MicroRNAs in ER Stress: Divergent Roles in Cell Fate Decisions

Research output: Contribution to journalReview article

10 Citations (Scopus)

Abstract

MicroRNAs are small, noncoding RNAs which regulate protein expression post-transcriptionally. They respond to changes in a cell's environment and can promote cell death or cell survival depending on the context. Recent studies have linked microRNAs to the unfolded protein response pathway. This pathway is activated in the endoplasmic reticulum by conditions which interfere with the normal functions of the endoplasmic reticulum. The cell fate outcomes consequent to the activation of the unfolded protein response are binary, either cell survival or cell death. MicroRNAs can regulate multiple components of this pathway to tip the cell towards either fate. Inositol-requiring enzyme 1 alpha, a canonical unfolded protein response sensor and mediator, has inherent endoribonuclease activity. Interestingly, recently, it has been demonstrated that it can target microRNAs in addition to its previously known targets. This review highlights key papers in this rapidly emerging field.

Original languageEnglish (US)
Pages (from-to)117-122
Number of pages6
JournalCurrent Pathobiology Reports
Volume2
Issue number3
DOIs
StatePublished - Sep 1 2014
Externally publishedYes

Fingerprint

MicroRNAs
Unfolded Protein Response
Endoplasmic Reticulum
Cell Survival
Cell Death
Endoribonucleases
Small Untranslated RNA
Inositol
Enzymes
Proteins

Keywords

  • Activating transcription factor 4
  • Activating transcription factor 6 alpha
  • Apoptosis
  • C/EBP homologous protein
  • Inositol-requiring enzyme 1 alpha
  • Protein kinase-like ER kinase
  • Unfolded protein response

ASJC Scopus subject areas

  • Cell Biology
  • Molecular Biology
  • Pathology and Forensic Medicine
  • Cancer Research

Cite this

MicroRNAs in ER Stress : Divergent Roles in Cell Fate Decisions. / Malhi, Harmeet M.

In: Current Pathobiology Reports, Vol. 2, No. 3, 01.09.2014, p. 117-122.

Research output: Contribution to journalReview article

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