MicroRNAs in thyroid development, function and tumorigenesis

Mol Cell Endocrinol. 2017 Nov 15:456:44-50. doi: 10.1016/j.mce.2016.12.017. Epub 2016 Dec 21.

Abstract

MicroRNAs (miRNAs) are important post-transcriptional regulators of gene expression that modulate the vast majority of cellular processes. During development, the correct timing and expression of miRNAs in the tissue differentiation is essential for organogenesis and functionality. In thyroid gland, DICER and miRNAs are necessary for accurately establishing thyroid follicles and hormone synthesis. Moreover, DICER1 mutations and miRNA deregulation observed in human goiter influence thyroid tumorigenesis. The thyroid malignant transformation by MAPK oncogenes is accompanied by global miRNA changes, with a marked reduction of "tumor-suppressor" miRNAs and activation of oncogenic miRNAs. Loss of thyroid cell differentiation/function, and consequently iodine trapping impairment, is an important clinical characteristic of radioiodine-refractory thyroid cancer. However, few studies have addressed the direct role of miRNAs in thyroid gland physiology. Here, we focus on what we have learned in the thyroid follicular cell differentiation and function as revealed by cell and animal models and miRNA modulation in thyroid tumorigenesis.

Keywords: DICER; Iodine metabolism-related genes; MicroRNA; Thyroid; Thyroid cell differentiation; Thyroid tumor.

Publication types

  • Review

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / metabolism
  • Cell Transformation, Neoplastic / pathology
  • DEAD-box RNA Helicases / genetics*
  • DEAD-box RNA Helicases / metabolism
  • Gene Expression Regulation, Neoplastic*
  • Goiter / genetics*
  • Goiter / metabolism
  • Goiter / physiopathology
  • Humans
  • Iodine / metabolism
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Ribonuclease III / genetics*
  • Ribonuclease III / metabolism
  • Signal Transduction
  • Thyroid Epithelial Cells / metabolism
  • Thyroid Epithelial Cells / pathology
  • Thyroid Gland / metabolism*
  • Thyroid Gland / physiopathology
  • Thyroid Hormones / genetics
  • Thyroid Hormones / metabolism
  • Thyroid Neoplasms / genetics*
  • Thyroid Neoplasms / metabolism
  • Thyroid Neoplasms / physiopathology

Substances

  • MicroRNAs
  • Thyroid Hormones
  • Iodine
  • DICER1 protein, human
  • Ribonuclease III
  • DEAD-box RNA Helicases