Lung Cancer Therapy Targeting Histone Methylation: Opportunities and Challenges

被引:48
作者
Chen, Yuchen [1 ]
Liu, Xinran [1 ]
Li, Yangkai [2 ]
Quan, Chuntao [1 ]
Zheng, Ling [3 ]
Huang, Kun [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Sch Pharm, Tongji Med Coll, Wuhan 430030, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Wuhan 430030, Hubei, Peoples R China
[3] Wuhan Univ, Coll Life Sci, Wuhan 430072, Peoples R China
关键词
Histone methylation; Histone demethylation; Lung cancer; Histone methyltransferase; Histone demethylase; Inhibitors; H3K27 DEMETHYLASE INHIBITOR; BREAST-CANCER; SET DOMAIN; LYSINE METHYLTRANSFERASES; LSD1; INHIBITORS; MESENCHYMAL TRANSITION; PERSONALIZED TREATMENT; EPIGENETIC REGULATORS; ARGININE METHYLATION; MOLECULAR-MECHANISMS;
D O I
10.1016/j.csbj.2018.06.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (c) 2018 Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:211 / 223
页数:13
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