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含铜胺氧化酶1的下调通过抑制肝细胞癌中IL-6/JAK/STAT3信号通路的激活来抑制肿瘤进展。

Downregulation of amine oxidase copper containing 1 inhibits tumor progression by suppressing IL-6/JAK/STAT3 pathway activation in hepatocellular carcinoma.

作者信息

Ding Qian, Lin Dongdong, Zhou Yajing, Li Feng, Lai Jianming, Duan Jianping, Chen Jing, Jiang Caihua

机构信息

Department of Infectious Disease, Qingdao No. 6 People's Hospital, Qingdao, Shandong 266033, P.R. China.

Blood Purification Center, Qingdao No. 6 People's Hospital, Qingdao, Shandong 266033, P.R. China.

出版信息

Oncol Lett. 2021 Dec;22(6):857. doi: 10.3892/ol.2021.13118. Epub 2021 Oct 30.

Abstract

Amine oxidase copper containing 1 (AOC1) is a copper-containing amine oxidase that catalyzes the deamination of polyamines. AOC1 functions as an oncogene in human gastric cancer. There is little information available regarding the function of AOC1 in hepatocellular carcinoma (HCC). In the present study, reverse transcription-quantitative PCR was used to detect the expression levels of AOC1 in HCC tissues, and the role of AOC1 in HCC progression was determined using western blot, Cell Counting Kit 8, clone formation, wound-healing and Transwell assays. An AOC1 survival curve was generated with data downloaded from The Cancer Genome Atlas, and Gene Set Enrichment Analysis was performed to investigate the potential biological mechanisms of AOC1 in HCC. AOC1 was found to be upregulated in HCC tissues, which was associated with a poor prognosis. Furthermore, AOC1-knockdown inhibited HCC cell proliferation, migration and invasiveness, suppressed IL-6 expression, as well as decreasing JAK2 and STAT3 phosphorylation. Ultimately, the results of the present study illustrate that AOC1 promoted the proliferation, migration and invasiveness of HCC cells by regulating the IL-6/JAK/STAT3 pathway.

摘要

含铜胺氧化酶1(AOC1)是一种含铜胺氧化酶,可催化多胺的脱氨反应。AOC1在人类胃癌中作为一种癌基因发挥作用。关于AOC1在肝细胞癌(HCC)中的功能,目前可用信息较少。在本研究中,采用逆转录定量PCR检测HCC组织中AOC1的表达水平,并通过蛋白质印迹法、细胞计数试剂盒8、克隆形成、伤口愈合和Transwell实验确定AOC1在HCC进展中的作用。利用从癌症基因组图谱下载的数据生成AOC1生存曲线,并进行基因集富集分析以研究AOC1在HCC中的潜在生物学机制。研究发现AOC1在HCC组织中上调,这与预后不良相关。此外,敲低AOC1可抑制HCC细胞增殖、迁移和侵袭,抑制IL-6表达,并降低JAK2和STAT3磷酸化水平。最终,本研究结果表明AOC1通过调节IL-6/JAK/STAT3通路促进HCC细胞的增殖、迁移和侵袭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab53/8581477/ba8e47d5d1b2/ol-22-06-13118-g00.jpg

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