Clinical implications of epigenetic regulation in oral cancer

Oral Oncol. 2015 Dec;51(12):1061-8. doi: 10.1016/j.oraloncology.2015.09.006. Epub 2015 Oct 5.

Abstract

Oral cancer is a high incidence cancer which is of major public health concern in India being the most common cancer in males and fifth most common cancer in females in India, contributing to 26% of the global oral cancer burden. The major risk factors of oral cancer are tobacco, alcohol and high risk Human Papilloma Virus type 16/18. However, only 3-12% of the high risk individuals with dysplasia develop oral cancer. Thus, individual genomic variants representing the genomic constitution and epigenetic alterations play a critical role in the development of oral cancer. Extensive epigenetic studies on the molecular lesions including oncogenes, tumor suppressor genes, genes associated with apoptosis, DNA damage repair have been reported. The current review highlights epigenetic regulation with a focus on molecular biomarkers and epidrug therapy in oral cancer. Epigenetic regulation by hypermethylation, histone modifications and specific microRNAs are often associated with early events and advanced stages in oral cancer, and thus indicate epidrug therapy for intervention. The presence of epigenetic marks in oral lesions, cancers and tumor associated mucosa emphasizes indications as biomarkers and epidrugs with therapeutic potential for better patient management.

Keywords: Biomarkers; DNA methylation; Epidrugs; Histone modifications; Oral cancer; microRNA.

Publication types

  • Review

MeSH terms

  • Apoptosis / genetics
  • Biomarkers, Tumor / genetics*
  • Cell Adhesion Molecules / genetics
  • DNA Repair / genetics
  • Epigenesis, Genetic*
  • Female
  • Genes, Tumor Suppressor
  • Genes, cdc / genetics
  • Histones / genetics
  • Humans
  • India
  • Male
  • MicroRNAs / genetics
  • Mouth Neoplasms / drug therapy
  • Mouth Neoplasms / genetics*
  • Wnt Signaling Pathway / genetics

Substances

  • Biomarkers, Tumor
  • Cell Adhesion Molecules
  • Histones
  • MicroRNAs