Yu Shuangjin, Li Guanghua, Wang Zhao, Wang Zhixiong, Chen Chuangqi, Cai Shirong, He Yulong
Department of Gastrointestinal Surgery, First Affiliated Hospital of Sun Yat-sen University, No. 58, Zhongshan 2nd Street, Guangzhou, 510080, Guangdong Province, People's Republic of China.
Tumour Biol. 2016 Nov;37(11):15007-15017. doi: 10.1007/s13277-016-5383-5. Epub 2016 Sep 22.
Since the roles of autophagy in gastric cancer remain unclear, we aim to investigate the expression of autophagy-related proteins MAP1LC3B and Beclin-1 in human gastric cancer and discuss their clinical significance and correlation with prognosis of patients with gastric cancer. A total of 160 consecutive patients with gastric cancer who had undergone gastrectomy were enrolled in this study. The expressions of MAP1LC3B and Beclin-1 were assessed by immunohistochemistry. The protein expression rates were analyzed with χ and Fisher's exact tests. Survival analysis (overall survival (OS) and relapse-free survival (RFS)) was determined using the Kaplan-Meier method and Cox's proportional hazard regression model. Both the expressions of MAP1LC3B and Beclin-1 were lower in gastric cancer tissues than adjacent normal tissues (57 vs. 82 %, p = 0.007; 72 vs. 88 %, p = 0.046, respectively). Relativity analysis indicated MAP1LC3B expression was positively correlated with Beclin-1 expression (r = 0.424, p < 0.001). Both the MAP1LC3B-high-expression patients and Beclin-1-high-expression patients have longer OS time and RFS time than MAP1LC3B-low-expression patients and Beclin-1-low-expression patients (MAP1LC3B: both p < 0.001; Beclin-1: p = 0.014, p = 0.015, respectively). High simultaneous MAP1LC3B and Beclin-1 expressions were associated with longer OS and RFS compared with low simultaneous MAP1LC3B and Beclin-1 expressions (56.77 vs. 24.42 months, p < 0.001; 53.56 vs. 22.33 months, p < 0.001, respectively). Multivariate survival analysis showed both MAP1LC3B and Beclin-1 were independent prognostic factors for OS time (p = 0.016, p = 0.041, respectively). However, MAP1LC3B (p = 0.022) was an independent prognostic factor for RFS. Moreover, low expressions of MAP1LC3B and Beclin-1 were significantly associated with lymph node metastasis (p = 0.007, p = 0.030, respectively). The loss of MAP1LC3B, correlated with loss of Beclin-1, was observed in gastric cancer and correlated with poor prognosis and lymph node metastasis of gastric cancer patients.
由于自噬在胃癌中的作用尚不清楚,我们旨在研究自噬相关蛋白MAP1LC3B和Beclin-1在人胃癌中的表达,并探讨其临床意义以及与胃癌患者预后的相关性。本研究共纳入160例连续接受胃切除术的胃癌患者。通过免疫组织化学评估MAP1LC3B和Beclin-1的表达。采用χ检验和Fisher精确检验分析蛋白表达率。使用Kaplan-Meier法和Cox比例风险回归模型进行生存分析(总生存期(OS)和无复发生存期(RFS))。胃癌组织中MAP1LC3B和Beclin-1的表达均低于相邻正常组织(分别为57%对82%,p = 0.007;72%对88%,p = 0.046)。相关性分析表明MAP1LC3B表达与Beclin-1表达呈正相关(r = 0.424,p < 0.001)。MAP1LC3B高表达患者和Beclin-1高表达患者的OS时间和RFS时间均长于MAP1LC3B低表达患者和Beclin-1低表达患者(MAP1LC3B:均p < 0.001;Beclin-1:分别为p = 0.014,p = 0.015)。与MAP1LC3B和Beclin-1低同时表达相比,MAP1LC3B和Beclin-1高同时表达与更长的OS和RFS相关(分别为56.77个月对24.42个月,p < 0.001;53.56个月对22.33个月,p < 0.001)。多因素生存分析显示MAP1LC3B和Beclin-1均为OS时间的独立预后因素(分别为p = 0.016,p = 0.041)。然而,MAP1LC3B(p = 0.022)是RFS的独立预后因素。此外,MAP1LC3B和Beclin-1的低表达与淋巴结转移显著相关(分别为p = 0.007,p = 0.030)。在胃癌中观察到MAP1LC3B的缺失与Beclin-1的缺失相关,并与胃癌患者的不良预后和淋巴结转移相关。