Sun Yiting, Li Song, Yu Wenbin, Chen Cheng, Liu Teng, Li Lanbo, Zhang Di, Zhao Zeyi, Gao Jing, Wang Xiao, Shi Duanbo, Liu Lian
Department of Medical Oncology, Cancer Center, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, China.
Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100021, China.
J Cancer. 2020 Feb 19;11(9):2667-2678. doi: 10.7150/jca.40955. eCollection 2020.
CD148 is a member of the receptor-type protein tyrosine phosphatase family encoded by the gene and has controversial impacts on cancers. In this study, we investigated the clinical significance of CD148 in gastric cancer and the possible mechanisms. Suppressed CD148 expression indicated adverse pathological features and poor outcomes in gastric cancer patients. CD148 overexpression impeded tumor proliferation, motility, and invasiveness, while CD148 knock-down or knockout promoted the ability of gastric cancer cells to grow and metastasize and . Mechanistically, CD148 negatively regulated EGFR phosphorylation of multiple tyrosine residues, including Y1173, Y1068, and Y1092, and remarkably inhibited downstream PI3K/AKT and MEK/ERK pathways. analysis revealed that gene deletions or missense/truncated mutations of gene rarely occurred in gastric cancers. Instead, a 3' UTR-specific methylation might regulate CD148 expression, and the potential regulators were TET2 and TET3. Collectively, our results suggest that CD148 is a convincing prognostic marker as well as a potential therapeutic target for gastric cancer.
CD148是由该基因编码的受体型蛋白酪氨酸磷酸酶家族的成员,对癌症具有争议性影响。在本研究中,我们调查了CD148在胃癌中的临床意义及可能机制。CD148表达受抑制表明胃癌患者具有不良病理特征和较差预后。CD148过表达阻碍肿瘤增殖、运动及侵袭,而CD148敲低或敲除则促进胃癌细胞生长和转移的能力。机制上,CD148负向调节包括Y1173、Y1068和Y1092在内的多个酪氨酸残基的EGFR磷酸化,并显著抑制下游PI3K/AKT和MEK/ERK途径。分析显示该基因的基因缺失或错义/截短突变在胃癌中很少发生。相反,3' UTR特异性甲基化可能调节CD148表达,潜在调节因子为TET2和TET3。总体而言,我们的结果表明CD148是一个可靠的预后标志物以及胃癌的潜在治疗靶点。