MTR4 drives liver tumorigenesis by promoting cancer metabolic switch through alternative splicing

Aberrant alternative splicing has been shown to contribute to the tumorigenic processes. Here, the authors show that MTR4 is overexpressed in hepatocellular carcinoma and has a role in tumorigenesis through the modulation of the splicing of glycolytic genes PKM2 and GLUT1.

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Autores principales: Lili Yu, Jinchul Kim, Lei Jiang, Bingbing Feng, Yue Ying, Kai-yuan Ji, Qingshuang Tang, Wancheng Chen, Taoyi Mai, Wenlong Dou, Jianlong Zhou, Le-yang Xiang, Yang-fan He, Dinghua Yang, Qingjiao Li, Xuemei Fu, Yang Xu
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Lenguaje:EN
Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/d6f7056973d7420fa80b0b12ab8c2f6e
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spelling oai:doaj.org-article:d6f7056973d7420fa80b0b12ab8c2f6e2021-12-02T14:40:51ZMTR4 drives liver tumorigenesis by promoting cancer metabolic switch through alternative splicing10.1038/s41467-020-14437-32041-1723https://doaj.org/article/d6f7056973d7420fa80b0b12ab8c2f6e2020-02-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-14437-3https://doaj.org/toc/2041-1723Aberrant alternative splicing has been shown to contribute to the tumorigenic processes. Here, the authors show that MTR4 is overexpressed in hepatocellular carcinoma and has a role in tumorigenesis through the modulation of the splicing of glycolytic genes PKM2 and GLUT1.Lili YuJinchul KimLei JiangBingbing FengYue YingKai-yuan JiQingshuang TangWancheng ChenTaoyi MaiWenlong DouJianlong ZhouLe-yang XiangYang-fan HeDinghua YangQingjiao LiXuemei FuYang XuNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-12 (2020)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Lili Yu
Jinchul Kim
Lei Jiang
Bingbing Feng
Yue Ying
Kai-yuan Ji
Qingshuang Tang
Wancheng Chen
Taoyi Mai
Wenlong Dou
Jianlong Zhou
Le-yang Xiang
Yang-fan He
Dinghua Yang
Qingjiao Li
Xuemei Fu
Yang Xu
MTR4 drives liver tumorigenesis by promoting cancer metabolic switch through alternative splicing
description Aberrant alternative splicing has been shown to contribute to the tumorigenic processes. Here, the authors show that MTR4 is overexpressed in hepatocellular carcinoma and has a role in tumorigenesis through the modulation of the splicing of glycolytic genes PKM2 and GLUT1.
format article
author Lili Yu
Jinchul Kim
Lei Jiang
Bingbing Feng
Yue Ying
Kai-yuan Ji
Qingshuang Tang
Wancheng Chen
Taoyi Mai
Wenlong Dou
Jianlong Zhou
Le-yang Xiang
Yang-fan He
Dinghua Yang
Qingjiao Li
Xuemei Fu
Yang Xu
author_facet Lili Yu
Jinchul Kim
Lei Jiang
Bingbing Feng
Yue Ying
Kai-yuan Ji
Qingshuang Tang
Wancheng Chen
Taoyi Mai
Wenlong Dou
Jianlong Zhou
Le-yang Xiang
Yang-fan He
Dinghua Yang
Qingjiao Li
Xuemei Fu
Yang Xu
author_sort Lili Yu
title MTR4 drives liver tumorigenesis by promoting cancer metabolic switch through alternative splicing
title_short MTR4 drives liver tumorigenesis by promoting cancer metabolic switch through alternative splicing
title_full MTR4 drives liver tumorigenesis by promoting cancer metabolic switch through alternative splicing
title_fullStr MTR4 drives liver tumorigenesis by promoting cancer metabolic switch through alternative splicing
title_full_unstemmed MTR4 drives liver tumorigenesis by promoting cancer metabolic switch through alternative splicing
title_sort mtr4 drives liver tumorigenesis by promoting cancer metabolic switch through alternative splicing
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/d6f7056973d7420fa80b0b12ab8c2f6e
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