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Histone demethylases in prostate cancer

  • Ling Yu Wang
  • , Wenchang Guo
  • , Kevin Kim
  • , Mamata Pochampalli
  • , Chiu Lien Hung
  • , Yoshihiro Izumiya
  • , Hsing Jien Kung*
  • *Corresponding author for this work
  • University of California at Davis

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

2 Scopus citations

Abstract

Accumulating evidence has suggested that epigenetic alternations are as important as genetic mutations in cancer development. It is proposed that tumors are arisen by "malignant reprogramming" driven by a combination of both genetic and epigenetic changes. It therefore comes as no surprise that histone demethylases, the newest members of the histone modifying enzymes, are found to be targets of mutations and dysregulation in cancer cells. In this review article, we provide an overview of the types of histone demethylases whose genetic structure or expression is altered in cancers, the action of histone demethylases in cancer development and their potential inhibitors. Special emphasis is placed on the roles of histone demethylases in prostate cancer progression.

Original languageEnglish
Title of host publicationNuclear Signaling Pathways and Targeting Transcription in Cancer
PublisherHumana Press Inc.
Pages373-397
Number of pages25
ISBN (Print)9781461480389
DOIs
StatePublished - 2014
Externally publishedYes

Publication series

NameCancer Drug Discovery and Development
Volume88
ISSN (Print)2196-9906
ISSN (Electronic)2196-9914

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

Keywords

  • Epigenetics
  • Histone demethylase
  • Inhibitor
  • Mutation
  • Prostate cancer

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