Yim J-H, Kim Y-J, Ko J-H, Cho Y-E, Kim S-M, Kim J-Y, Lee S, Park J-H
Department of Pathology, College of Medicine, Kyung Hee University, Seoul 130-701, Korea.
Cell Death Differ. 2007 Nov;14(11):1872-9. doi: 10.1038/sj.cdd.4402204. Epub 2007 Jul 27.
Glioma tumor suppressor candidate region gene 2 (GLTSCR2/PICT-1) is localized within the well-known 1.4-Mb tumor suppressive region of chromosome 19q, which is frequently altered in various human tumors, including diffuse gliomas. Aside from its localization on the chromosome, several lines of evidence, such as PTEN phosphorylation, support that GLTSCR2 partakes in the suppression of tumor growth and development. However, much remains unknown about the molecular mechanisms of the tumor suppressive activity of GLTSCR2. The purpose of this study was to investigate the molecular mechanisms of GLTSCR2 in cell death pathways in association with its binding partner PTEN. In this work, we show that GLTSCR2 is a nucleus-localized protein with a discrete globular expression pattern. In addition to phosphorylating PTEN, GLTSCR2 induces caspase-independent PTEN-modulated apoptotic cell death when overexpressed. However, the cytotoxic activity of GLTSCR2 is independent of its ability to phosphorylate PTEN, suggesting that the GLTSCR2-induced cell death pathway is divergent from PTEN-induced death pathways. Our results suggest that the induction of PTEN-modulated apoptosis is one of the putative mechanisms of tumor suppressive activity by GLTSCR2.
胶质瘤肿瘤抑制候选区域基因2(GLTSCR2/PICT-1)定位于19号染色体上著名的1.4兆碱基肿瘤抑制区域内,该区域在包括弥漫性胶质瘤在内的各种人类肿瘤中经常发生改变。除了其在染色体上的定位外,诸如PTEN磷酸化等多条证据支持GLTSCR2参与肿瘤生长和发育的抑制。然而,关于GLTSCR2肿瘤抑制活性的分子机制仍有许多未知之处。本研究的目的是研究GLTSCR2在细胞死亡途径中与其结合伴侣PTEN相关的分子机制。在这项工作中,我们表明GLTSCR2是一种具有离散球状表达模式的核定位蛋白。除了使PTEN磷酸化外,GLTSCR2过表达时还会诱导不依赖半胱天冬酶的PTEN调节的凋亡细胞死亡。然而,GLTSCR2的细胞毒性活性与其使PTEN磷酸化的能力无关,这表明GLTSCR2诱导的细胞死亡途径与PTEN诱导的死亡途径不同。我们的结果表明,PTEN调节的凋亡诱导是GLTSCR2肿瘤抑制活性的一种推定机制。