Role of MTA1 in head and neck cancers

Cancer Metastasis Rev. 2014 Dec;33(4):953-64. doi: 10.1007/s10555-014-9521-5.

Abstract

Head and neck cancers usually originate in the squamous cells that line the inner mucosal surfaces of the oral and the neck region. These cancers follow multifocal steps for progression that include risk of developing metastasis. Although therapeutics has advanced in the past decades, head and neck cancers continue to cause much morbidity and mortality. Even with the promising effect of targeted therapies, there is a need for a better evaluation of patients with head and neck cancers. Metastasis-associated tumour antigen 1 (MTA1), a chromatin modifier, is found as an integral part of nucleosome remodelling and histone deacetylation (NuRD) complex. MTA1 is a biomarker for several solid tumours, and the overexpression of which have been documented in various cancers such as breast, ovarian, colon, prostrate etc. Interestingly also, a set of head and neck cancers shows MTA1 overexpression. However, recent evidences from clinical data raise a critical question on the role of MTA1 in head and neck cancers. This calls for a detailed review to the role of MTA1 in oral cancer. This review gives a brief account on the existing biological and molecular data in the context of head and neck cancer invasion and metastasis in relation to MTA1.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Biomarkers, Tumor / genetics*
  • Gene Expression Regulation, Neoplastic
  • Head and Neck Neoplasms / genetics*
  • Head and Neck Neoplasms / pathology
  • Histone Deacetylases / biosynthesis
  • Histone Deacetylases / genetics*
  • Humans
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex / genetics
  • Neoplasm Invasiveness / genetics
  • Neoplasm Metastasis / genetics
  • Repressor Proteins / biosynthesis
  • Repressor Proteins / genetics*
  • Trans-Activators

Substances

  • Biomarkers, Tumor
  • MTA1 protein, human
  • Repressor Proteins
  • Trans-Activators
  • Histone Deacetylases
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex