HMGA1-pseudogenes and cancer

Oncotarget. 2016 May 10;7(19):28724-35. doi: 10.18632/oncotarget.7427.

Abstract

Pseudogenes are DNA sequences with high homology to the corresponding functional gene, but, because of the accumulation of various mutations, they have lost their initial functions to code for proteins. Consequently, pseudogenes have been considered until few years ago dysfunctional relatives of the corresponding ancestral genes, and then useless in the course of genome evolution. However, several studies have recently established that pseudogenes are owners of key biological functions. Indeed, some pseudogenes control the expression of functional genes by competitively binding to the miRNAs, some of them generate small interference RNAs to negatively modulate the expression of functional genes, and some of them even encode functional mutated proteins. Here, we concentrate our attention on the pseudogenes of the HMGA1 gene, that codes for the HMGA1a and HMGA1b proteins having a critical role in development and cancer progression. In this review, we analyze the family of HMGA1 pseudogenes through three aspects: classification, characterization, and their possible function and involvement in cancer.

Keywords: HMGA; cancer; ceRNA; pseudogenes.

Publication types

  • Review

MeSH terms

  • Disease Progression
  • Gene Expression Regulation, Neoplastic
  • HMGA1a Protein / genetics*
  • HMGA1a Protein / metabolism
  • HMGA1b Protein / genetics*
  • HMGA1b Protein / metabolism
  • Humans
  • Models, Genetic
  • Mutation
  • Neoplasms / genetics*
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Pseudogenes / genetics*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism

Substances

  • RNA, Messenger
  • HMGA1b Protein
  • HMGA1a Protein