The Dark Side of E2F1: In Transit beyond Apoptosis

被引:129
作者
Engelmann, David [1 ]
Puetzer, Brigitte M. [1 ]
机构
[1] Univ Rostock, Dept Vectorol & Expt Gene Therapy, Biomed Res Ctr, D-18057 Rostock, Germany
关键词
CELL-PROLIFERATION; MUTANT P53; PROGRESSION; MELANOMA; RECEPTOR; METASTASIS; DETERMINES; ACTIVATION; MIGRATION; INVASION;
D O I
10.1158/0008-5472.CAN-11-2575
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
E2F1 plays a critical role in cell-cycle progression and the induction of apoptosis in response to DNA damage. The latest evidence has uncovered that this tumor suppressor is most relevant for cancer progression and chemoresistance. Increased abundance of E2F1 triggers invasion and metastasis by activating growth receptor signaling pathways, which in turn promote an antiapoptotic tumor environment. The data shed light on the molecular mechanisms underlying E2F1-induced prometastatic activity and predict its radical switch from a mediator of cell death toward an accelerator of tumor progression. This raises the perspective of new drug targets at late-stage cancer. Cancer Res; 72(3); 571-5. (C) 2012 AACR.
引用
收藏
页码:571 / 575
页数:5
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