Histone Demethylase Modulation: Epigenetic Strategy to Combat Cancer Progression

Author:

Srivastava Rashmi1ORCID,Singh Rubi2,Jauhari Shaurya3ORCID,Lodhi Niraj4ORCID,Srivastava Rakesh5ORCID

Affiliation:

1. Department of Zoology, Babasaheb Bhimrao Ambedkar University, Lucknow 226025, Uttar Pradesh, India

2. Department of Hematology, Bioreference Laboratories, Elmwood Park, NJ 07407, USA

3. Division of Education, Training, and Assessment, Global Education Center, Infosys Limited, Mysuru 570027, Karnataka, India

4. Clinical Research (Research and Development Division) Mirna Analytics LLC, Harlem Bio-Space, New York, NY 10027, USA

5. Molecular Biology and Microbiology, GenTox Research and Development, Lucknow 226001, Uttar Pradesh, India

Abstract

Epigenetic modifications are heritable, reversible changes in histones or the DNA that control gene functions, being exogenous to the genomic sequence itself. Human diseases, particularly cancer, are frequently connected to epigenetic dysregulations. One of them is histone methylation, which is a dynamically reversible and synchronously regulated process that orchestrates the three-dimensional epigenome, nuclear processes of transcription, DNA repair, cell cycle, and epigenetic functions, by adding or removing methylation groups to histones. Over the past few years, reversible histone methylation has become recognized as a crucial regulatory mechanism for the epigenome. With the development of numerous medications that target epigenetic regulators, epigenome-targeted therapy has been used in the treatment of malignancies and has shown meaningful therapeutic potential in preclinical and clinical trials. The present review focuses on the recent advances in our knowledge on the role of histone demethylases in tumor development and modulation, in emphasizing molecular mechanisms that control cancer cell progression. Finally, we emphasize current developments in the advent of new molecular inhibitors that target histone demethylases to regulate cancer progression.

Publisher

MDPI AG

Subject

Health, Toxicology and Mutagenesis,Genetics,Biochemistry, Genetics and Molecular Biology (miscellaneous),Biochemistry

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