| Literature DB >> 34649481 |
Debanjan Bhattacharya1, Vaibhavkumar S Gawali1, Laura Kallay1, Donatien K Toukam1, Abigail Koehler1, Peter Stambrook1, Daniel Pomeranz Krummel1, Soma Sengupta1.
Abstract
γ-aminobutyric acid or GABA is an amino acid that functionally acts as a neurotransmitter and is critical to neurotransmission. GABA is also a metabolite in the Krebs cycle. It is therefore unsurprising that GABA and its receptors are also present outside of the central nervous system, including in immune cells. This observation suggests that GABAergic signaling impacts events beyond brain function and possibly human health beyond neurological disorders. Indeed, GABA receptor subunits are expressed in pathological disease states, including in disparate cancers. The role that GABA and its receptors may play in cancer development and progression remains unclear. If, however, those cancers have functional GABA receptors that participate in GABAergic signaling, it raises an important question whether these signaling pathways might be targetable for therapeutic benefit. Herein we summarize the effects of modulating Type-A GABA receptor signaling in various cancers and highlight how Type-A GABA receptors could emerge as a novel therapeutic target in cancer.Entities:
Keywords: GABA; GABAA receptors; benzodiazepines; cancer; ion channels
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Year: 2021 PMID: 34649481 PMCID: PMC8524771 DOI: 10.1177/15353702211032549
Source DB: PubMed Journal: Exp Biol Med (Maywood) ISSN: 1535-3699