Van Laethem An, Garmyn Marjan, Agostinis Patrizia
Department of Molecular and Cell Biology, Cell Death Research and Therapy Laboratory, Catholic University of Leuven, Campus Gasthuisberg, Herestraat 49, B-3000, Belgium.
Photochem Photobiol Sci. 2009 Mar;8(3):299-308. doi: 10.1039/b813346h. Epub 2009 Jan 5.
The ultraviolet (UV) B portion of the UV light has been recognized as the most prominent risk factor for the development of skin cancer, the most common malignancy in the Caucasian population. At the cellular level, UVB signal transduction regulates replicative arrest and DNA repair, gene expression and, when damage is beyond repair, apoptotic cell death, which is induced to protect the host against the accumulation of potentially mutagenic keratinocytes. An increasing body of evidence indicates that the UVB response in skin is a complex and multifaceted biological process. The UVB signal transduction originates at multiple intracellular sites, and the cross talk between dedicated molecular mediators acting within a complex signal network, determines whether the UVB damaged cell will survive, proliferate or die. However, very little is known about the original targets or direct chromophores that put in motion the UVB response in its main target: the keratinocyte. In this review we discuss the recent identification of signalling pathways linking apical UVB mediated damaging events with the induction of apoptosis. Understanding the molecular mechanisms that underlie the process of apoptotic cell death in UVB exposed keratinocytes, is of outmost importance to reveal how defects in apoptotic pathways can contribute to skin cancer.
紫外线(UV)中的UVB部分已被公认为是皮肤癌发生的最主要风险因素,皮肤癌是白种人最常见的恶性肿瘤。在细胞水平上,UVB信号转导调节复制停滞和DNA修复、基因表达,并且当损伤无法修复时,诱导凋亡性细胞死亡,以保护宿主免受潜在诱变角质形成细胞的积累。越来越多的证据表明,皮肤中的UVB反应是一个复杂且多方面的生物学过程。UVB信号转导起源于多个细胞内位点,在复杂信号网络中起作用的特定分子介质之间的相互作用,决定了UVB损伤的细胞是存活、增殖还是死亡。然而,对于引发UVB反应的主要靶细胞——角质形成细胞中的原始靶点或直接发色团,我们却知之甚少。在这篇综述中,我们讨论了将顶端UVB介导的损伤事件与凋亡诱导联系起来的信号通路的最新研究发现。了解UVB照射的角质形成细胞中凋亡性细胞死亡过程的分子机制,对于揭示凋亡途径缺陷如何导致皮肤癌至关重要。