Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8408276 | Computational and Structural Biotechnology Journal | 2018 | 13 Pages |
Abstract
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.
Keywords
HDACPDXKLF2PRC2PTMsELK1Histone demethylationSAHPAD4TIMP3SAMS-adenosyl-l-homocysteineLSDsPRMTsPCNAMEP50methylosome protein 50S-adenosyl-L-methioninePatient-derived xenograftsALKProliferating Cell Nuclear AntigenImmunohistochemistryIHCSCLCposttranslational modificationsEMTLung cancerNSCLCSmall cell lung cancerNon-small cell lung cancerKruppel-like factor 2Anaplastic lymphoma kinaseTissue inhibitor of metalloproteinase 3Inhibitorshistone deacetylasehistone demethylaseHistone MethyltransferaseHistone methylationpolycomb repressive complex 2epithelial-to-mesenchymal transition
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Authors
Yuchen Chen, Xinran Liu, Yangkai Li, Chuntao Quan, Ling Zheng, Kun Huang,