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细胞应激和氧化还原活性蛋白参与与幽门螺杆菌感染相关的胃癌发生,该感染表达高水平的硫氧还蛋白-1。

Cellular stress and redox activity proteins are involved in gastric carcinogenesis associated with Helicobacter pylori infection expressing high levels of thioredoxin-1.

机构信息

Research Center of Clinical Epidemiology, Peking University Third Hospital, Beijing 100191, China.

Department of Gastroenterology, Peking University Third Hospital, Beijing 100191, China.

出版信息

J Zhejiang Univ Sci B. 2018;19(10):750-763. doi: 10.1631/jzus.B1700456.

Abstract

Helicobacter pylori infection is related to the development of gastric diseases. Our previous studies showed that high thioredoxin-1 (Trx1) expression in H. pylori can promote gastric carcinogenesis. To explore the underlying molecular mechanisms, we performed an isobaric tags for relative and absolute quantitation (iTRAQ)-based quantitative proteomic analysis of stomach tissues from Mongolian gerbil infected with H. pylori expressing high and low Trx1. Differences in the profiles of the expressed proteins were analyzed by bioinformatics and verified using Western blot analysis. We found three candidate proteins, 14-3-3α/β, glutathione-S-transferase (GST), and heat shock protein 70 (HSP70), in high Trx1 tissues compared with low Trx1 tissues and concluded that cellular stress and redox activity-related proteins were involved in the pathogenesis of gastric cancer associated with H. pylori Trx1.

摘要

幽门螺杆菌感染与胃部疾病的发展有关。我们之前的研究表明,幽门螺杆菌中高硫氧还蛋白-1(Trx1)的表达可以促进胃癌的发生。为了探讨潜在的分子机制,我们对感染了高表达和低表达 Trx1 的幽门螺杆菌的蒙古沙鼠的胃组织进行了基于同位素标记相对和绝对定量(iTRAQ)的定量蛋白质组学分析。通过生物信息学分析和 Western blot 分析验证了差异表达蛋白的差异。我们在高 Trx1 组织中发现了三个候选蛋白,即 14-3-3α/β、谷胱甘肽-S-转移酶(GST)和热休克蛋白 70(HSP70),与低 Trx1 组织相比,这表明与细胞应激和氧化还原活性相关的蛋白参与了与幽门螺杆菌 Trx1 相关的胃癌的发病机制。

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