the identity of these phosphatases remains uncertain, PP2A phosphatase may be involved in this process (Andjelkovic et al., 1996). Proteins binding to Akt also have the potential to modulate cellular activity as is observed with the protooncogene TCL1, which enhances oligomerization of Akt1 with Akt3, thereby facilitating activation of Akt3 in leukemia (Laine et al., 2000, 2002; Pekarsky et al., 2000). Another example is the heat shock protein 90 (Hsp90) that can complex with Akt. Inhibition of Akt–Hsp90 complex formation can inactivate Akt by PP2A-mediated dephosphorylation (Fujita et al., 2002; Sato et al., 2000). While none of these interactions have been studied in melanoma, the interested reader can learn more about the proteins interacting with and regulating Akt activation in other reviews; for additional information see reference (Brazil et al., 2004).

Cellular processes regulated by PTEN/Akt3 signaling in melanomas

  1. Top of page
  2. Summary
  3. Introduction
  4. PTEN and AKT3 in human melanomas
  5. Cellular processes regulated by PTEN/Akt3 signaling in melanomas
  6. Therapeutic potential of targeting the PTEN/Akt3 signaling cascade in melanomas
  7. Conclusions
  8. Key unanswered questions
  9. Acknowledgements
  10. References

Cell survival, migration, metastasis and chemoresistance regulated by PTEN/Akt3 signaling

PTEN regulates several processes such as inhibition of cell proliferation by altering cell cycle progression through G1 to S phase and control of apoptosis by modulating Akt activity (Cantley and Neel, 1999a; Li and Ross, 2007; Mikhail et al., 2005; Ramaswamy et al., 1999). Additionally, PTEN expression has been associated with cell–cell adhesion, cell migration, and metastasis (Stewart et al., 2002; Wu et al., 2003). Tumor cells lacking PTEN exhibit unusually high metastatic activity and chemoresistance (Lopez-Bergami et al., 2008; Robertson, 2005; Stahl et al., 2003; Wu et al., 2003). Furthermore, PTEN expression using a variety of vectors or from an introduced chromosome in melanoma cell lines lacking PTEN induced apoptosis (Figure 6A) and inhibited tumor development (Mikhail et al., 2005; Stahl et al., 2003; Stewart et al., 2002). Cells containing functionally active PTEN protein exhibit elevated p27 expression, decreased cyclin-D1 and cyclin-D2 proteins (Huang et al., 2007; Ramaswamy et al., 1999; Wu et al., 2003).

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Figure 6.  PTEN introduction or Akt3 inhibition induce apoptosis in melanomas. Photographs shows TUNEL-positive cells (an indicator of apoptosis) in tumor xenografts following PTEN expression (A) or siRNA-mediated reduction of Akt3 protein levels (B). UACC 903 cells or cells expressing chromosomal PTEN or cells nucleofected with siAkt3 versus siAkt2 (1 × 106) were injected into nude mice and 4 days later processed for TUNEL staining. Data shows that either PTEN expression or Akt3 protein knockdown increased apopotosis compared with controls in which PTEN activity had been lost (revertant) or cells with reduced Akt2 protein levels (Stahl et al., 2004).

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Akt3 has been shown to be a pro-survival kinase in melanomas (Stahl et al., 2004). SiRNA targeting Akt3 protein levels (Figure 6B) or expression of PTEN (Figure 6A) selectively lowers Akt3 activity, thereby reducing the tumorigenic potential of melanoma cells by altering apoptotic sensitivity of the cells (Madhunapantula et al., 2007; Stahl et al., 2004). Furthermore, increased activity correlates with tumor progression, providing cells with a selective advantage in the tumor environment.

Processes such as melanoma tumor progression, metastasis, cell–cell adhesion, cell migration, and development of chemoresistant tumors under hypoxic conditions are also regulated by PI3 kinase and Akt signaling pathways (Dai et al., 2005; Govindarajan et al., 2007; Robertson, 2005). Activated Akt in metastatic melanoma cells have been shown to regulate Notch1 expression via nuclear factor kappa beta (NFκB) thereby promoting tumor development under hypoxic tumor conditions (Bedogni et al., 2008). A different study has shown that Akt inhibits RhoB, a GTPase, in melanomas and thereby induces tumor cell survival, transformation, invasion, and metastasis (Jiang et al., 2004).

Downstream targets in the PTEN/Akt3 signaling cascades

While inactive Akt resides in the cytoplasm, activation occurs at the cell membrane followed by translocation to cytosol and nucleus (Andjelkovic et al., 1997; Borgatti et al., 2000; Dufner et al., 1999; Filippa et al., 2000; Meier et al., 1997). Akt substrates can be cytoplasmic or nuclear proteins and numbers continues to increase as studies such as those using the minimal consensus peptide sequence Arg–X–Arg–X–X–[Ser/Thr]–Hyd (where X is any amino acid and Hyd is a bulky hydrophobic amino acid) search for putative substrates (Alessi et al., 1995; Obata et al., 2000). The functions of many of these substrates in cellular processes have been identified, demonstrating that Akt regulates multiple processes in cells including apoptosis and proliferation (Figure 2). This review does not provide an exhaustive discussion of all Akt substrates, but rather focuses on those currently identified as playing important roles in melanoma development; for additional information regarding Akt substrates see references (Bellacosa et al., 2004; Brazil and Hemmings, 2001; Brazil et al., 2002, 2004; Datta et al., 1999; Nicholson and Anderson, 2002; Scheid and Woodgett, 2001, 2003; Testa and Bellacosa, 2001).

Substrates for Akt3 do not appear to be specific but rather seem to be identical to those acted on by all three Akt isoforms. Several substrates have been identified as being important in melanoma development. First, a switch from E- to N-cadherin in melanoma has been shown to promote cell survival by activating the Akt pathway, resulting in inactivation of BAD protein and accumulation of steady state levels of β-catenin (Li et al., 2001). Second, melanoma cell activity has been linked to enhanced NFκB nuclear localization and transactivation and inhibition of Akt activity led to increased apoptosis and decreased NFκB promoter activity (Dhawan et al., 2002). Third, Akt has been shown to enhance human telomerase activity through phosphorylation of human telomerase reverse transcriptase (hTERT) subunit (Kang et al., 1999). Inhibition of Akt reduced hTERT peptide phosphorylation and telomerase activity (Kang et al., 1999). Fourth, Akt phosphorylates serine 71 of Rac1 thereby modulating the Rac1 signal transduction pathway in SK-MEL-28 melanoma cells (Kwon et al., 2000). Fifth, activated Akt upregulates MelCAM while overexpression of MelCAM activated endogenous Akt inhibiting the proapoptotic BAD protein (Figure 2) (Li et al., 2003).

Substrates specifically regulated by Akt3 have also been studied and role in melanoma development studied (Figure 2). Recently, Akt3 has been reported to phosphorylate V600EB-Raf on S364 and/or S428 to reduce its activity to levels that promote rather than inhibit melanoma development from melanocytes (Figure 7 kindly provided by Dr. M. Cheung) (Cheung et al., 2008). Ectopic expression of V600EB-Raf in primary cell lines such as melanocytes has been shown to induce cellular senescence not only by elevating the levels of MAPK activity for unusually longer periods but also by upregulating the expression of cyclin-dependent kinase (cdk) inhibitors (Houben et al., 2009; Wajapeyee et al., 2008). Therefore, genetic changes such as loss of tumor suppressor genes (PTEN, p53 or p16INK4A), or upregulation of cooperating oncogenes is necessary to progress into advanced metastatic stages (Dankort et al., 2009; Zhao et al., 2008). Acquisition of Akt3 activity facilitates the progression of quiescent melanocytic nevi into aggressive vertical and metastatic stages by inhibiting V600EB-Raf activity thereby releasing cells from a senescence block (Figure 7). This demonstrates that in melanomas, Akt3 kinase not only increases cell survival but also aids early melanoma development.

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Figure 7.  Akt3 activity promotes melanoma development by inhibiting V600EB-Raf. Akt3 decreases V600EB-Raf activity by phosphorylating the protein thereby decreasing its activity and that of the downstream signaling cascade to levels that promote rather than inhibit melanocyte proliferation, which aids melanoma development.

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Another substrate regulated by Akt3 activity in melanomas involves modulation of apoptosis-mediated through PRAS40 (Figure 2) (Madhunapantula et al., 2007). PRAS40 has been identified as a direct substrate of Akt from a screen conducted using an antibody that recognizes consensus Akt substrate phosphorylation sequence (RXRXX(S/T); and as a 14–3–3 binding protein (Kovacina et al., 2003). Compared with most proteins, PRAS40 contains threetimes more proline residues (5% in most proteins to 15% in PRAS40). PRAS40 is a cytosolic protein found ubiquitously in all eukaryotes (Kovacina et al., 2003) and is phosphorylated by Akt at T246 (Kovacina et al., 2003). pPRAS40T246 protects neuronal cells from ischemic injury by inhibiting caspase-3-mediated apoptotic cell death (Saito et al., 2004). Expression of pPRAS40 levels is also associated with tumor malignancy (Huang and Porter, 2005). Compared with paired control normal cells, cancer cell lines (MCF10A/MCF7, BEAS/H1170) exhibited high pPRAS40 expression (Huang and Porter, 2005). However, the detailed functional characterization, in vitro and in vivo, was not reported. Compared with normal melanocyte controls, 43–60% of flash frozen tumors collected from melanoma patients express high pPRAS40 and pAkt (Madhunapantula et al., 2007). Furthermore, targeted inhibition of PRAS40 using siRNA reduced melanoma tumor growth in xenografted melanoma studies (Figure 8) (Madhunapantula et al., 2007). Mechanistically, PRAS40 inhibition induced caspase-3/7-mediated apoptosis in melanoma cells and increased sensitivity to apoptosis inducers such as staurosporine (Madhunapantula et al., 2007). However, the molecular basis for caspase-3/7 activity inhibition by pPRAS40 in melanomas remains unknown.

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Figure 8.  Knockdown of PRAS40, a substrate of Akt3, inhibits melanoma tumor growth. SiRNA-mediated reduction of PRAS40 protein levels, a direct substrate of Akt, or upstream Akt3 inhibits tumor development in xenografted melanoma tumors. UACC 903 cells were transfected with siRNAs targeting PRAS40 or Akt3, and 1.5 days later cells were injected into nude mice. Developing tumor sizes were measured on alternate days. Compared with buffer, a scrambled siRNA or a siRNA targeting C-Raf, a 50–60% decrease in tumor volume observed following PRAS40 or Akt3 protein knockdown. Inset shows reduction of PRAS40 protein levels in tumors removed from mice at days 7.5 or 9.5 (Madhunapantula et al., 2007).

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Recent reports have demonstrated that PRAS40 is a physiological target of mTORC1 kinase and regulates its activity by functioning as a direct inhibitor of substrate binding (Oshiro et al., 2007; Sancak et al., 2007; Wang et al., 2007a). In insulin-deprived cells, PRAS40 binds to raptor protein via a TOR signaling (TOS) motif thereby inhibiting mTORC1 kinase activity (Fonseca et al., 2007; Wang et al., 2007a). Additionally, it has been shown that in intact cells, mTORC1 phosphorylates PRAS40 at S183 thereby increasing its affinity towards raptor (Fonseca et al., 2007). Therefore, PRAS40 is considered as an inhibitor of cell growth. Supporting this observation, a separate study has reported that siRNA-mediated inhibition of PRAS40 protected HeLa cells from TNFα and cycloheximide-mediated apoptosis (Thedieck et al., 2007). This study concluded that PRAS40 is a pro-apoptotic protein in cells. However, this observation is contradictory to the earlier reports for neuronal cells and melanomas (Huang and Porter, 2005; Madhunapantula et al., 2007). Knocking down PRAS40 using siRNA inhibited melanoma cells growing in culture dishes and xenografted tumor development by triggering apoptosis (Figure 8) (Madhunapantula et al., 2007). Furthermore, targeting Akt using siRNA or pharmacological agents such as isoselenocyanates (ISCs), PBISe, and BI-69A11 decreased pPRAS40 levels and induced caspase-3/7 activity as well as cleaved PARP (Gaitonde et al., 2009; Madhunapantula et al., 2008; Sharma et al., 2009). In cancers such as melanomas, levels of pAkt, hence pPRAS40 are elevated by several fold compared with normal human melanocytes (Huang and Porter, 2005; Madhunapantula et al., 2007). Therefore, increased pPRAS40T246 may release its inhibitory effects on mTORC1 kinase and down-regulate caspase-3/7 activity by yet to be established mechanisms. In conclusion, whereas the phosphorylation of PRAS40 at threonine 246 by Akt is primarily involved in inhibiting cellular apoptosis and increasing survival, the role of unphosphorylated PRAS40 in the cancer cells needs further investigation. Thus, preventing PRAS40 phosphorylation by Akt3 or inhibition of PRAS40 protein expression using siRNAs has significant potential to inhibit melanoma development.

Another well-known substrate of Akt is GSK3 (Figure 2) (Fresno Vara et al., 2004; Robertson, 2005). GSK3 is present in cells as two structurally similar isoforms, known as GSK3α and GSK3β (Patel and Woodgett, 2008). They are serine–threonine protein kinases, involved in regulating diverse cellular processes including cell structure, function, proliferation, and survival (Jope and Johnson, 2004; Ougolkov and Billadeau, 2006). Akt has been shown to phosphorylate S9 of GSK3β and S21 of GSK3α to inhibit their activity thereby promoting cell proliferation by stabilizing cyclin-D1 protein (Fresno Vara et al., 2004; Ramaswamy et al., 1999). In addition, a recent study demonstrated that mouse embryonic fibroblast cells expressing wild type PTEN inhibit cell cycle progression through G1–S phase by down regulating cyclin D2 protein level, which is mediated by GSK3β (Huang et al., 2007). Apart from Akt3, activated Erk also phosphorylate GSK3β on S9 to inhibit its binding to c-Jun thereby increase cell proliferation and survival (Lopez-Bergami et al., 2007). Therefore, unphosphorylated active GSK3 is considered as an apoptosis-inducing tumor suppressor. However, recent studies have shown that GSK3 expression is elevated in advanced cancers and deregulation of GSK3 activity increases malignant transformation of cells (Bellei et al., 2008; Luo, 2009; Ougolkov and Billadeau, 2006; Patel and Woodgett, 2008). In support of these observations, inhibition of GSK3β has been found to enhance sorafenib-induced apoptosis in melanoma cells (Panka et al., 2008). Furthermore, GSK3β inhibition elevated melanogenesis in melanoma cell lines by inducing melanocyte differentiation markers such as melanin synthesis, tyrosinase activity, expression of tyrosinase, and microphthalmia-associated transcription factor (MITF) (Bellei et al., 2008). Furthermore, targeting GSK3β using organometallic inhibitors (DW1/2) decreased Mdm2 activity thereby elevated p53-mediated apoptosis in melanoma cell lines expressing wild type p53 protein (Smalley et al., 2007). Recently, GSK3 has also been shown to maintain the constitutive inhibitory kappaB kinase (IKK) activity and thereby the NFκβ in pancreatic cells (Wilson and Baldwin, 2008). As advanced stage melanomas contain high levels of NFκβ activity compared with melanocytes and early stage melanomas; and expression as well as activity of NFκβ is regulated by PTEN/AKT signaling, the role of GSK3 and its regulation by Akt pathway needs to be more thoroughly investigated (Robertson, 2005; Stahl et al., 2004; Ueda and Richmond, 2006). Finally, GSK3α and not GSK3β have been shown to regulate pancreatic cell survival (Wilson and Baldwin, 2008). Most studies in melanoma suggest that it is GSK3β regulating melanoma development. However, no reports detail percentages of melanoma patient tumors expressing each of these two isoforms and which needs to be targeted for effective tumor inhibition. Future studies should address these issues to better understand GSK3 signaling to design more effective therapeutics for treating melanoma.

Therapeutic potential of targeting the PTEN/Akt3 signaling cascade in melanomas

  1. Top of page
  2. Summary
  3. Introduction
  4. PTEN and AKT3 in human melanomas
  5. Cellular processes regulated by PTEN/Akt3 signaling in melanomas
  6. Therapeutic potential of targeting the PTEN/Akt3 signaling cascade in melanomas
  7. Conclusions
  8. Key unanswered questions
  9. Acknowledgements
  10. References

The potential clinical importance of targeting PTEN or Akt3 in melanomas has been demonstrated by showing that selective inhibition of Akt3 expression (activity) or expression of PTEN significantly reduced melanoma tumor development (Stahl et al., 2004). Therefore, introduction of PTEN into melanoma cells or targeting Akt3 or interfering with regulators of these proteins may represent an effective therapeutic approach for melanoma patients (Johnstone et al., 2002; Soengas and Lowe, 2003). As the vast majority of chemotherapeutic agents induce apoptosis, and expression of PTEN or reduction of Akt3 activity leads to increased sensitivity to apoptotic stimuli, the threshold doses of drugs or radiation required for effective chemo- or radio-therapy could be reduced by targeting these proteins (Soengas and Lowe, 2003). Several studies have demonstrated that targeting these proteins promotes apoptosis and/or increased the sensitivity to chemotherapeutic agents (Bedogni et al., 2004; Ivanov and Hei, 2004; Jetzt et al., 2003; Richmond et al., 2004; Tachiiri et al., 2000). Under these circumstances, introduction of PTEN or decreasing Akt3 activity alone or in combination with chemotherapeutic agents could potentially benefit melanoma patients (Bedogni et al., 2004; Soengas and Lowe, 2003).

PTEN expression as a melanoma therapeutic

Introduction of PTEN into advanced-stage melanoma cells via a chromosomal transfer or ectopic expression using a plasmid-based vector can inhibit tumor development in xenografted melanoma models by inducing cellular apoptosis (Poetsch et al., 2001b; Robertson et al., 1998a; Stahl et al., 2003). Furthermore, blocking PI3 kinase activity by expressing adenoviral based PTEN inhibited melanoma tumor development and reduced cellular invasiveness (Kotelevets et al., 2001; Stewart et al., 2002). Multiple groups have shown that PTEN expression can sensitize cancer cells to therapeutic agents that function by triggering apoptosis (Meier et al., 2005; Sinnberg et al., 2008; Stahl et al., 2003; Stewart et al., 2002; Wu et al., 2003). Thus, targeted delivery of PTEN into melanoma cells has potential to be an effective therapeutic agent. Furthermore, combining PTEN expression with other agents might help to prevent melanoma development completely. As multiple signaling cascades need to be inhibited for effective melanoma cell killing, targeted delivery vehicles, such as liposomes conjugated with specific antibodies to recognize melanoma cells, and loaded with pharmacological agents as well as PTEN expressing vectors might provide the tool for a therapeutic of this type. A case in point is breast cancer cell lines harboring a PTEN deletion or expressing a mutant functionally inactive PTEN protein, which exhibit extreme resistance to EGFR antagonists such as gefitinib (She et al., 2005). However, reconstitution of PTEN in these cell lines restored sensitivity to EGFR thereby inhibiting breast cancer xenograft development more effectively than either treatment alone (She et al., 2005). Similar observations are reported for NSCLC, prostate, and leukemia cell lines (She et al., 2005). Studies are warranted for melanoma, where low PTEN expression and/or activity lead to chemotherapeutic resistance. Restoration of functional PTEN in these cells would increase the therapeutic efficacy of anti-melanoma agents. Furthermore, if PTEN expression was regulated by endogenous microRNAs, inhibition using anti-miRs could significantly upregulate PTEN activity thereby restoring the chemosensitivity of the melanoma cells. However, PTEN regulation by microRNAs has not yet been reported in melanomas.

Therapeutic agents targeting Akt3

As targeting Akt3 alone or in combination inhibits melanoma growth by inducing apoptosis, several synthetic and naturally occurring small molecule inhibitors specifically inhibiting Akt activity have been developed and efficacy tested (Cheung et al., 2008; Madhunapantula et al., 2007; Robertson, 2005; Sharma et al., 2008, 2009; Soengas and Lowe, 2003; Stahl et al., 2004; Tran et al., 2008a). Recently, naturally occurring isothiocyanates were identified as agents with potential to reduce Akt3 activity in cancer cells including melanoma (Satyan et al., 2006; Sharma et al., 2008; Xiao and Singh, 2007). However, low potency of sulfur containing isothiocyanates would have required large doses to be consumed for clinical efficacy, which might have had side effects (Sharma et al., 2009). Therefore, Isoselenocyanates (ISCs) were created in which sulfur was replaced with selenium and the alkyl chain length was increased to make the compounds more cell-permeable (Figure 9A). Isoselenocyanates compounds with 4 (ISC-4) or 6 (ISC-6) carbon chains are effective at shrinking preexisting tumors by 60–70% (Figure 9B) by targeting Akt3 signaling (Figure 9C) thereby inducing apoptosis (Sharma et al., 2009). Compared with known inhibitors of Akt signaling such as API-2, the selenium containing ISC-4 and ISC-6 appear to be more effective for melanoma treatment (Sharma et al., 2009). BI-69A11 is another Akt inhibitor, demonstrated to have effective anti-melanoma activity in cultured cells and on tumors (Gaitonde et al., 2009). It is unknown whether side-effects associated with the use of these agents might also be a concern for treating melanoma, as Akt inhibition using siRNAs has been reported to induce the metastatic potential of breast cancer cells (Yoeli-Lerner et al., 2005).

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Figure 9.  ISC-4 inhibits melanoma tumor development by targeting Akt3 signaling. (A) Structures of 4 and 6 carbon containing isothiocyanates (phenylbutyl isothiocyanate (PBITC) and phenylhexyl isothiocyanate (PHITC)) and isoselenocyanates (ISC-4 and ISC6). (B) Isoselenocyanates (ISC-4 and ISC-6) were injected intra peritoneally into mice bearing established 50–60 mm3 sub-cutaneous melanoma tumors. Compared with DMSO vehicle controls or PBITC and PHITC, isoselenocyanates decreased tumor development by 60–70% (Sharma et al., 2009). (C) ISC-4 reduced Akt3 signaling in melanoma tumors. Decreased pAkt3 and downstream pPRAS40 were observed in tumors treated with ISC-4 indicating the compound decreased Akt3 signaling in tumors (Sharma et al., 2009).

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Targeting multiple pathways to synergistically treat melanoma

Small molecule inhibitors such as rapamycin, sorafenib, U0126, or PD98059 have been found to be ineffective as single agents for treating patients suffering from advanced melanoma (Lasithiotakis et al., 2008; Smalley and Herlyn, 2005). Furthermore, targeting oncogenic proteins singly seems not to be as effective as inhibiting multiple pathway for melanoma treatment (Lorigan et al., 2008; Smalley and Flaherty, 2009; Smalley et al., 2006). Simultaneously targeting PI3K/Akt3 and MAP kinase signaling pathways has been reported to synergistically inhibit melanoma development (Figure 10) (Cheung et al., 2008; Krasilnikov et al., 2003; Lopez-Bergami et al., 2008; Meier et al., 2005; Smalley and Flaherty, 2009; Tran et al., 2008a). First, delivering siRNAs inhibiting Akt3 and V600EB-Raf either by nucleofection or using liposomes synergistically inhibited melanoma tumor cells growth in culture or in xenografted melanoma tumors demonstrating the feasibility of this approach (Figure 10) (Cheung et al., 2008; Tran et al., 2008a). Second, combining nanoliposomes containing ceramide (a lipid based Akt inhibitor) with sorafenib (a Raf kinase inhibitor) has been shown to synergistically decrease melanoma cell growth (Tran et al., 2008b). Third, combined inhibition of MAPK (using sorafenib or mitogen-activated protein kinase kinase (MEK) inhibitors U0126, PD98059 and PD325901) and mTORC1 (using rapamycin) more effectively reduced melanoma cells growth compared with either of the agents tested singly (Dankort et al., 2009; Lasithiotakis et al., 2008; Lopiccolo et al., 2008; Luo, 2009). Fourth, topical application of LY-294002 and U0126 in combination more effectively delayed the development and decreased melanoma tumor incidence in the transgenic TPras mouse model when compared with either of these agents alone (Bedogni et al., 2006). Fifth, PI3K and MEK inhibitors only when used in combination were more effective than single agents (Lasithiotakis et al., 2008). Furthermore, targeting PI3K and mTOR activities using dual inhibitors NVP-BBD130 and NVP-BEZ235 had been shown to effectively reduce not only the size of primary melanoma tumor but also cervical lymphnode metastasis in a syngenic mouse melanoma model. These dual inhibitors exert anti-tumor activity by decreasing the activities of PI3K and mTORC1/mTORC2 complexes, causing a G1 phase cell cycle arrest by reducing cyclin D1 levels and increasing p27 protein expression (Marone et al., 2009). However, in no case did complete regression of melanoma tumors occur, which indicates that other targets or combinations will need to be identified and validated.

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Figure 10.  Targeting Akt3 and V600EB-Raf synergistically inhibits melanoma tumor development. SiRNAs targeting Akt3 (100 picomoles) and V600EB-Raf (12.5 picomoles) were introduced into UACC 903 melanoma cells alone or in combination, which were injected subcutaneously into mice and tumor development measured on alternate days up to days 17.5. Compared with controls (buffer, siScrambled or siC-Raf) an ∼60% reduction in tumor development was observed targeting Akt3 or V600EB-Raf alone. A much more dramatic reduction (∼80%) was observed when these proteins were targeted together. Inset shows decreased Akt3 and V600EB-Raf protein expression levels in melanoma tumors at days 9.5 (Cheung et al., 2008).

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It is fairly certain that both MAP and PI3 kinase pathways will need to be targeted as a part of a therapeutic cocktail to treat melanoma. Recently, hybrid compounds that inhibit these pathways have been developed and tested on cancer cell lines. One hybrid molecule is hexamethylene bisacetamide (HMBA), which simultaneously inhibits Akt and MAPK pathways and represses NFκB activity in breast cancer cell lines (Dey et al., 2008). Similarly, a selenium containing iNOS inhibitor, called PBISe, has been developed and its efficacy tested for inhibiting melanoma cell inhibition in vitro and in vivo (Madhunapantula et al., 2008). Intraperitoneally administered PBISe inhibits iNOS and PI3K/Akt3 signaling thereby inducing significant apoptosis in melanoma cells. Furthermore, PBISe-mediated inhibition of Akt3 signaling led to cell senescence by increasing pErk1/2 levels in melanoma cells. Unusually high MAPK activity induced cell senescence by elevating cdk inhibitors, such as p21, p16 and p27 (Michaloglou et al., 2005, 2008).

Inhibition of Akt3 expression or activity using siRNA or the pharmacological agent LY-294002 also has the potential to increase MAP kinase pathway activity in melanomas to levels that are inhibitory (Cheung et al., 2008). Mechanistically, this occurs because Akt3 phosphorylates V600EB-Raf on S364 and/or S428 to reduce its activity to levels that promote rather than inhibit melanoma development from melanocytes (Cheung et al., 2008) (Figure 7). Inhibiting Akt3 activity decreases this regulation leading to high, inhibitory levels of V600EB-Raf activity. In advanced melanomas, targeting these two proteins together using siRNA led to cooperative, synergistically acting tumor inhibition compared with targeting each protein singly (Figure 10). Although the above studies demonstrate the advantage of simultaneously targeting PI3 and MAP kinase pathways, complete tumor inhibition was not achieved again demonstrating the need to identify other proteins to target in combination with these. Therefore, multiple laboratories are working towards this goal by identifying key deregulated kinases promoting melanoma development to determine whether they inhibit melanoma growth synergistically when combined with targeting of Akt3 and V600EB-Raf.

Conclusions

  1. Top of page
  2. Summary
  3. Introduction
  4. PTEN and AKT3 in human melanomas
  5. Cellular processes regulated by PTEN/Akt3 signaling in melanomas
  6. Therapeutic potential of targeting the PTEN/Akt3 signaling cascade in melanomas
  7. Conclusions
  8. Key unanswered questions
  9. Acknowledgements
  10. References

In melanomas, PTEN loss and activation of Akt3 occur frequently. While mechanisms leading to Akt3 activation in melanomas are not fully characterized, it is known that overexpression of Akt3 and decreased PTEN activity play important roles in this process. Expression of PTEN or targeted reduction of Akt3 activity has also been shown to reduce the survival of melanoma tumor cells leading to inhibition of tumor development and sensitization of melanoma cells to apoptosis-inducing agents. Therefore, expression of PTEN or targeting Akt3 directly or by interfering with upstream proteins regulating these genes, promises a new and more effective therapeutic approach for melanoma treatment.

Key unanswered questions

  1. Top of page
  2. Summary
  3. Introduction
  4. PTEN and AKT3 in human melanomas
  5. Cellular processes regulated by PTEN/Akt3 signaling in melanomas
  6. Therapeutic potential of targeting the PTEN/Akt3 signaling cascade in melanomas
  7. Conclusions
  8. Key unanswered questions
  9. Acknowledgements
  10. References

By promoting cell survival and proliferation, the PTEN and Akt3 signaling cascade plays an important role in melanomas. Nevertheless, an expanding number of major questions remain to be answered. For example, what is the mechanism of selective Akt3 activation in melanomas? Would therapeutically targeting Akt3 in human patients effectively inhibit melanoma development? If combination therapies are required, what other kinases would synergize with Akt3 in melanomas? Will targeting Akt3 promote melanoma metastasis? Which Akt3 substrate needs to be targeted for effective melanoma tumor inhibition? Do microRNAs regulate PTEN expression in melanomas? Does phosphorylation of PTEN affect melanoma development? Addressing these aspects might provide better understanding of melanoma development and thereby aid in the generation of novel therapeutics.

Acknowledgements

  1. Top of page
  2. Summary
  3. Introduction
  4. PTEN and AKT3 in human melanomas
  5. Cellular processes regulated by PTEN/Akt3 signaling in melanomas
  6. Therapeutic potential of targeting the PTEN/Akt3 signaling cascade in melanomas
  7. Conclusions
  8. Key unanswered questions
  9. Acknowledgements
  10. References

The Foreman Foundation for Melanoma Research, American Cancer Society and NIH-RO1 (CA-127892-01A), NIH-RO3 (CA-119309) are gratefully acknowledged for support of this work.

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  2. Summary
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  4. PTEN and AKT3 in human melanomas
  5. Cellular processes regulated by PTEN/Akt3 signaling in melanomas
  6. Therapeutic potential of targeting the PTEN/Akt3 signaling cascade in melanomas
  7. Conclusions
  8. Key unanswered questions
  9. Acknowledgements
  10. References
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