Xu X, Li W, Fan X, Liang Y, Zhao M, Zhang J, Liang Y, Tong W, Wang J, Yang W, Lu Y
Laboratory of Molecular Oncology, Beijing Institute for Cancer Research, School of Oncology, Peking University, Hai-Dian District, Beijing, China.
Oncogene. 2007 Nov 15;26(52):7371-9. doi: 10.1038/sj.onc.1210538. Epub 2007 May 21.
Multiple genetic alterations are attributed to gastric cancer (GC); however, only a few critical genes have been identified so far. In this study, we isolated and characterized a novel gene p42.3, represented as tumor-specific and mitosis phase-dependent expression protein in GC cell line BGC823. Our data showed that the expression of p42.3 was cell cycle-dependent in GC cell lines. Moreover, p42.3 was specifically expressed in primary GC tissues but not in the matched normal mucosa of stomach, and this gene was expressed in diverse embryonic tissues. Furthermore, significant suppression of cell proliferation and tumorigenicity were detected and G(2)/M phase arrest was observed in cell line BGC823 depleted of p42.3 expression by RNAi technique, and we confirmed the expression changes of cyclin B1 and Chk2 following the silence of p42.3. Taken together, we cloned and characterized p42.3 gene that was specifically expressed in GC tumors but not in normal gastric mucosa, and the gene was associated with M-phase regulation. Moreover, p42.3 might be involved in cell proliferation and tumorigenesis; therefore, this gene might have potential applications in the diagnosis or treatment of GC.
多种基因改变与胃癌(GC)相关;然而,到目前为止仅鉴定出少数关键基因。在本研究中,我们分离并鉴定了一个新基因p42.3,其在GC细胞系BGC823中表现为肿瘤特异性和有丝分裂期依赖性表达蛋白。我们的数据表明,p42.3的表达在GC细胞系中依赖于细胞周期。此外,p42.3在原发性GC组织中特异性表达,但在匹配的胃正常黏膜中不表达,且该基因在多种胚胎组织中表达。此外,通过RNAi技术使细胞系BGC823中p42.3表达缺失后,检测到细胞增殖和致瘤性受到显著抑制,并观察到G(2)/M期阻滞,且我们证实了p42.3沉默后细胞周期蛋白B1和Chk2的表达变化。综上所述,我们克隆并鉴定了在GC肿瘤中特异性表达但在正常胃黏膜中不表达的p42.3基因,该基因与M期调控相关。此外,p42.3可能参与细胞增殖和肿瘤发生;因此,该基因可能在GC的诊断或治疗中具有潜在应用价值。