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Roles of Histone H2B, H3 and H4 Variants in Cancer Development and Prognosis

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

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Abstract

Histone variants are the paralogs of core histones (H2A, H2B, H3 and H4). They are stably expressed throughout the cell cycle in a replication-independent fashion and are capable of replacing canonical counterparts under different fundamental biological processes. Variants have been shown to take part in multiple processes, including DNA damage repair, transcriptional regulation and X chromosome inactivation, with some of them even specializing in lineage-specific roles like spermatogenesis. Several reports have recently identified some unprecedented variants from different histone families and exploited their prognostic value in distinct types of cancer. Among the four classes of canonical histones, the H2A family has the greatest number of variants known to date, followed by H2B, H3 and H4. In our prior review, we focused on summarizing all 19 mammalian histone H2A variants. Here in this review, we aim to complete the full summary of the roles of mammalian histone variants from the remaining histone H2B, H3, and H4 families, along with an overview of their roles in cancer biology and their prognostic value in a clinical context. © 2024 by the authors.
Original languageEnglish
Article number9699
JournalInternational Journal of Molecular Sciences
Volume25
Issue number17
Online published7 Sept 2024
DOIs
Publication statusPublished - Sept 2024

Funding

This work was supported by grants from the Research Grants Council of Hong Kong (Project No. 11105623 and 11104321) and the National Science Foundation of China (Project 8217111397) to K.M. Chan. Open Access made possible with partial support from the Open Access Publishing Fund of the City University of Hong Kong.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Research Keywords

  • cancers
  • chromatin
  • epigenetics
  • H2B
  • H3
  • H4
  • histone 2B variants
  • histone H3 variants
  • histone H4 variants
  • histone variants
  • variants

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

RGC Funding Information

  • RGC-funded

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