Cargando…
Down-regulation of SLC25A20 promotes hepatocellular carcinoma growth and metastasis through suppression of fatty-acid oxidation
Solute carrier family 25 member 20 (SLC25A20) is a mitochondrial-membrane–carrier protein involved in the transport of acylcarnitines into mitochondrial matrix for oxidation. A previous-integrated-proteogenomic study had identified SLC25A20 as one of the top-three prognostic biomarkers in HCC. Howev...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024385/ https://www.ncbi.nlm.nih.gov/pubmed/33824298 http://dx.doi.org/10.1038/s41419-021-03648-1 |
_version_ | 1783675302168231936 |
---|---|
author | Yuan, Peng Mu, Jiao Wang, Zijun Ma, Shuaijun Da, Xiuwei Song, Jian Zhang, Hongxin Yang, Le Li, Jibin Yang, Jingyue |
author_facet | Yuan, Peng Mu, Jiao Wang, Zijun Ma, Shuaijun Da, Xiuwei Song, Jian Zhang, Hongxin Yang, Le Li, Jibin Yang, Jingyue |
author_sort | Yuan, Peng |
collection | PubMed |
description | Solute carrier family 25 member 20 (SLC25A20) is a mitochondrial-membrane–carrier protein involved in the transport of acylcarnitines into mitochondrial matrix for oxidation. A previous-integrated-proteogenomic study had identified SLC25A20 as one of the top-three prognostic biomarkers in HCC. However, the expression and the biological function of SLC25A20 have not yet been investigated in HCC. In the present study, we found that SLC25A20 expression is frequently down-regulated in HCC cells mainly due to the up-regulation of miR-132-3p. Down-regulation of SLC25A20 is associated with a poor prognosis in patients with HCC. SLC25A20 suppressed HCC growth and metastasis, both in vitro and in vivo, by suppression of G1–S cell transition, epithelial-to-mesenchymal transition (EMT), and induction of cell apoptosis. Mechanistically, SLC25A20 down-regulation promoted HCC growth and metastasis through suppression of fatty-acid oxidation. Altogether, SLC25A20 plays a critical tumor-suppressive role in carcinogenesis of HCC; SLC25A20 may serve as a novel prognostic factor and therapeutic target for patients with HCC. |
format | Online Article Text |
id | pubmed-8024385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80243852021-04-21 Down-regulation of SLC25A20 promotes hepatocellular carcinoma growth and metastasis through suppression of fatty-acid oxidation Yuan, Peng Mu, Jiao Wang, Zijun Ma, Shuaijun Da, Xiuwei Song, Jian Zhang, Hongxin Yang, Le Li, Jibin Yang, Jingyue Cell Death Dis Article Solute carrier family 25 member 20 (SLC25A20) is a mitochondrial-membrane–carrier protein involved in the transport of acylcarnitines into mitochondrial matrix for oxidation. A previous-integrated-proteogenomic study had identified SLC25A20 as one of the top-three prognostic biomarkers in HCC. However, the expression and the biological function of SLC25A20 have not yet been investigated in HCC. In the present study, we found that SLC25A20 expression is frequently down-regulated in HCC cells mainly due to the up-regulation of miR-132-3p. Down-regulation of SLC25A20 is associated with a poor prognosis in patients with HCC. SLC25A20 suppressed HCC growth and metastasis, both in vitro and in vivo, by suppression of G1–S cell transition, epithelial-to-mesenchymal transition (EMT), and induction of cell apoptosis. Mechanistically, SLC25A20 down-regulation promoted HCC growth and metastasis through suppression of fatty-acid oxidation. Altogether, SLC25A20 plays a critical tumor-suppressive role in carcinogenesis of HCC; SLC25A20 may serve as a novel prognostic factor and therapeutic target for patients with HCC. Nature Publishing Group UK 2021-04-06 /pmc/articles/PMC8024385/ /pubmed/33824298 http://dx.doi.org/10.1038/s41419-021-03648-1 Text en © The Author(s) 2021 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 Yuan, Peng Mu, Jiao Wang, Zijun Ma, Shuaijun Da, Xiuwei Song, Jian Zhang, Hongxin Yang, Le Li, Jibin Yang, Jingyue Down-regulation of SLC25A20 promotes hepatocellular carcinoma growth and metastasis through suppression of fatty-acid oxidation |
title | Down-regulation of SLC25A20 promotes hepatocellular carcinoma growth and metastasis through suppression of fatty-acid oxidation |
title_full | Down-regulation of SLC25A20 promotes hepatocellular carcinoma growth and metastasis through suppression of fatty-acid oxidation |
title_fullStr | Down-regulation of SLC25A20 promotes hepatocellular carcinoma growth and metastasis through suppression of fatty-acid oxidation |
title_full_unstemmed | Down-regulation of SLC25A20 promotes hepatocellular carcinoma growth and metastasis through suppression of fatty-acid oxidation |
title_short | Down-regulation of SLC25A20 promotes hepatocellular carcinoma growth and metastasis through suppression of fatty-acid oxidation |
title_sort | down-regulation of slc25a20 promotes hepatocellular carcinoma growth and metastasis through suppression of fatty-acid oxidation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024385/ https://www.ncbi.nlm.nih.gov/pubmed/33824298 http://dx.doi.org/10.1038/s41419-021-03648-1 |
work_keys_str_mv | AT yuanpeng downregulationofslc25a20promoteshepatocellularcarcinomagrowthandmetastasisthroughsuppressionoffattyacidoxidation AT mujiao downregulationofslc25a20promoteshepatocellularcarcinomagrowthandmetastasisthroughsuppressionoffattyacidoxidation AT wangzijun downregulationofslc25a20promoteshepatocellularcarcinomagrowthandmetastasisthroughsuppressionoffattyacidoxidation AT mashuaijun downregulationofslc25a20promoteshepatocellularcarcinomagrowthandmetastasisthroughsuppressionoffattyacidoxidation AT daxiuwei downregulationofslc25a20promoteshepatocellularcarcinomagrowthandmetastasisthroughsuppressionoffattyacidoxidation AT songjian downregulationofslc25a20promoteshepatocellularcarcinomagrowthandmetastasisthroughsuppressionoffattyacidoxidation AT zhanghongxin downregulationofslc25a20promoteshepatocellularcarcinomagrowthandmetastasisthroughsuppressionoffattyacidoxidation AT yangle downregulationofslc25a20promoteshepatocellularcarcinomagrowthandmetastasisthroughsuppressionoffattyacidoxidation AT lijibin downregulationofslc25a20promoteshepatocellularcarcinomagrowthandmetastasisthroughsuppressionoffattyacidoxidation AT yangjingyue downregulationofslc25a20promoteshepatocellularcarcinomagrowthandmetastasisthroughsuppressionoffattyacidoxidation |