Bypassing melanocyte senescence by β-catenin: A novel way to promote melanoma

被引:17
作者
Larue, L. [1 ,2 ]
Luciani, F. [1 ,2 ]
Kumasaka, M. [1 ,2 ]
Champeval, D. [1 ,2 ]
Demirkan, N. [1 ,2 ,3 ]
Bonaventure, J. [1 ,2 ]
Delmas, V. [1 ,2 ]
机构
[1] Inst Curie, F-91405 Orsay, France
[2] CNRS, UMR Curie 146, F-91405 Orsay, France
[3] Pamukkale Univ, Tp Fak, Patol Anabilim Dal, Knkl Denizli, Turkey
来源
PATHOLOGIE BIOLOGIE | 2009年 / 57卷 / 7-8期
关键词
Catenin; Senescence; Melanoma; CELLULAR SENESCENCE; MALIGNANT-MELANOMA; CUTANEOUS MELANOMA; TUMOR SUPPRESSION; NEURAL CREST; EXPRESSION; GENE; IMMORTALIZATION; MUTATIONS; DIFFERENTIATION;
D O I
10.1016/j.patbio.2008.11.003
中图分类号
R36 [病理学];
学科分类号
100103 [病原生物学];
摘要
The Wnt/beta-catenin signaling pathway plays a key role in several cellular functions during embryonic development and adult homeostasis. The deregulation of this pathway may lead to the development of cancer, including melanoma. Deregulation of the Wnt/beta-catenin pathway occurs through either the induction/repression of, or specific mutations in, various members of this signaling pathway; this results in the stabilization of beta-catenin and its translocation from the cytoplasm to the nucleus, where it regulates transcription. Although nuclear beta-catenin is clearly involved in malignant transformation, the mechanism by which it exerts its effects remains elusive. This review focuses on the molecular and cellular mechanisms that are driven by beta-catenin and lead to melanocyte transformation. In particular, we describe how beta-catenin induces melanocyte immortalization, a novel activity of this multifunction protein. Finally, we discuss how beta-catenin-induced immortalization can cooperate with MAPKinase pathways to produce melanoma. (C) 2008 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:543 / 547
页数:5
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