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诱导颗粒蛋白促进胃上皮细胞周期进展通过调节 CDK4。

-Induced Progranulin Promotes the Progression of the Gastric Epithelial Cell Cycle by Regulating CDK4.

机构信息

Department of Pathogenic Microbiology, Basic Medical College, Weifang Medical University, Weifang 261053, Shandong, P.R. China.

Key Lab for Immunology in Universities of Shandong Province, Basic Medical College, Weifang Medical University, Weifang 261053, Shandong, P.R. China.

出版信息

J Microbiol Biotechnol. 2022 Jul 28;32(7):844-854. doi: 10.4014/jmb.2203.03053. Epub 2022 Jun 20.

Abstract

, a group 1 carcinogen, colonizes the stomach and affects the development of stomach diseases. Progranulin (PGRN) is an autocrine growth factor that regulates multiple cellular processes and plays a tumorigenic role in many tissues. Nevertheless, the mechanism of action of PGRN in gastric cancer caused by infection remains unclear. Here, we investigated the role of PGRN in cell cycle progression and the cell proliferation induced by infection. We found that the increased PGRN was positively associated with CDK4 expression in gastric cancer tissue. PGRN was upregulated by infection, thereby promoting cell proliferation, and that enhanced level of proliferation was reduced by PGRN inhibitor. CDK4, a target gene of PGRN, is a cyclin-dependent kinase that binds to cyclin D to promote cell cycle progression, which was upregulated by infection. We also showed that knockdown of CDK4 reduced the higher cell cycle progression caused by upregulated PGRN. Moreover, when the PI3K/Akt signaling pathway (which is promoted by PGRN) was blocked, the upregulation of CDK4 mediated by PGRN was reduced. These results reveal the potential mechanism by which PGRN plays a major role through CDK4 in the pathological mechanism of infection.

摘要

幽门螺杆菌,一种 1 类致癌物质,定植于胃部并影响胃部疾病的发展。颗粒体蛋白聚糖(PGRN)是一种自分泌生长因子,调节多种细胞过程,并在许多组织中发挥致癌作用。然而,感染引起的胃癌中 PGRN 的作用机制尚不清楚。在这里,我们研究了 PGRN 在细胞周期进展和 感染诱导的细胞增殖中的作用。我们发现,胃癌组织中 PGRN 的增加与 CDK4 表达呈正相关。感染会导致 PGRN 上调,从而促进细胞增殖,而 PGRN 抑制剂则降低了增殖水平的增强。CDK4 是 PGRN 的靶基因,是一种细胞周期蛋白依赖性激酶,与细胞周期蛋白 D 结合促进细胞周期进展,而这种基因的表达会受到感染的上调。我们还表明,敲低 CDK4 可降低由上调的 PGRN 引起的更高的细胞周期进展。此外,当 PI3K/Akt 信号通路(受 PGRN 促进)被阻断时,PGRN 介导的 CDK4 上调减少。这些结果揭示了 PGRN 通过 CDK4 在 感染病理机制中发挥主要作用的潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2436/9628913/61642a32480c/jmb-32-7-844-f1.jpg

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