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揭示缺氧诱导因子-1α在皮肤癌发生中的作用。

Uncovering the role of hypoxia inducible factor-1α in skin carcinogenesis.

作者信息

Nys Kris, Maes Hannelore, Dudek Aleksandra Maria, Agostinis Patrizia

机构信息

Cell Death Research & Therapy Laboratory, Department Molecular and Cell Biology, Faculty of Medicine, Catholic University of Leuven, Herestroat 49, box 901, B-3000, Belgium.

出版信息

Biochim Biophys Acta. 2011 Aug;1816(1):1-12. doi: 10.1016/j.bbcan.2011.02.001. Epub 2011 Feb 19.

DOI:10.1016/j.bbcan.2011.02.001
PMID:21338656
Abstract

The hypoxia inducible factor-1α (HIF-1α) is a pleiotropic transcription factor typically activated in response to low oxygen tension as well as other stress factors in normoxic conditions. Upon activation HIF-1α mediates the transcriptional activation of target genes involved in a variety of processes comprising stress adaptation, metabolism, growth and invasion, but also apoptotic cell death. The molecular mechanisms, signaling pathways and downstream targets evoked by the activation of HIF-1α in epidermal cells are becoming increasingly understood and underscore the participation of HIF-1α in crucial processes including malignant transformation and cancer progression. Recent studies have implicated HIF-1α as an integral part of the multifaceted signal transduction initiated by the exposure of keratinocytes to ultraviolet radiation B (UVB), which represents the most ubiquitous hazard for human skin and the principal risk factor for skin cancer. HIF-1α activation by UVB exposure contributes to either repair or the removal of UVB-damaged keratinocytes by inducing apoptosis, thus revealing a tumor suppressor role for HIF-1α in these cells. On the other hand, the constitutive expression of HIF-1α evoked by the mild hypoxic state of the skin has been implicated as a positive factor in the transformation of normal melanocytes into malignant melanoma, one of the most aggressive types of human cancers. Here we review the uncovered and complex role of HIF-1α in skin carcinogenesis.

摘要

缺氧诱导因子-1α(HIF-1α)是一种多效性转录因子,通常在低氧张力以及常氧条件下的其他应激因素作用下被激活。激活后,HIF-1α介导参与多种过程的靶基因的转录激活,这些过程包括应激适应、代谢、生长和侵袭,也包括凋亡性细胞死亡。表皮细胞中HIF-1α激活所引发的分子机制、信号通路和下游靶点越来越为人所知,并突出了HIF-1α在包括恶性转化和癌症进展在内的关键过程中的参与。最近的研究表明,HIF-1α是角质形成细胞暴露于紫外线B(UVB)引发的多方面信号转导的一个组成部分,UVB是对人类皮肤最普遍的危害,也是皮肤癌的主要危险因素。UVB暴露激活HIF-1α通过诱导凋亡有助于修复或清除UVB损伤的角质形成细胞,从而揭示了HIF-1α在这些细胞中的肿瘤抑制作用。另一方面,皮肤轻度缺氧状态引起的HIF-1α组成性表达被认为是正常黑素细胞转化为恶性黑色素瘤(人类最具侵袭性的癌症类型之一)的一个积极因素。在此,我们综述了HIF-1α在皮肤癌发生中尚未被发现的复杂作用。

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