Journal of Cellular Biochemistry

Rottlerin inhibits migration of follicular thyroid carcinoma cells by PKCδ-independent destabilization of the focal adhesion complex

Authors

  • Chien-Jung Lin,

    1. Department of Anatomy and Cell Biology, College of Medicine, National Taiwan University, 1-1 Jen-Ai Road, Taipei 10051, Taiwan
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  • Chieh-Yu Lin,

    1. Department of Anatomy and Cell Biology, College of Medicine, National Taiwan University, 1-1 Jen-Ai Road, Taipei 10051, Taiwan
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  • Ying Chen,

    1. Department of Anatomy and Cell Biology, College of Medicine, National Taiwan University, 1-1 Jen-Ai Road, Taipei 10051, Taiwan
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  • Shih-Horng Huang,

    Corresponding author
    1. Division of General Surgery, Department of Surgery, Far Eastern Memorial Hospital, Taipei 220, Taiwan
    2. Yuan Ze University Graduate School of Biotechnology and Bioengineering, Taoyuan, Taiwan
    • Department of Surgery and Division of General Surgery, Far Eastern Memorial Hospital, Taipei 220, Taiwan; Yuan Ze University Graduate School of Biotechnology and Bioengineering, Taoyuan, Taiwan.
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  • Seu-Mei Wang

    Corresponding author
    1. Department of Anatomy and Cell Biology, College of Medicine, National Taiwan University, 1-1 Jen-Ai Road, Taipei 10051, Taiwan
    • Department of Anatomy and Cell Biology, College of Medicine, National Taiwan University, 1-1 Jen-Ai Road, Taipei, Taiwan 10051, Taiwan.
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  • Part of this work was presented at the 10th European Congress of Endocrinology, Berlin, Germany (May 3–7, 2008).

  • Chien-Jung Lin and Chieh-Yu Lin contributed equally to this study.

Abstract

This study examined the effect of rottlerin on the focal adhesion-mediated cell migration of CGTH W-2 human follicular thyroid carcinoma cells. Rottlerin (10 µM) resulted in decreased adhesion of CGTH W-2 cells to matrix substance, which was correlated with metastatic potential. Rottlerin treatment also resulted in a marked reduction in the migration of CGTH W-2 cells. Protein levels of integrin β1, FAK, and paxillin were decreased by rottlerin. Consistent with this, immunostaining of FAK, vinculin, and paxillin revealed disassembly of the focal adhesions. Disruption of actin stress fibers was noted, which was compatible with reduced expression levels and activities of Rac-1 and Rho. The effect of rottlerin on cell migration was not attributable to inhibition of PKCδ activity since siRNA knockdown of PKCδ did not recapitulate the effects of rottlerin on cell adhesion and migration. Furthermore, activation of PKCδ by phorbol esters failed to restore the rottlerin-inhibited migratory ability. The mitochondrial uncoupler, carbonylcyanide-4-(trifluoromethoxy)-phenylhydrazone, was able to mimic several rottlerin's effects. In summary, we demonstrated that rottlerin inhibits the migration of CGTH W-2 cells by disassembly of focal adhesion complexes in a PKCδ-independent manner, and might play as a mitochondrial uncoupler role in these events. J. Cell. Biochem. 110: 428–437, 2010. © 2010 Wiley-Liss, Inc.

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