Intron retention is a hallmark and spliceosome represents a therapeutic vulnerability in aggressive prostate cancer

Dysregulation of mRNA alternative splicing is prevalent in cancers. Here, the authors characterized the landscape of aberrant alternative splicing during the development of prostate cancer, progression and therapeutic resistance and show that splicing modulator, E7107, reduces growth in castration-r...

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Autores principales: Dingxiao Zhang, Qiang Hu, Xiaozhuo Liu, Yibing Ji, Hsueh-Ping Chao, Yan Liu, Amanda Tracz, Jason Kirk, Silvia Buonamici, Ping Zhu, Jianmin Wang, Song Liu, Dean G. Tang
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Lenguaje:EN
Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/7650acc90f58486d8e0f1601efde26ba
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spelling oai:doaj.org-article:7650acc90f58486d8e0f1601efde26ba2021-12-02T14:40:38ZIntron retention is a hallmark and spliceosome represents a therapeutic vulnerability in aggressive prostate cancer10.1038/s41467-020-15815-72041-1723https://doaj.org/article/7650acc90f58486d8e0f1601efde26ba2020-04-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-15815-7https://doaj.org/toc/2041-1723Dysregulation of mRNA alternative splicing is prevalent in cancers. Here, the authors characterized the landscape of aberrant alternative splicing during the development of prostate cancer, progression and therapeutic resistance and show that splicing modulator, E7107, reduces growth in castration-resistant prostate cancer.Dingxiao ZhangQiang HuXiaozhuo LiuYibing JiHsueh-Ping ChaoYan LiuAmanda TraczJason KirkSilvia BuonamiciPing ZhuJianmin WangSong LiuDean G. TangNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-19 (2020)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Dingxiao Zhang
Qiang Hu
Xiaozhuo Liu
Yibing Ji
Hsueh-Ping Chao
Yan Liu
Amanda Tracz
Jason Kirk
Silvia Buonamici
Ping Zhu
Jianmin Wang
Song Liu
Dean G. Tang
Intron retention is a hallmark and spliceosome represents a therapeutic vulnerability in aggressive prostate cancer
description Dysregulation of mRNA alternative splicing is prevalent in cancers. Here, the authors characterized the landscape of aberrant alternative splicing during the development of prostate cancer, progression and therapeutic resistance and show that splicing modulator, E7107, reduces growth in castration-resistant prostate cancer.
format article
author Dingxiao Zhang
Qiang Hu
Xiaozhuo Liu
Yibing Ji
Hsueh-Ping Chao
Yan Liu
Amanda Tracz
Jason Kirk
Silvia Buonamici
Ping Zhu
Jianmin Wang
Song Liu
Dean G. Tang
author_facet Dingxiao Zhang
Qiang Hu
Xiaozhuo Liu
Yibing Ji
Hsueh-Ping Chao
Yan Liu
Amanda Tracz
Jason Kirk
Silvia Buonamici
Ping Zhu
Jianmin Wang
Song Liu
Dean G. Tang
author_sort Dingxiao Zhang
title Intron retention is a hallmark and spliceosome represents a therapeutic vulnerability in aggressive prostate cancer
title_short Intron retention is a hallmark and spliceosome represents a therapeutic vulnerability in aggressive prostate cancer
title_full Intron retention is a hallmark and spliceosome represents a therapeutic vulnerability in aggressive prostate cancer
title_fullStr Intron retention is a hallmark and spliceosome represents a therapeutic vulnerability in aggressive prostate cancer
title_full_unstemmed Intron retention is a hallmark and spliceosome represents a therapeutic vulnerability in aggressive prostate cancer
title_sort intron retention is a hallmark and spliceosome represents a therapeutic vulnerability in aggressive prostate cancer
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/7650acc90f58486d8e0f1601efde26ba
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