HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The pivotal role of MicroRNAs in glucose metabolism in cancer.

Abstract
Cancer cells are able to undergo aerobic glycolysis and metabolize glucose to lactate instead of oxidative phosphorylation, which is known as Warburg effect. Accumulating evidence has revealed that microRNAs regulate cancer cell metabolism, which manifest a higher rate of glucose metabolism. Various signaling pathways along with glycolytic enzymes are responsible for the emergence of glycolytic dependence. MicroRNAs are a class of non-coding RNAs that are not translated into proteins but regulate target gene expression or in other words function pre-translationally and post-transcriptionally. MicroRNAs have been shown to be involved in various biological processes, including glucose metabolism via targeting major transcription factors, enzymes, oncogenes or tumor suppressors alongside the oncogenic signaling pathways. In this review, we describe the regulatory role of microRNAs of cancer cell glucose metabolism, including in the glucose uptake, glycolysis, tricarboxylic acid cycle and several signaling pathways and further suggest that microRNA-based therapeutics can be used to inhibit the process of glucose metabolism reprogramming in cancer cells and thus suppressing cancer progression.
AuthorsSina Taefehshokr, Nima Taefehshokr, Nima Hemmat, Saba Hajazimian, Alireza Isazadeh, Pourya Dadebighlu, Behzad Baradaran
JournalPathology, research and practice (Pathol Res Pract) Vol. 217 Pg. 153314 (Jan 2021) ISSN: 1618-0631 [Electronic] Germany
PMID33341548 (Publication Type: Journal Article, Review)
CopyrightCopyright © 2020 Elsevier GmbH. All rights reserved.
Chemical References
  • MicroRNAs
  • MTOR protein, human
  • Phosphatidylinositol 3-Kinase
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases
  • Glucose
Topics
  • Animals
  • Energy Metabolism
  • Gene Expression Regulation, Neoplastic
  • Glucose (metabolism)
  • Humans
  • MicroRNAs (genetics, metabolism)
  • Neoplasms (genetics, metabolism, pathology)
  • Phosphatidylinositol 3-Kinase (metabolism)
  • Proto-Oncogene Proteins c-akt (metabolism)
  • Signal Transduction
  • TOR Serine-Threonine Kinases (metabolism)
  • Warburg Effect, Oncologic

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: