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TMPRSS4通过激活ERK1/2信号通路促进胰腺导管腺癌的细胞增殖并抑制细胞凋亡。

TMPRSS4 Promotes Cell Proliferation and Inhibits Apoptosis in Pancreatic Ductal Adenocarcinoma by Activating ERK1/2 Signaling Pathway.

作者信息

Gu Jianyou, Huang Wenjie, Zhang Junfeng, Wang Xianxing, Tao Tian, Yang Ludi, Zheng Yao, Liu Songsong, Yang Jiali, Zhu Liwei, Wang Huaizhi, Fan Yingfang

机构信息

Department of Hepatobiliary Surgery I, Zhujiang Hospital, Southern Medical University, Guangzhou, China.

Institute of Hepatopancreatobiliary Surgery, Chongqing General Hospital, University of Chinese Academy of Sciences, Chongqing, China.

出版信息

Front Oncol. 2021 Mar 18;11:628353. doi: 10.3389/fonc.2021.628353. eCollection 2021.

Abstract

Transmembrane protease serine 4 (TMPRSS4) is upregulated in various kinds of human cancers, including pancreatic cancer. However, its biological function in pancreatic ductal adenocarcinoma (PDAC) remains unclear. In the current study, real-time qPCR, immunohistochemical staining, Western blotting, and database (Cancer Genome Atlas and Gene Expression) analysis revealed remarkable overexpression of TMPRSS4 in PDAC tissue as compared to non-tumor tissue. The TMPRSS4 overexpression was associated with poor prognosis of PDAC patients. Moreover, multivariate analysis revealed that TMPRSS4 serves as an independent risk factor in PDAC. We performed gain-and loss-of-function analysis and found that TMPRSS4 promotes cellular proliferation and inhibits apoptosis of PDAC cells both and . Furthermore, we showed that TMPRSS4 might promote cell proliferation and inhibit apoptosis through activating ERK1/2 signaling pathway in pancreatic cancer cells. These findings were validated by using ERK1/2 phosphorylation inhibitor SCH772984 both and . Taken together, this study suggests that TMPRSS4 is a proto-oncogene, which promotes initiation and progression of PDAC by controlling cell proliferation and apoptosis. Our findings indicate that TMPRSS4 could be a promising prognostic biomarker and a therapeutic target for the treatment of pancreatic cancer.

摘要

跨膜蛋白酶丝氨酸4(TMPRSS4)在包括胰腺癌在内的多种人类癌症中上调。然而,其在胰腺导管腺癌(PDAC)中的生物学功能仍不清楚。在本研究中,实时定量PCR、免疫组织化学染色、蛋白质印迹法和数据库(癌症基因组图谱和基因表达)分析显示,与非肿瘤组织相比,TMPRSS4在PDAC组织中显著过表达。TMPRSS4过表达与PDAC患者的不良预后相关。此外,多变量分析显示TMPRSS4是PDAC的一个独立危险因素。我们进行了功能获得和功能丧失分析,发现TMPRSS4在体内和体外均促进PDAC细胞的增殖并抑制其凋亡。此外,我们表明TMPRSS4可能通过激活胰腺癌细胞中的ERK1/2信号通路来促进细胞增殖并抑制凋亡。使用ERK1/2磷酸化抑制剂SCH772984在体内和体外均验证了这些发现。综上所述,本研究表明TMPRSS4是一种原癌基因,通过控制细胞增殖和凋亡促进PDAC的发生和发展。我们的研究结果表明,TMPRSS4可能是一种有前景的预后生物标志物和胰腺癌治疗的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ece/8012900/6e044ec538ea/fonc-11-628353-g0001.jpg

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