Chromatin Remodulator CHD4: A Potential Target for Cancer Interception

被引:0
|
作者
Goswami, Krishnendu [1 ]
Venkatachalam, Karthikkumar [1 ]
Singh, Surya P. [1 ]
Rao, Chinthalapally V. [1 ,2 ]
Madka, Venkateshwar [1 ]
机构
[1] Univ Oklahoma HSC, Ctr Canc Prevent & Drug Dev, Stephenson Canc Ctr, Dept Med,Hem Onc Sect, Oklahoma City, OK 73104 USA
[2] VA Med Ctr, Oklahoma City, OK 73104 USA
关键词
cancer; chromatin remodulation; chromosome; CHD4; epigenetics; nucleosome; PROTEIN; 4; CHD4; B-CELL DEVELOPMENT; REMODELER MI-2-BETA; GENE-EXPRESSION; STEM-CELLS; NURD; COMPLEX; PROGRESSION; REPAIR; ASSOCIATION;
D O I
10.3390/genes16020225
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cancer initiation and progression are associated with numerous somatic mutations, genomic rearrangements, and structure variants. The transformation of a normal cell into a cancer cell involves spatio-temporal changes in the regulation of different gene networks. The accessibility of these genes within the cell nucleus is manipulated via nucleosome remodeling ATPases, comprising one of the important mechanisms. Here, we reviewed studies of an ATP-dependent chromatin remodulator, chromodomain helicase DNA-binding 4 (CHD4), in cancer. Multiple domains of CHD4 are known to take part in nucleosome mobilization and histone binding. By binding with other proteins, CHD4 plays a vital role in transcriptional reprogramming and functions as a key component of Nucleosome Remodeling and Deacetylase, or NuRD, complexes. Here, we revisit data that demonstrate the role of CHD4 in cancer progression, tumor cell proliferation, DNA damage responses, and immune modulation. Conclusively, CHD4-mediated chromatin accessibility is essential for transcriptional reprogramming, which in turn is associated with tumor cell proliferation and cancer development.
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页数:18
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