4.7 Review

MicroRNAs as Regulators of Cancer Cell Energy Metabolism

Journal

JOURNAL OF PERSONALIZED MEDICINE
Volume 12, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/jpm12081329

Keywords

miRNA; cancer metabolism; TCA; glucose oxidation; pentose-phosphate pathway; fatty acid oxidation

Funding

  1. W.W.Smith Charitable Trust [H2103]
  2. American Heart Association [935207]
  3. NIH [R00 HL138268, R21DA051798]
  4. Penn State College of Medicine

Ask authors/readers for more resources

Cancer cells rapidly reprogram their metabolism to adapt to the tumor environment or escape chemotherapy. Recent studies have shown that cancer cells rely on glutamine, lipid, and mitochondrial metabolism for energy. Some miRNAs play a key role in regulating these metabolic changes. Additionally, miRNAs can regulate mitochondrial calcium stores and energy metabolism, promoting cancer cell survival, growth, and metastasis.
To adapt to the tumor environment or to escape chemotherapy, cancer cells rapidly reprogram their metabolism. The hallmark biochemical phenotype of cancer cells is the shift in metabolic reprogramming towards aerobic glycolysis. It was thought that this metabolic shift to glycolysis alone was sufficient for cancer cells to meet their heightened energy and metabolic demands for proliferation and survival. Recent studies, however, show that cancer cells rely on glutamine, lipid, and mitochondrial metabolism for energy. Oncogenes and scavenging pathways control many of these metabolic changes, and several metabolic and tumorigenic pathways are post-transcriptionally regulated by microRNA (miRNAs). Genes that are directly or indirectly responsible for energy production in cells are either negatively or positively regulated by miRNAs. Therefore, some miRNAs play an oncogenic role by regulating the metabolic shift that occurs in cancer cells. Additionally, miRNAs can regulate mitochondrial calcium stores and energy metabolism, thus promoting cancer cell survival, cell growth, and metastasis. In the electron transport chain (ETC), miRNAs enhance the activity of apoptosis-inducing factor (AIF) and cytochrome c, and these apoptosome proteins are directed towards the ETC rather than to the apoptotic pathway. This review will highlight how miRNAs regulate the enzymes, signaling pathways, and transcription factors of cancer cell metabolism and mitochondrial calcium import/export pathways. The review will also focus on the metabolic reprogramming of cancer cells to promote survival, proliferation, growth, and metastasis with an emphasis on the therapeutic potential of miRNAs for cancer treatment.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available