Literature DB >> 18930345

Down-regulation of stathmin is required for TGF-beta inducible early gene 1 induced growth inhibition of pancreatic cancer cells.

Lei Jiang1, Yangchao Chen, Chu-yan Chan, Xin Wang, Lin Lin, Ming-liang He, Marie C M Lin, David T Yew, Joseph J Y Sung, Ji-Cheng Li, Hsiang-fu Kung.   

Abstract

Transforming growth factor-beta (TGF-beta) inducible early gene 1 (TIEG1) is known to induce apoptosis in TGF-beta sensitive pancreatic cancer cells, yet its effect on TGF-beta resistant cancer cells remains unclear. In this study, TIEG1 was found to induce apoptosis in TGF-beta resistant cancer cells and concurrently enhanced gemcitabine chemosensitivity. Down-regulation of stathmin was noted to associate with TIEG1 expression, whilst ectopic overexpression of stathmin prevented TIEG1 mediated growth inhibition of tumor cells. Small interfering RNAs targeting stathmin inhibited pancreatic cancer cell growth. These suggest that stathmin is a downstream target of TIEG1.

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Year:  2008        PMID： 18930345     DOI： 10.1016/j.canlet.2008.09.017

Source DB:  PubMed          Journal:  Cancer Lett        ISSN： 0304-3835            Impact factor:   8.679


  16 in total

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