Cargando…

microRNA-199a-3p inhibits hepatic apoptosis and hepatocarcinogenesis by targeting PDCD4

Hepatic apoptosis and the initiated liver inflammation play the initial roles in inflammation-induced hepatocarcinogenesis. Molecular mechanisms underlying the regulation of hepatocyte apoptosis and their roles in hepatocarcinogenesis have attracted much attention. A set of microRNAs (miRNAs) have b...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Zhenyang, Zhou, Ye, Zhang, Liyuan, Jia, Kaiwei, Wang, Suyuan, Wang, Mu, Li, Nan, Yu, Yizhi, Cao, Xuetao, Hou, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7585580/
https://www.ncbi.nlm.nih.gov/pubmed/33099584
http://dx.doi.org/10.1038/s41389-020-00282-y
_version_ 1783599823701671936
author Li, Zhenyang
Zhou, Ye
Zhang, Liyuan
Jia, Kaiwei
Wang, Suyuan
Wang, Mu
Li, Nan
Yu, Yizhi
Cao, Xuetao
Hou, Jin
author_facet Li, Zhenyang
Zhou, Ye
Zhang, Liyuan
Jia, Kaiwei
Wang, Suyuan
Wang, Mu
Li, Nan
Yu, Yizhi
Cao, Xuetao
Hou, Jin
author_sort Li, Zhenyang
collection PubMed
description Hepatic apoptosis and the initiated liver inflammation play the initial roles in inflammation-induced hepatocarcinogenesis. Molecular mechanisms underlying the regulation of hepatocyte apoptosis and their roles in hepatocarcinogenesis have attracted much attention. A set of microRNAs (miRNAs) have been determined to be dysregulated in hepatocellular carcinoma (HCC) and participated in cancer progression, however, the roles of these dysregulated miRNAs in carcinogenesis are still poorly understood. We previously analyzed the dysregulated miRNAs in HCC using high-throughput sequencing, and found that miR-199a/b-3p was abundantly expressed in human normal liver while markedly decreased in HCC, which promotes HCC progression. Whether miR-199a/b-3p participates in HCC carcinogenesis is still unknown up to now. Hence, we focused on the role and mechanism of miR-199a/b-3p in hepatocarcinogenesis in this study. Hepatic miR-199a/b-3p was determined to be expressed by miR-199a-2 gene in mice, and we constructed miR-199a-2 knockout and hepatocyte-specific miR-199a-2 knockout mice. Diethylnitrosamine (DEN)-induced hepatocarcinogenesis were markedly increased by hepatocyte-specific miR-199a-3p knockout, which is mediated by the enhanced hepatocyte apoptosis and hepatic injury by DEN administration. In acetaminophen (APAP)-induced acute hepatic injury model, hepatocyte-specific miR-199a-3p knockout also aggravated hepatic apoptosis. By proteomic screening and reporter gene validation, we identified and verified that hepatic programed cell death 4 (PDCD4), which promotes apoptosis, was directly targeted by miR-199a-3p. Furthermore, we confirmed that miR-199a-3p-suppressed hepatocyte apoptosis and hepatic injury by targeting and suppressing PDCD4. Thus, hepatic miR-199a-3p inhibits hepatocyte apoptosis and hepatocarcinogenesis, and decreased miR-199a-3p in hepatocytes may aggravate hepatic injury and HCC development.
format Online
Article
Text
id pubmed-7585580
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-75855802020-10-26 microRNA-199a-3p inhibits hepatic apoptosis and hepatocarcinogenesis by targeting PDCD4 Li, Zhenyang Zhou, Ye Zhang, Liyuan Jia, Kaiwei Wang, Suyuan Wang, Mu Li, Nan Yu, Yizhi Cao, Xuetao Hou, Jin Oncogenesis Article Hepatic apoptosis and the initiated liver inflammation play the initial roles in inflammation-induced hepatocarcinogenesis. Molecular mechanisms underlying the regulation of hepatocyte apoptosis and their roles in hepatocarcinogenesis have attracted much attention. A set of microRNAs (miRNAs) have been determined to be dysregulated in hepatocellular carcinoma (HCC) and participated in cancer progression, however, the roles of these dysregulated miRNAs in carcinogenesis are still poorly understood. We previously analyzed the dysregulated miRNAs in HCC using high-throughput sequencing, and found that miR-199a/b-3p was abundantly expressed in human normal liver while markedly decreased in HCC, which promotes HCC progression. Whether miR-199a/b-3p participates in HCC carcinogenesis is still unknown up to now. Hence, we focused on the role and mechanism of miR-199a/b-3p in hepatocarcinogenesis in this study. Hepatic miR-199a/b-3p was determined to be expressed by miR-199a-2 gene in mice, and we constructed miR-199a-2 knockout and hepatocyte-specific miR-199a-2 knockout mice. Diethylnitrosamine (DEN)-induced hepatocarcinogenesis were markedly increased by hepatocyte-specific miR-199a-3p knockout, which is mediated by the enhanced hepatocyte apoptosis and hepatic injury by DEN administration. In acetaminophen (APAP)-induced acute hepatic injury model, hepatocyte-specific miR-199a-3p knockout also aggravated hepatic apoptosis. By proteomic screening and reporter gene validation, we identified and verified that hepatic programed cell death 4 (PDCD4), which promotes apoptosis, was directly targeted by miR-199a-3p. Furthermore, we confirmed that miR-199a-3p-suppressed hepatocyte apoptosis and hepatic injury by targeting and suppressing PDCD4. Thus, hepatic miR-199a-3p inhibits hepatocyte apoptosis and hepatocarcinogenesis, and decreased miR-199a-3p in hepatocytes may aggravate hepatic injury and HCC development. Nature Publishing Group UK 2020-10-24 /pmc/articles/PMC7585580/ /pubmed/33099584 http://dx.doi.org/10.1038/s41389-020-00282-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Li, Zhenyang
Zhou, Ye
Zhang, Liyuan
Jia, Kaiwei
Wang, Suyuan
Wang, Mu
Li, Nan
Yu, Yizhi
Cao, Xuetao
Hou, Jin
microRNA-199a-3p inhibits hepatic apoptosis and hepatocarcinogenesis by targeting PDCD4
title microRNA-199a-3p inhibits hepatic apoptosis and hepatocarcinogenesis by targeting PDCD4
title_full microRNA-199a-3p inhibits hepatic apoptosis and hepatocarcinogenesis by targeting PDCD4
title_fullStr microRNA-199a-3p inhibits hepatic apoptosis and hepatocarcinogenesis by targeting PDCD4
title_full_unstemmed microRNA-199a-3p inhibits hepatic apoptosis and hepatocarcinogenesis by targeting PDCD4
title_short microRNA-199a-3p inhibits hepatic apoptosis and hepatocarcinogenesis by targeting PDCD4
title_sort microrna-199a-3p inhibits hepatic apoptosis and hepatocarcinogenesis by targeting pdcd4
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7585580/
https://www.ncbi.nlm.nih.gov/pubmed/33099584
http://dx.doi.org/10.1038/s41389-020-00282-y
work_keys_str_mv AT lizhenyang microrna199a3pinhibitshepaticapoptosisandhepatocarcinogenesisbytargetingpdcd4
AT zhouye microrna199a3pinhibitshepaticapoptosisandhepatocarcinogenesisbytargetingpdcd4
AT zhangliyuan microrna199a3pinhibitshepaticapoptosisandhepatocarcinogenesisbytargetingpdcd4
AT jiakaiwei microrna199a3pinhibitshepaticapoptosisandhepatocarcinogenesisbytargetingpdcd4
AT wangsuyuan microrna199a3pinhibitshepaticapoptosisandhepatocarcinogenesisbytargetingpdcd4
AT wangmu microrna199a3pinhibitshepaticapoptosisandhepatocarcinogenesisbytargetingpdcd4
AT linan microrna199a3pinhibitshepaticapoptosisandhepatocarcinogenesisbytargetingpdcd4
AT yuyizhi microrna199a3pinhibitshepaticapoptosisandhepatocarcinogenesisbytargetingpdcd4
AT caoxuetao microrna199a3pinhibitshepaticapoptosisandhepatocarcinogenesisbytargetingpdcd4
AT houjin microrna199a3pinhibitshepaticapoptosisandhepatocarcinogenesisbytargetingpdcd4