Dai Faxiang, Xuan Yi, Jin Jie-Jie, Yu Shengjia, Long Zi-Wen, Cai Hong, Liu Xiao-Wen, Zhou Ye, Wang Ya-Nong, Chen Zhong, Huang Hua
Department of Gastric Cancer and Soft Tissue Sarcoma, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China.
Oncotarget. 2017 Apr 25;8(17):28736-28749. doi: 10.18632/oncotarget.15661.
C-terminal binding protein-2 (CtBP2), a transcriptional corepressor, has been reported to correlate with tumorigenesis and progression and predict a poor prognosis in several human cancers. However, few studies on CtBP2 in gastric cancer (GC) have been performed. In this research, we evaluated the correlations between CtBP2 expression and the clinicopathological characteristics, as well as prognosis of GC patients. The effects of silencing CtBP2 expression on GC cells biology activity were also assessed. The results showed that CtBP2 was overexpressed in GC tissues and closely correlated with poor differentiation, advanced tumor stage and poor prognosis in GC patients. CtBP2 induced epithelial-to-mesenchymal transition (EMT) and repressed PTEN to increase proliferation rate, migration, and invasion in GC cells. Silencing CtBP2 inhibited GC growth in nude mice model. In conclusion, CtBP2 is overexpressed in GC and may accelerate GC tumorigenesis and metastasis, which could represent an independent prognostic marker and promising therapeutic target for GC.
C 末端结合蛋白 2(CtBP2)是一种转录共抑制因子,据报道它与肿瘤发生和进展相关,并可预测多种人类癌症的不良预后。然而,关于 CtBP2 在胃癌(GC)中的研究较少。在本研究中,我们评估了 CtBP2 表达与 GC 患者临床病理特征以及预后之间的相关性。还评估了沉默 CtBP2 表达对 GC 细胞生物学活性的影响。结果表明,CtBP2 在 GC 组织中过表达,且与 GC 患者的低分化、肿瘤晚期和不良预后密切相关。CtBP2 诱导上皮-间质转化(EMT)并抑制 PTEN,以增加 GC 细胞的增殖率、迁移和侵袭能力。沉默 CtBP2 可抑制裸鼠模型中的 GC 生长。总之,CtBP2 在 GC 中过表达,可能加速 GC 的肿瘤发生和转移,这可能代表一种独立的预后标志物以及 GC 有前景的治疗靶点。