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E3泛素连接酶通过介导上皮-间质转化促进胃癌细胞转移。

E3 ubiquitin ligase promotes metastasis of gastric cancer cells by mediating epithelial-mesenchymal transition.

作者信息

Li Wei-Wei, Yuan Hao, Kong Shuai, Tian Shu-Bo

机构信息

Department of Pulmonary and Critical Care Medicine, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan 250021, Shandong Province, China.

Department of Critical Care Medicine, The 960 Hospital of the People's Liberation Army Joint Logistics Support Force, Jinan 250031, Shandong Province, China.

出版信息

World J Gastrointest Oncol. 2022 Nov 15;14(11):2183-2194. doi: 10.4251/wjgo.v14.i11.2183.

Abstract

BACKGROUND

Gastric cancer (GC) is considered a major global health problem. The role of TRIM55, a member of the three-domain protein family, in GC is unknown.

AIM

To determine the expression of in GC tissues and its relationship with clinicopathological characteristics, and to investigate the effects of on the malignant biological behavior of GC cells.

METHODS

Differential expression of in GC and para-cancer tissues was detected by immunohistochemistry, and the relationship between level and clinicopathological characteristics and prognosis was analyzed. Gain-of-function, loss-of-function, cell counting kit-8 assay, colony formation, transwell assay, wound healing assay, and western blot analysis were used to assess the potential role of in the development of GC.

RESULTS

expression was significantly increased in GC tissues compared with adjacent normal tissues. High expression of was associated with advanced pathological stage and poor prognosis. Overexpression of promoted invasion and metastasis of GC cells by regulating epithelial-mesenchymal transition (EMT), whereas knockdown of had the opposite effect. Our data showed that is highly expressed in GC tissues, and is associated with poor prognosis. plays the role of an oncogene in GC, and it promotes metastasis of GC through the regulation of EMT.

CONCLUSION

may be a possible target for the diagnosis and prognosis of GC patients.

摘要

背景

胃癌(GC)被认为是一个主要的全球健康问题。三结构域蛋白家族成员TRIM55在胃癌中的作用尚不清楚。

目的

确定TRIM55在胃癌组织中的表达及其与临床病理特征的关系,并研究TRIM55对胃癌细胞恶性生物学行为的影响。

方法

采用免疫组织化学检测TRIM55在胃癌及癌旁组织中的差异表达,并分析TRIM55水平与临床病理特征及预后的关系。运用功能获得、功能缺失、细胞计数试剂盒-8检测、集落形成、Transwell检测、伤口愈合检测及蛋白质印迹分析来评估TRIM55在胃癌发生发展中的潜在作用。

结果

与相邻正常组织相比,胃癌组织中TRIM55表达显著增加。TRIM55高表达与病理分期晚及预后差相关。TRIM55过表达通过调节上皮-间质转化(EMT)促进胃癌细胞的侵袭和转移,而敲低TRIM55则产生相反的效果。我们的数据表明,TRIM55在胃癌组织中高表达,且与预后不良相关。TRIM55在胃癌中起癌基因作用,并通过调节EMT促进胃癌转移。

结论

TRIM55可能是胃癌患者诊断和预后的一个潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd16/9694263/088842a84ab0/WJGO-14-2183-g001.jpg

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