Wanitchakool Podchanart, Wolf Luisa, Koehl Gudrun E, Sirianant Lalida, Schreiber Rainer, Kulkarni Sucheta, Duvvuri Umamaheswar, Kunzelmann Karl
Institut für Physiologie, Universität Regensburg, , Universitätsstraße 31, Regensburg 93053, Germany.
Philos Trans R Soc Lond B Biol Sci. 2014 Feb 3;369(1638):20130096. doi: 10.1098/rstb.2013.0096. Print 2014 Mar 19.
Anoctamin 1 (TMEM16A, Ano1) is a recently identified Ca(2+)-activated chloride channel and a member of a large protein family comprising 10 paralogues. Before Ano1 was identified as a chloride channel protein, it was known as the cancer marker DOG1. DOG1/Ano1 is expressed in gastrointestinal stromal tumours (GIST) and particularly in head and neck squamous cell carcinoma, at very high levels never detected in other tissues. It is now emerging that Ano1 is part of the 11q13 locus, amplified in several types of tumour, where it is thought to augment cell proliferation, cell migration and metastasis. Notably, Ano1 is upregulated through histone deacetylase (HDAC), corresponding to the known role of HDAC in HNSCC. As Ano1 does not enhance proliferation in every cell type, its function is perhaps modulated by cell-specific factors, or by the abundance of other anoctamins. Thus Ano6, by regulating Ca(2+)-induced membrane phospholipid scrambling and annexin V binding, supports cellular apoptosis rather than proliferation. Current findings implicate other cellular functions of anoctamins, apart from their role as Ca(2+)-activated Cl(-) channels.
anoctamin 1(TMEM16A,Ano1)是一种最近被鉴定出的钙激活氯离子通道,是一个由10个旁系同源物组成的大蛋白质家族的成员。在Ano1被鉴定为氯离子通道蛋白之前,它被称为癌症标志物DOG1。DOG1/Ano1在胃肠道间质瘤(GIST)中表达,特别是在头颈部鳞状细胞癌中,其表达水平非常高,在其他组织中从未检测到。现在发现Ano1是11q13基因座的一部分,在几种肿瘤类型中发生扩增,据认为它在这些肿瘤中可促进细胞增殖、细胞迁移和转移。值得注意的是,Ano1通过组蛋白去乙酰化酶(HDAC)上调,这与HDAC在头颈部鳞状细胞癌中的已知作用相对应。由于Ano1并非在每种细胞类型中都能增强增殖,其功能可能受到细胞特异性因子或其他anoctamins丰度的调节。因此,Ano6通过调节钙诱导的膜磷脂紊乱和膜联蛋白V结合,支持细胞凋亡而非增殖。目前的研究结果表明,anoctamins除了作为钙激活氯离子通道的作用外,还具有其他细胞功能。