4.5 Review

Molecular Mechanisms of Oncogenesis through the Lens of Nucleosomes and Histones

Journal

JOURNAL OF PHYSICAL CHEMISTRY B
Volume 125, Issue 16, Pages 3963-3976

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.1c00694

Keywords

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Funding

  1. Department of Pathology and Molecular Medicine, Queen's University, Canada
  2. Senior Canada Research Chair in Computational Biology and Biophysics
  3. Ontario Institute of Cancer Research, Canada
  4. Russian Science Foundation [18-74-10006]
  5. Russian Foundation for Basic Research [19-34-51053]
  6. Interdisciplinary Scientific and Educational School of Moscow University Molecular Technologies of the Living Systems and Synthetic Biology
  7. Russian Science Foundation [18-74-10006] Funding Source: Russian Science Foundation

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Cancer involves the interplay between the genome and epigenome at the cellular level, with nucleosomes playing a crucial role. Mutations, changes in expression, and slicing of histones can affect epigenetic dysregulation and carcinogenesis. The differential expression of histone variants and isoforms is linked to cancer phenotypes.
At the cellular level, cancer is the disease of both the genome and the epigenome, and the interplay between genetic mutations and epigenetic states may occur at the level of elementary chromatin units, the nucleosomes. They are formed by a segment of DNA wrapped around an octamer of histone proteins. In this review, we survey various mechanisms of cancer etiology and progression mediated by histones and nucleosomes. In particular, we discuss the effects of mutations in histones, changes in their expression and slicing on epigenetic dysregulation and carcinogenesis. The links between cancer phenotypes and differential expression of histone variants and isoforms are summarized. Finally, we discourse the geometric and steric effects of DNA compaction in nucleosomes on DNA mutation rate, interactions with transcription factors, including pioneer transcription factors, and prospects of cancer cells' genome and epigenome editing.

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