The STAT3 oncogene as a predictive marker of drug resistance

被引:104
作者
Barre, Benjamin
Vigneron, Arnaud
Perkins, Neil
Roninson, Igor B.
Gamelin, Erick
Coqueret, Olivier [1 ]
机构
[1] INSERM, U564, Canc Ctr Paul Papin, F-49033 Angers, France
[2] Sch Life Sci, Div Gene Regulat & Express, Dundee DD1 5EH, Scotland
[3] Ordway Res Inst, Ctr Canc, Albany, NY 12208 USA
关键词
D O I
10.1016/j.molmed.2006.11.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Constitutive activation of STAT3 (signal transducer and activator of transcription) has been reported in several primary cancers and tumor cell lines where it induces cell transformation through a combined inhibition of apoptosis and cell-cycle activation. Several studies have suggested that STAT3 prevents cell-cycle arrest and cell death through upregulation of survival proteins and downregulation of tumor suppressors. As a consequence of anti-apoptotic and proliferative lesions, we propose that this oncogenic pathway is also involved in intrinsic drug resistance and that STAT3-expressing tumors are resistant to chemotherapeutic agents. If this hypothesis is correct, the detection of the activated form of this protein should help to define subsets of tumors that fail to respond to chemotherapy. Furthermore, interfering with the STAT3 oncogenic pathway might restore the sensitivity to anticancer drugs.
引用
收藏
页码:4 / 11
页数:8
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