Department of Obstetrics and Gynecology and Division of Cancer Biology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan.
Division of Cancer Biology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan.
Carcinogenesis. 2014 Sep;35(9):1993-2001. doi: 10.1093/carcin/bgu081. Epub 2014 Mar 27.
Pleomorphic adenoma gene like-2 (PLAGL2), a member of the PLAG gene family, is a C2H2 zinc finger transcriptional factor that is involved in cellular transformation and apoptosis. In this report, we show that PLAGL2 is associated with the organization of stress fibers and with small guanosine triphosphatase (GTPase) activity. Depletion of PLAGL2 in two different ovarian cancer cell lines, ES-2 and HEY, induced activation of RhoA, whereas activity of Rac1 was suppressed. Organization of actin stress fibers and focal adhesions was significantly promoted by PLAGL2 knockdown in a RhoA-dependent manner. Conversely, exogenous expression of PLAGL2 in MDA-MB-231 cells, a breast cancer cell line, resulted in the activation of Rac1 and the inactivation of RhoA. In addition, PLAGL2 expression induced lamellipodia formation and disruption of stress fiber formation. Finally, we show that CHN1 expression is essential for Rac1 inactivation in PLAGL2-depleted cells. Our results demonstrate a crucial role of PLAGL2 in actin dynamics and give further insight into the role of PLAGL2 in cellular transformation and apoptosis.
多形性腺瘤基因样 2(PLAGL2)是 PLAG 基因家族的成员,是一种 C2H2 锌指转录因子,参与细胞转化和凋亡。在本报告中,我们表明 PLAGL2 与应激纤维的组织和小 GTP 酶(GTPase)活性有关。在两种不同的卵巢癌细胞系 ES-2 和 HEY 中,PLAGL2 的耗竭诱导了 RhoA 的激活,而 Rac1 的活性受到抑制。PLAGL2 敲低以 RhoA 依赖性方式显著促进肌动蛋白应激纤维和焦点黏附的组织。相反,外源性表达 PLAGL2 在 MDA-MB-231 细胞(乳腺癌细胞系)中导致 Rac1 的激活和 RhoA 的失活。此外,PLAGL2 表达诱导片状伪足的形成和应激纤维形成的破坏。最后,我们表明 CHN1 表达对于 PLAGL2 耗尽细胞中 Rac1 的失活是必需的。我们的结果表明 PLAGL2 在肌动蛋白动力学中起着至关重要的作用,并进一步深入了解 PLAGL2 在细胞转化和凋亡中的作用。