Vasioukhin Valeri
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Dev Neurosci. 2006;28(1-2):13-24. doi: 10.1159/000090749.
Cell polarity is one of the most basic properties of all normal cells and loss of polarity is a hallmark of cancer. While multiple proteins have been implicated in the maintenance of cell polarity, the functionally related neoplastic tumor suppressors Lethal giant larvae (Lgl), Scribble and Disks large comprise a unique group of molecules that are not only involved in the maintenance of cell polarity, but also in the regulation of cell proliferation and cancer. Lgl is the first identified member of this group. Loss of Lgl leads to massive tissue disorganization, tumor-like growth and lethal phenotypes in both Drosophila and mice. Lgl mutant cells display disruption of cell polarity, failure of asymmetric cell division, deregulation of Notch signaling and loss of proper cell fate determination. Lgl is a critical downstream target of the Par6/aPKC cell polarity complex; however, the functional role of Lgl itself and, specifically, the mechanisms of Lgl function in cell polarity and regulation of cell proliferation remain enigmatic. This minireview summarizes available information and discusses potential mechanisms of Lgl function.
细胞极性是所有正常细胞最基本的特性之一,而极性丧失是癌症的一个标志。虽然多种蛋白质与细胞极性的维持有关,但功能相关的肿瘤抑制因子致死巨幼虫(Lgl)、scribble和盘状大蛋白构成了一组独特的分子,它们不仅参与细胞极性的维持,还参与细胞增殖和癌症的调控。Lgl是该组中第一个被鉴定的成员。Lgl的缺失会导致果蝇和小鼠出现大量组织紊乱、肿瘤样生长和致死表型。Lgl突变细胞表现出细胞极性破坏、不对称细胞分裂失败、Notch信号失调以及细胞命运决定异常。Lgl是Par6/aPKC细胞极性复合体的关键下游靶点;然而,Lgl本身的功能作用,特别是Lgl在细胞极性和细胞增殖调控中的作用机制仍然不明。本综述总结了现有信息,并讨论了Lgl功能的潜在机制。