» Articles » PMID: 26590715

Drugging Chromatin in Cancer: Recent Advances and Novel Approaches

Overview
Journal Mol Cell
Publisher Cell Press
Specialty Cell Biology
Date 2015 Nov 23
PMID 26590715
Citations 31
Authors
Affiliations
Soon will be listed here.
Abstract

Chromatin regulatory mechanisms play a major role in the control of gene expression programs during normal development and are disrupted in specific disease states, particularly in cancer. Important mediators of chromatin regulatory processes can broadly be classified into writers, erasers, and readers of covalent chromatin modifications that modulate eukaryotic gene transcription and maintain the integrity of the genome. The reversibility and disease-specific nature of these chromatin states make these regulators attractive therapeutic targets. As such, there is an ever-increasing number of candidate therapies aimed at targeting cancer-associated chromatin states that are in various stages of preclinical and clinical development. In this review, we discuss recent advances that have been made in the rational therapeutic targeting of chromatin regulatory mechanisms and highlight certain cancers where there is a specific rationale to assess these therapeutic approaches.

Citing Articles

Pan-cancer landscape of epigenetic factor expression predicts tumor outcome.

Cheng M, Mitra M, Coller H Commun Biol. 2023; 6(1):1138.

PMID: 37973839 PMC: 10654613. DOI: 10.1038/s42003-023-05459-w.


DNA mimic foldamers affect chromatin composition and disturb cell cycle progression.

Kleene V, Corvaglia V, Chacin E, Forne I, Konrad D, Khosravani P Nucleic Acids Res. 2023; 51(18):9629-9642.

PMID: 37650653 PMC: 10570015. DOI: 10.1093/nar/gkad681.


The histone chaperone FACT: a guardian of chromatin structure integrity.

Jeronimo C, Robert F Transcription. 2022; 13(1-3):16-38.

PMID: 35485711 PMC: 9467567. DOI: 10.1080/21541264.2022.2069995.


DNA folds threaten genetic stability and can be leveraged for chemotherapy.

Zell J, Rota Sperti F, Britton S, Monchaud D RSC Chem Biol. 2022; 2(1):47-76.

PMID: 35340894 PMC: 8885165. DOI: 10.1039/d0cb00151a.


Comprehensive Comparative Molecular Characterization of Young and Old Lung Cancer Patients.

Hu M, Tan J, Liu Z, Li L, Zhang H, Zhao D Front Oncol. 2022; 11:806845.

PMID: 35096611 PMC: 8789686. DOI: 10.3389/fonc.2021.806845.


References
1.
Deshpande A, Bradner J, Armstrong S . Chromatin modifications as therapeutic targets in MLL-rearranged leukemia. Trends Immunol. 2012; 33(11):563-70. PMC: 4034385. DOI: 10.1016/j.it.2012.06.002. View

2.
Kadoch C, Hargreaves D, Hodges C, Elias L, Ho L, Ranish J . Proteomic and bioinformatic analysis of mammalian SWI/SNF complexes identifies extensive roles in human malignancy. Nat Genet. 2013; 45(6):592-601. PMC: 3667980. DOI: 10.1038/ng.2628. View

3.
Falkenberg K, Johnstone R . Histone deacetylases and their inhibitors in cancer, neurological diseases and immune disorders. Nat Rev Drug Discov. 2014; 13(9):673-91. DOI: 10.1038/nrd4360. View

4.
Lv T, Yuan D, Miao X, Lv Y, Zhan P, Shen X . Over-expression of LSD1 promotes proliferation, migration and invasion in non-small cell lung cancer. PLoS One. 2012; 7(4):e35065. PMC: 3320866. DOI: 10.1371/journal.pone.0035065. View

5.
Pasqualucci L, Dominguez-Sola D, Chiarenza A, Fabbri G, Grunn A, Trifonov V . Inactivating mutations of acetyltransferase genes in B-cell lymphoma. Nature. 2011; 471(7337):189-95. PMC: 3271441. DOI: 10.1038/nature09730. View