Department of Molecular Biology of Cancer, Medical University of Lodz, Lodz, Poland.
Department of Molecular Biology of Cancer, Medical University of Lodz, Lodz, Poland.
J Invest Dermatol. 2015 Feb;135(2):352-358. doi: 10.1038/jid.2014.319. Epub 2014 Aug 21.
Melanoma is a therapy-resistant skin cancer due to numerous mechanisms supporting cell survival. Although components of melanoma cytoprotective mechanisms are overexpressed in many types of tumors, some of their regulators are characteristic for melanoma. Several genes mediating pro-survival functions have been identified as direct targets of microphthalmia-associated transcription factor (MITF), a melanocyte-specific modulator also recognized as a lineage addiction oncogene in melanoma. BRAF(V600E) and other proteins deregulated in melanoma influence MITF expression and activity, or they are the partners of MITF in melanoma response to radiotherapy and chemotherapeutics. In this review, the pro-survival activity of MITF is discussed.
黑色素瘤是一种对治疗有抵抗力的皮肤癌,这是由于有许多支持细胞存活的机制。虽然黑色素瘤细胞保护机制的成分在许多类型的肿瘤中过度表达,但其中一些调节剂是黑色素瘤所特有的。已经鉴定出几种介导存活功能的基因作为小眼畸形相关转录因子 (MITF) 的直接靶标,MITF 是一种黑素细胞特异性调节剂,也被认为是黑色素瘤中的谱系成瘾癌基因。黑色素瘤中失调的 BRAF(V600E) 和其他蛋白质会影响 MITF 的表达和活性,或者它们是 MITF 在黑色素瘤对放疗和化疗反应中的伙伴。在这篇综述中,讨论了 MITF 的促存活活性。