Humbert P O, Grzeschik N A, Brumby A M, Galea R, Elsum I, Richardson H E
Cell Cycle and Cancer Genetics Laboratory, Research Division, Peter MacCallum Cancer Center, Melbourne, Victoria, Australia.
Oncogene. 2008 Nov 24;27(55):6888-907. doi: 10.1038/onc.2008.341.
The neoplastic tumour suppressors, Scribble, Dlg and Lgl, originally discovered in the vinegar fly Drosophila melanogaster, are currently being actively studied for their potential role in mammalian tumourigenesis. In Drosophila, these tumour suppressors function in a common genetic pathway to regulate apicobasal cell polarity and also play important roles in the control of cell proliferation, survival, differentiation and in cell migration/invasion. The precise mechanism by which Scribble, Dlg and Lgl function is not clear; however, they have been implicated in the regulation of signalling pathways, vesicle trafficking and in the Myosin II-actin cytoskeleton. We review the evidence for the involvement of Scribble, Dlg, and Lgl in cancer, and how the various functions ascribed to these tumour suppressors in Drosophila and mammalian systems may impact on the process of tumourigenesis.
肿瘤抑制因子Scribble、Dlg和Lgl最初是在黑腹果蝇中发现的,目前人们正在积极研究它们在哺乳动物肿瘤发生中的潜在作用。在果蝇中,这些肿瘤抑制因子在一个共同的遗传途径中发挥作用,以调节顶-基细胞极性,并且在细胞增殖、存活、分化以及细胞迁移/侵袭的控制中也发挥重要作用。Scribble、Dlg和Lgl发挥作用的确切机制尚不清楚;然而,它们与信号通路的调节、囊泡运输以及肌球蛋白II-肌动蛋白细胞骨架有关。我们综述了Scribble、Dlg和Lgl参与癌症的证据,以及在果蝇和哺乳动物系统中赋予这些肿瘤抑制因子的各种功能如何可能影响肿瘤发生过程。