Essential Role of the 14q32 Encoded miRNAs in Endocrine Tumors

Genes (Basel). 2021 May 8;12(5):698. doi: 10.3390/genes12050698.

Abstract

Background: The 14q32 cluster is among the largest polycistronic miRNA clusters. miRNAs encoded here have been implicated in tumorigenesis of multiple organs including endocrine glands.

Methods: Critical review of miRNA studies performed in endocrine tumors have been performed. The potential relevance of 14q32 miRNAs through investigating their targets, and integrating the knowledge provided by literature data and bioinformatics predictions have been indicated.

Results: Pituitary adenoma, papillary thyroid cancer and a particular subset of pheochromocytoma and adrenocortical cancer are characterized by the downregulation of miRNAs encoded by the 14q32 cluster. Pancreas neuroendocrine tumors, most of the adrenocortical cancer and medullary thyroid cancer are particularly distinct, as 14q32 miRNAs were overexpressed. In pheochromocytoma and growth-hormone producing pituitary adenoma, however, both increased and decreased expression of 14q32 miRNAs cluster members were observed. In the background of this phenomenon methodological, technical and biological factors are hypothesized and discussed. The functions of 14q32 miRNAs were also revealed by bioinformatics and literature data mining.

Conclusions: 14q32 miRNAs have a significant role in the tumorigenesis of endocrine organs. Regarding their stable expression in the circulation of healthy individuals, further investigation of 14q32 miRNAs could provide a potential for use as biomarkers (diagnostic or prognostic) in endocrine neoplasms.

Keywords: 14q32; DLK1-MEG3 locus; adrenocortical cancer; endocrine tumor; miRNA; miRNA cluster; neuroendocrine tumor; pheochromocytoma; pituitary adenoma; thyroid cancer.

Publication types

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

MeSH terms

  • Chromosomes, Human, Pair 14 / genetics*
  • Endocrine Gland Neoplasms / genetics*
  • Endocrine Gland Neoplasms / metabolism
  • Gene Expression Regulation, Neoplastic
  • Genetic Loci
  • Humans
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism

Substances

  • MicroRNAs