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Proteomics-Based Identification and Analysis of Proteins Associated with Helicobacter pylori in Gastric Cancer

机译:基于蛋白质组学的胃癌幽门螺杆菌相关蛋白的鉴定与分析

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摘要

Helicobacter pylori (H. pylori) is a spiral-shaped Gram-negative bacterium that causes the most common chronic infection in the human stomach. Approximately 1%-3% of infected individuals develop gastric cancer. However, the mechanisms by which H. pylori induces gastric cancer are not completely understood. The available evidence indicates a strong link between the virulence factor of H. pylori, cytotoxin-associated gene A (CagA), and gastric cancer. To further characterize H. pylori virulence, we established three cell lines by infecting the gastric cancer cell lines SGC-7901 and AGS with cagA+ H. pylori and transfecting SGC-7901 with a vector carrying the full-length cagA gene. We detected 135 differently expressed proteins from the three cell lines using proteome technology, and 10 differential proteins common to the three cell lines were selected and identified by LC-MS/MS as well as verified by western blot: β-actin, L-lactate dehydrogenase (LDH), dihydrolipoamide dehydrogenase (DLD), pre-mRNA-processing factor 19 homolog (PRPF19), ATP synthase, calmodulin (CaM), p64 CLCP, Ran-specific GTPase-activating protein (RanGAP), P43 and calreticulin. Detection of the expression of these proteins and genes encoding these proteins in human gastric cancer tissues by real-time PCR (RT-qPCR) and western blot revealed that the expression of β-ACTIN, LDH, DLD, PRPF19 and CaM genes were up-regulated and RanGAP was down-regulated in gastric cancer tissues and/or metastatic lymph nodes compared to peri-cancerous tissues. High gene expression was observed for H. pylori infection in gastric cancer tissues. Furthermore, the LDH, DLD and CaM genes were demethylated at the promoter -2325, -1885 and -276 sites, respectively, and the RanGAP gene was highly methylated at the promoter -570 and -170 sites in H. pylori-infected and cagA-overexpressing cells. These results provide new insights into the molecular pathogenesis and treatment targets for gastric cancer with H. pylori infection.
机译:幽门螺杆菌(H. pylori)是一种螺旋形革兰氏阴性细菌,可引起人胃中最常见的慢性感染。大约1%-3%的感染个体会患上胃癌。但是,尚不完全了解幽门螺杆菌诱发胃癌的机制。现有证据表明幽门螺杆菌的毒力因子,与细胞毒素相关的基因A(CagA)和胃癌之间有很强的联系。为了进一步表征幽门螺杆菌的毒力,我们通过用cagA + 幽门螺杆菌感染胃癌细胞SGC-7901和AGS,并用携带完整的幽门螺杆菌的载体转染SGC-7901来建立三种细胞系长度cagA基因。我们使用蛋白质组技术从这三种细胞系中检测到135种差异表达的蛋白质,并选择了三种细胞系共有的10种差异蛋白质,并通过LC-MS / MS进行了鉴定,并通过Western印迹法进行了验证:β-肌动蛋白,L-乳酸脱氢酶(LDH),二氢脂酰胺脱氢酶(DLD),mRNA加工前因子19同源物(PRPF19),ATP合酶,钙调蛋白(CaM),p64 CLCP,Ran特异性GTPase激活蛋白(RanGAP),P43和钙网蛋白。通过实时荧光定量PCR(RT-qPCR)和蛋白质印迹法检测人胃癌组织中这些蛋白质的表达和编码这些蛋白质的基因,发现β-ACTIN,LDH, DLD ,与癌周癌相比,胃癌组织和/或转移性淋巴结中的 PRPF19 CaM 基因上调,而 RanGAP 下调组织。观察到 H 的高基因表达。胃癌组织中的 pylori 感染。此外, LDH DLD CaM 基因分别在启动子-2325,-1885和-276位脱甲基,而 em> RanGAP 基因在 H 中的启动子-570和-170位高度甲基化。感染了 pylori cagA 的细胞。这些结果为 H 胃癌的分子发病机理和治疗靶点提供了新的见解。 pylori 感染。

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