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Lung Cancer Therapy Targeting Histone Methylation: Opportunities and Challenges

Lung cancer is one of the most common malignancies. In spite of the progress made in past decades, further studies to improve current therapy for lung cancer are required. Dynamically controlled by methyltransferases and demethylases, methylation of lysine and arginine residues on histone proteins r...

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Detalles Bibliográficos
Autores principales: Chen, Yuchen, Liu, Xinran, Li, Yangkai, Quan, Chuntao, Zheng, Ling, Huang, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039709/
https://www.ncbi.nlm.nih.gov/pubmed/30002791
http://dx.doi.org/10.1016/j.csbj.2018.06.001
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author Chen, Yuchen
Liu, Xinran
Li, Yangkai
Quan, Chuntao
Zheng, Ling
Huang, Kun
author_facet Chen, Yuchen
Liu, Xinran
Li, Yangkai
Quan, Chuntao
Zheng, Ling
Huang, Kun
author_sort Chen, Yuchen
collection PubMed
description Lung cancer is one of the most common malignancies. In spite of the progress made in past decades, further studies to improve current therapy for lung cancer are required. Dynamically controlled by methyltransferases and demethylases, methylation of lysine and arginine residues on histone proteins regulates chromatin organization and thereby gene transcription. Aberrant alterations of histone methylation have been demonstrated to be associated with the progress of multiple cancers including lung cancer. Inhibitors of methyltransferases and demethylases have exhibited anti-tumor activities in lung cancer, and multiple lead candidates are under clinical trials. Here, we summarize how histone methylation functions in lung cancer, highlighting most recent progresses in small molecular inhibitors for lung cancer treatment.
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spelling pubmed-60397092018-07-12 Lung Cancer Therapy Targeting Histone Methylation: Opportunities and Challenges Chen, Yuchen Liu, Xinran Li, Yangkai Quan, Chuntao Zheng, Ling Huang, Kun Comput Struct Biotechnol J Review Article Lung cancer is one of the most common malignancies. In spite of the progress made in past decades, further studies to improve current therapy for lung cancer are required. Dynamically controlled by methyltransferases and demethylases, methylation of lysine and arginine residues on histone proteins regulates chromatin organization and thereby gene transcription. Aberrant alterations of histone methylation have been demonstrated to be associated with the progress of multiple cancers including lung cancer. Inhibitors of methyltransferases and demethylases have exhibited anti-tumor activities in lung cancer, and multiple lead candidates are under clinical trials. Here, we summarize how histone methylation functions in lung cancer, highlighting most recent progresses in small molecular inhibitors for lung cancer treatment. Research Network of Computational and Structural Biotechnology 2018-06-20 /pmc/articles/PMC6039709/ /pubmed/30002791 http://dx.doi.org/10.1016/j.csbj.2018.06.001 Text en © 2018 Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review Article
Chen, Yuchen
Liu, Xinran
Li, Yangkai
Quan, Chuntao
Zheng, Ling
Huang, Kun
Lung Cancer Therapy Targeting Histone Methylation: Opportunities and Challenges
title Lung Cancer Therapy Targeting Histone Methylation: Opportunities and Challenges
title_full Lung Cancer Therapy Targeting Histone Methylation: Opportunities and Challenges
title_fullStr Lung Cancer Therapy Targeting Histone Methylation: Opportunities and Challenges
title_full_unstemmed Lung Cancer Therapy Targeting Histone Methylation: Opportunities and Challenges
title_short Lung Cancer Therapy Targeting Histone Methylation: Opportunities and Challenges
title_sort lung cancer therapy targeting histone methylation: opportunities and challenges
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039709/
https://www.ncbi.nlm.nih.gov/pubmed/30002791
http://dx.doi.org/10.1016/j.csbj.2018.06.001
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