Epigenetic regulation of RET receptor tyrosine kinase and non-coding RNAs in MTC

Mol Cell Endocrinol. 2018 Jul 5:469:48-53. doi: 10.1016/j.mce.2017.03.014. Epub 2017 Mar 15.

Abstract

Medullary thyroid carcinoma (MTC) is an aggressive and rare cancer with limited treatment options for metastatic disease. Due to this, there is a need for a better understanding of MTC biology in the hope of improved treatments. One area of improved understanding of cancer biology is epigenetics. Epigenetics is defined as cellular processes which alter gene expression independent of changes in the primary DNA sequence. These processes include modifications such as DNA methylation, microRNA deregulation and post-translational histone modifications, all of which have been implicated in tumorigenesis of MTC. Transcription of the main driver of MTC - the REarranged during Transfection (RET) proto-oncogene can also be modulated by epigenetic alterations. This review will present a review of MTC and its epigenetic links with a particular focus on targeting epigenetic mechanisms as novel therapeutic strategies.

Keywords: Epigenetics; Medullary thyroid carcinoma; MicroRNA; Noncoding RNA; RET.

Publication types

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

MeSH terms

  • Animals
  • Carcinoma, Neuroendocrine / genetics*
  • Carcinoma, Neuroendocrine / pathology
  • DNA Methylation / genetics
  • Epigenesis, Genetic*
  • Humans
  • Molecular Targeted Therapy
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins c-ret / genetics*
  • Proto-Oncogene Proteins c-ret / metabolism
  • RNA, Untranslated / genetics*
  • RNA, Untranslated / metabolism
  • Thyroid Neoplasms / genetics*
  • Thyroid Neoplasms / pathology

Substances

  • MAS1 protein, human
  • Proto-Oncogene Mas
  • RNA, Untranslated
  • Proto-Oncogene Proteins c-ret

Supplementary concepts

  • Thyroid cancer, medullary