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UL16-binding protein 2 (ULBP2) is one of the ligands for NKG2D (NKG2DL). ULBP2 expression is induced in transformed cells and is recognized by immune effector cells via the activating NKG2D immunoreceptor. Soluble forms of NKG2DL have been reported in the serum of patients with several types of cancer. The present study investigated the diagnostic and prognostic significance of serum-soluble ULBP2 (sULBP2) in lung cancer patients. We used flow cytometry to evaluate the surface expression of NKG2DL by various lung cancer cells, while sULBP2 was measured using our original ELISA. In addition, the immunological effect of sULBP2 on peripheral blood mononuclear cells (PBMC) was examined by the 51Cr release assay. We found that ULBP2 was highly expressed and that the sULBP2 level was elevated in supernatants of cultured non-small-cell lung cancer (NSCLC) cells as well as in the serum of NSCLC patients. ULBP2 levels were especially high in squamous cell carcinoma (SQ) patients. Clinical stage IIIB and IV NSCLC patients with a sULBP2 level ≥8.7 pg/mL showed significantly shorter survival than patients with sULBP2 <8.7 pg/mL. In multivariate analysis, a sULBP2 level ≥8.7 pg/mL (hazard ratio [HR], 2.13; P = 0.038) and clinical stage IV (HR, 2.65; P = 0.019) were independent determinants of a poor outcome. As a possible mechanism, we demonstrated that sULBP2 directly suppresses the cytolytic activity of PBMC. In conclusion, ULBP2 is the most significant NKG2DL for lung cancer, and sULBP2 is useful in the diagnosis of SQ and as a prognostic indicator for patients with advanced NSCLC. (Cancer Sci, doi: 10.1111/j.1349-7006.2012.02330.x, 2012)
Lung cancer is the leading cause of cancer death around the world. Despite the recent development of multidisciplinary therapy, the prognosis for lung cancer patients is still very poor, largely due to the advanced stage of their tumors at the time of diagnosis and the unpredictable behavior of the disease. Therefore, effective detection of lung cancer and provision of suitable therapy depending on each patient's prognosis using biomarkers are of vital importance.
The host immune response to tumor cells is mediated by innate and adaptive immune processes that involve lymphocytes such as natural killer (NK) cells, CD8 T cells and γδ+ T cells. These cells have also been reported to play an important role in host immunity against lung cancer. Various studies have revealed the mechanisms used by these effector cells to recognize and attack tumor cells. NKG2D is an activating receptor that is expressed by NK cells, CD8+ αβ+ T cells, γδ+ T cells and NKT cells. The ligands for NKG2D are generally not expressed by normal cells, but their expression is induced in infected or transformed cells that should be eliminated by the host immune system. NKG2D recognizes its ligands expressed on the surface of target cells and then augments the cytolytic activity and cytokine production of effector cells. Therefore, the NKG2D–NKG2D ligand system is thought to play an essential role in host tumor immunity.
A diverse range of ligands for NKG2D has recently been identified. In humans they consist of two families with structural similarities. One is the MHC class I chain-related (MIC) family of molecules (MICA and MICB), and the other is a family of cell surface glycoproteins that can bind to human cytomegalovirus UL16 proteins (the ULBP family: ULBP1-4, RAET1G and RAET1L).[8-12] In vivo expression of NKG2D ligands is very limited in normal tissues,[13, 14] whereas the constitutive expression of NKG2D ligands has been reported in many malignant tumors, and such expression is correlated with the NKG2D-dependent cytotoxicity[15-18] of immune effector cells. Therefore, NKG2D ligands might be a possible marker of transformed cells that have the potential to modify host immune responses.
Recently, it was demonstrated that NKG2D ligands are released in soluble form from the surface of cancer cells,[19-21] and that soluble ligands can be measured in the serum of cancer patients. Indeed, elevated serum levels of soluble MICA,[19, 22-32] MICB[20, 25, 29, 32] and ULBP2[21, 27] have been detected in cancer patients. In addition, several clinical studies have suggested a correlation between the level of soluble MICA (sMICA) and a poor prognosis.[23, 33] Therefore, soluble NKG2D ligands might have several useful properties as diagnostic/prognostic markers for cancer.
In the present study, we evaluated the pattern of expression of NKG2D ligands by a panel of lung cancer cell lines and focused on the soluble form of ULBP2 in the serum of lung cancer patients, and investigated its usefulness as a diagnostic and prognostic marker for lung cancer.
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- Materials and Methods
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- Supporting Information
In the present study, we found that cell surface ULBP2 is the NKG2D ligand most widely and strongly expressed by lung cancer cells, and that sULBP2 increased in lung cancer cell line culture supernatants in proportion to the level of cell surface expression of ULBP2, especially with NSCLC cells. Also, serum sULBP2 was detectable in lung cancer patients. The diagnostic performance of sULBP2 was substantially superior for NSCLC, and was comparable to the well-known tumor marker SCC-Ag for the diagnosis of SQ patients. Finally, we demonstrated that sULBP2 is an excellent prognostic indicator for NSCLC. As a possible explanation, we showed that sULBP2 directly suppresses the activity of immune effector cells. These findings indicate that sULBP2 is a promising diagnostic and prognostic marker for NSCLC.
In the present study, we observed that ULBP2 was the NKG2D ligand most frequently and strongly expressed by lung cancer cells. However, the only other study on the pattern of NKG2D ligand expression by lung cancer cells yielded different results. Le Maux Chansac et al. studied 12 human NSCLC cell lines and reported that MICA or MICB and ULBP3 were expressed by most cell lines, while ULBP1 and ULBP2 were rarely expressed. We suspect that the low expression of ULBP2 in their study might have been related to the fixation methods used before examination using flow cytometry. In their study, cells were fixed with formaldehyde before analysis, but it has been suggested that fixation of membrane lipids by formaldehyde is unreliable. Our observations are supported by a study on the expression of NKG2D ligands by normal human bronchial epithelial (NHBE) cells. Borchers et al. reported that ULBP2 mRNA was constitutively expressed at the highest level among NKG2D ligands by NHBE cells from four separate donors. They also reported that surface expression of ULBP2 was clearly increased after hydrogen peroxide treatment of these cells. Their data suggest that bronchial cells might show increased ULBP2 expression after exposure to stress, and might support our observations that ULBP2 is most broadly expressed by transformed cells originating in the lungs. Therefore, we believe that ULBP2 might be most abundantly expressed among NKG2D ligands in lung cancer and play a pivotal role in tumor immunity.
Although reports describing the clinical significance of soluble NKG2D ligands in the serum of cancer patients have been increasing recently, information about lung cancer is still rare. The soluble form of MICA was reported to be elevated in the serum of patients with leukemia, multiple myeloma, prostate cancer, ovarian cancer, osteosarcoma, melanoma, gastrointestinal tumors, neuroblastoma, pancreatic cancer, cervical cancer and hepatocellular carcinoma.[31, 32] Elevation of soluble MICB (sMICB) has also been reported in patients with ovarian cancer, gastrointestinal malignancies, pancreatic cancer and hepatocellular carcinoma. Regarding lung cancer, to our knowledge, only one such study has been reported by Holdenrieder et al. They measured sMICA and sMICB in 19 lung cancer patients, and reported elevation of both MICA and MICB. However, detailed clinical information on their lung cancer patients was not provided. These observations suggest the possible usefulness of soluble NKG2D ligands as serum markers for various cancers, and the current lack of data about lung cancer suggests that it should be more thoroughly studied.
Compared with studies about soluble MIC family ligands, studies on serum sULBP2 in cancer patients are uncommon and the results are controversial. Waldhauer et al. first reported elevated serum levels of sULBP2 in patients with hematopoietic malignancies, but they could not find sULBP2 in patients with gastrointestinal malignancies. Li et al. studied eight ovarian cancer patients and reported that serum sULBP2 was not detectable. After failing to detect sULBP2 in the serum of patients with solid tumors, Paschen et al. recently found elevated serum levels of sULBP2 in melanoma patients. There are several possible explanations for the discrepancies among these reports. First, the presence of soluble NKG2D ligands is possibly dependent on tumor histology and such ligands might be detectable in a more limited range of solid malignancies compared with hematopoietic malignancies. Second, the sensitivity of the ELISA used in each study would have a significant influence on the detectability of sULBP2. Waldhauer et al. used an ELISA that detected sULBP2 at levels as low as 20 pg/mL, but the detection limit was not described for the ELISA in the other two studies. We established an original ELISA that could detect sULBP2 at a concentration of 7.8 pg/mL (Fig. S1). Further studies are needed to clarify whether sULBP2 can be detected in the serum of patients with various solid cancers after the sensitivity of the assay has been thoroughly quantified.
In the present study, we also showed that sULBP2 was a significant prognostic marker for NSCLC. Several previous studies have shown a correlation between elevated levels of sMICA and a poor prognosis for patients with multiple myeloma and oral squamous cell carcinoma. Regarding sULBP2, the former report for melanoma patients is consistent with the present study, which found elevated levels of sULBP2 were correlated with a poor prognosis. However, the reason for this correlation is not discussed in their report and remains unknown because of the lack of information regarding the function of sULBP2. Although multiple studies have shown an inhibitory effect of sMICA on host effector cell function,[28, 29, 39] to our knowledge, only one study has addressed this issue for sULBP proteins. In that study, a possible inhibitory effect of sULBP proteins was indirectly suggested by the decreased surface expression of NKG2D in NK cells incubated with the culture supernatants of gastric cancer cells expressing ULBP1-3 protein. Therefore, the role of sULBP1-3 protein has not been demonstrated separately and the function of sULBP2 remains unknown. In the present study, we clearly showed that sULBP2 itself suppresses the cytotoxic activity of host effector cells. This finding might help us to understand the mechanism leading to deterioration of the prognosis in patients with high serum levels of sULBP2.
There are several possible mechanisms by which sULBP2 suppress the activities of immune effector cells. First, soluble NKG2D ligands might downregulate the surface expression of NKG2D on the effector cells. This mechanism has been proposed in the case of sMICA in several reports.[22, 31, 39] Second, soluble NKG2D ligands might competitively bind to NKG2D on the effector cells, and thereby inhibit the binding of the cell surface NKG2D ligands to this receptor and the following activation of the effector cells. Last, soluble NKG2D ligands might activate immunosuppressive T cells, thereby inhibiting effector cell function of PBMC. For example, several studies have reported that sMICA can activate NKG2D+CD4+ T cells that possess immunosuppressive function.[41, 42] Compared with these mechanistic studies of sMICA, little is known about sULBP2. Therefore, further study of this mechanism is needed to overcome the immunosuppressive effect of sULBP2.
It is noteworthy that there was a discrepancy between the level of cell surface expression of ULBP2 and the level of sULBP2 in SCLC cell line supernatants in the present study, while a clear correlation was seen for NSCLC cell lines. This discrepancy might have been caused by loss of the shedding mechanism for ULBP2 in this type of cancer. Recently, several mechanisms have been proposed for the shedding of NKG2D ligands from the cell surface. These involve metalloproteinases and ERp5 for MICA, phosphatidylinositol-specific phospholipase C for GPI-anchored ULBP proteins, a disintegrin and metalloproteinase family proteases for ULBP2,[21, 44] and release as part of membrane vesicles for ULBP3. Although it is still unknown whether one or more of these mechanisms operates for ULBP2 in lung cancer, some might be inhibited in SCLC cells. Another possibility is that the shedding-resistant form of ULBP2 might be expressed in SCLC cells by genomic mutation or alternative splicing. In any case, understanding the mechanism of both shedding seen in NSCLC and its inhibition in SCLC could be important, because it might help us to manipulate this process in order to modify host antitumor immunity.
Unlike the results of an undetectable level of sULBP2 in the culture supernatant of SCLC cell lines in vitro, the serum level of sULBP2 was significantly elevated in SCLC patients. Although the exact reason for this discrepancy is unclear, the same discrepancies were reported previously in other tumor markers. For example, CYFRA 21-1, a potential tumor marker for NSCLC, is rarely detectable in the supernatant of cultured SCLC cells, whereas it is elevated in nearly half of the sera of SCLC patients.[46, 47] One possible mechanism for these discrepancies is the excessive leakage from cancer cells or from involved normal tissues by coexisting inflammation of the cancerous lesion. Another possibility is secretion from the concomitant NSCLC component in the histological heterogenous SCLC lesion, known as combined SCLC. In any case, we believe that the clinical significance of serum sULBP2 in SCLC patients is limited, because the level of elevation is very low compared with those seen in NSCLC patients.
In conclusion, we detected sULBP2 in the serum of lung cancer patients and found that it was useful in the diagnosis of NSCLC, especially SQ. In addition, sULBP2 was an independent prognostic indicator for advanced NSCLC. We also observed that sULBP2 has significantly inhibited the cytolytic activity of host effector cells. These findings indicate that sULBP2 is a useful diagnostic and prognostic marker for lung cancer patients. In addition, further study on the shedding process of sULBP2 might be useful for modulating the immune response in cancer patients.