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PAFAH1B3是一种KLF9靶基因,可促进胰腺癌的增殖和转移。

PAFAH1B3 is a KLF9 target gene that promotes proliferation and metastasis in pancreatic cancer.

作者信息

Dong Cairong, Yao Jinping, Wu Zhipeng, Hu Junwen, Sun Liang, Wu Zhengyi, Yan Jinlong, Yin Xiangbao

机构信息

Department of General Surgery, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi Province, People's Republic of China.

Department of Endocrinology Department, The Fourth Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi Province, People's Republic of China.

出版信息

Sci Rep. 2024 Apr 22;14(1):9196. doi: 10.1038/s41598-024-59427-3.

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal human malignancies. Uncontrolled cell proliferation, invasion and migration of pancreatic cancer cells are the fundamental causes of death in PDAC patients. Our previous studies showed that KLF9 inhibits the proliferation, invasion and migration of pancreatic cancer cells. However, the underlying mechanisms are not fully understood. In this study, we found that platelet-activating factor acetylhydrolase IB3 (PAFAH1B3) is highly expressed in pancreatic cancer tissues and cells. In vitro and in vivo studies showed that overexpression of PAFAH1B3 promoted the proliferation and invasion of pancreatic cancer cells, while downregulation of PAFAH1B3 inhibited these processes. We found that KLF9 expression is negatively correlated with PAFAH1B3 expression in pancreatic cancer tissues and cells. Western blotting revealed that KLF9 negatively regulates the expression of PAFAH1B3 in pancreatic cancer tissues and cells. Rescue experiments showed that overexpression of PAFAH1B3 could partially attenuate the suppression of pancreatic cancer cell proliferation, invasion and migration induced by KLF9 overexpression. Finally, chromatin immunoprecipitation (ChIP) and dual-luciferase reporter assays were carried out, and the results showed that KLF9 directly binds to the promoter of PAFAH1B3 and inhibits its transcriptional activity. In conclusion, our study indicated that KLF9 can inhibit the proliferation, invasion, migration and metastasis of pancreatic cancer cells by inhibiting PAFAH1B3.

摘要

胰腺导管腺癌(PDAC)是最致命的人类恶性肿瘤之一。胰腺癌细胞不受控制的细胞增殖、侵袭和迁移是PDAC患者死亡的根本原因。我们之前的研究表明,KLF9抑制胰腺癌细胞的增殖、侵袭和迁移。然而,其潜在机制尚未完全明确。在本研究中,我们发现血小板活化因子乙酰水解酶IB3(PAFAH1B3)在胰腺癌组织和细胞中高表达。体外和体内研究表明,PAFAH1B3的过表达促进了胰腺癌细胞的增殖和侵袭,而PAFAH1B3的下调则抑制了这些过程。我们发现,在胰腺癌组织和细胞中,KLF9的表达与PAFAH1B3的表达呈负相关。蛋白质免疫印迹法显示,KLF9在胰腺癌组织和细胞中负向调节PAFAH1B3的表达。挽救实验表明,PAFAH1B3的过表达可部分减弱KLF9过表达对胰腺癌细胞增殖、侵袭和迁移的抑制作用。最后,进行了染色质免疫沉淀(ChIP)和双荧光素酶报告基因检测,结果表明KLF9直接结合PAFAH1B3的启动子并抑制其转录活性。总之,我们的研究表明,KLF9可通过抑制PAFAH1B3来抑制胰腺癌细胞的增殖、侵袭、迁移和转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fd7/11035664/ab20affffcc0/41598_2024_59427_Fig1_HTML.jpg

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