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与低水平的Beclin-1相关的微管相关蛋白1轻链3β(MAP1LC3B)低表达预示着胃癌的淋巴结转移和不良预后。

Low expression of MAP1LC3B, associated with low Beclin-1, predicts lymph node metastasis and poor prognosis of gastric cancer.

作者信息

Yu Shuangjin, Li Guanghua, Wang Zhao, Wang Zhixiong, Chen Chuangqi, Cai Shirong, He Yulong

机构信息

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.

出版信息

Tumour Biol. 2016 Nov;37(11):15007-15017. doi: 10.1007/s13277-016-5383-5. Epub 2016 Sep 22.

Abstract

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.

摘要

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。

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