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Mechanisms of carcinogenic activity triggered by lysine-specific demethylase 1A

Epigenetics has emerged as a prime focus area in the field of cancer research. Lysine-specific demethylase 1A (LSD1), the first discovered histone demethylase, is mainly responsible for catalysing demethylation of histone 3 lysine 4 (H3K4) and H3K9 to activate or inhibit gene transcription. LSD1 is...

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Autores principales: Yang, Chao, Li, Dan, Zang, Shaohong, Zhang, Lei, Zhong, Zhangfeng, Zhou, Yingtang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428822/
https://www.ncbi.nlm.nih.gov/pubmed/36059955
http://dx.doi.org/10.3389/fphar.2022.955218
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author Yang, Chao
Li, Dan
Zang, Shaohong
Zhang, Lei
Zhong, Zhangfeng
Zhou, Yingtang
author_facet Yang, Chao
Li, Dan
Zang, Shaohong
Zhang, Lei
Zhong, Zhangfeng
Zhou, Yingtang
author_sort Yang, Chao
collection PubMed
description Epigenetics has emerged as a prime focus area in the field of cancer research. Lysine-specific demethylase 1A (LSD1), the first discovered histone demethylase, is mainly responsible for catalysing demethylation of histone 3 lysine 4 (H3K4) and H3K9 to activate or inhibit gene transcription. LSD1 is abnormally expressed in various cancers and participates in cancer proliferation, apoptosis, metastasis, invasion, drug resistance and other processes by interacting with regulatory factors. Therefore, it may serve as a potential therapeutic target for cancer. This review summarises the major oncogenic mechanisms mediated by LSD1 and provides a reference for developing novel and efficient anticancer strategies targeting LSD1.
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spelling pubmed-94288222022-09-01 Mechanisms of carcinogenic activity triggered by lysine-specific demethylase 1A Yang, Chao Li, Dan Zang, Shaohong Zhang, Lei Zhong, Zhangfeng Zhou, Yingtang Front Pharmacol Pharmacology Epigenetics has emerged as a prime focus area in the field of cancer research. Lysine-specific demethylase 1A (LSD1), the first discovered histone demethylase, is mainly responsible for catalysing demethylation of histone 3 lysine 4 (H3K4) and H3K9 to activate or inhibit gene transcription. LSD1 is abnormally expressed in various cancers and participates in cancer proliferation, apoptosis, metastasis, invasion, drug resistance and other processes by interacting with regulatory factors. Therefore, it may serve as a potential therapeutic target for cancer. This review summarises the major oncogenic mechanisms mediated by LSD1 and provides a reference for developing novel and efficient anticancer strategies targeting LSD1. Frontiers Media S.A. 2022-07-19 /pmc/articles/PMC9428822/ /pubmed/36059955 http://dx.doi.org/10.3389/fphar.2022.955218 Text en Copyright © 2022 Yang, Li, Zang, Zhang, Zhong and Zhou. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Yang, Chao
Li, Dan
Zang, Shaohong
Zhang, Lei
Zhong, Zhangfeng
Zhou, Yingtang
Mechanisms of carcinogenic activity triggered by lysine-specific demethylase 1A
title Mechanisms of carcinogenic activity triggered by lysine-specific demethylase 1A
title_full Mechanisms of carcinogenic activity triggered by lysine-specific demethylase 1A
title_fullStr Mechanisms of carcinogenic activity triggered by lysine-specific demethylase 1A
title_full_unstemmed Mechanisms of carcinogenic activity triggered by lysine-specific demethylase 1A
title_short Mechanisms of carcinogenic activity triggered by lysine-specific demethylase 1A
title_sort mechanisms of carcinogenic activity triggered by lysine-specific demethylase 1a
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428822/
https://www.ncbi.nlm.nih.gov/pubmed/36059955
http://dx.doi.org/10.3389/fphar.2022.955218
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