Why the study?
Lack of specific Hv1 inhibitors has hampered translation of knowledge about Hv1's role in immune, fertility, and malignancy diseases to therapeutic applications.
The discovery of novel Hv1 inhibitors and the demonstration that Hv1 deletion delays tumor development suggest a new therapeutic target for cancer.
Answers are grounded in this paper and cite their sources.
Hv1 emerges as a potential target in granulocytic sarcoma; leaves open whether novel inhibitors will prove effective in humans.
The voltage-gated hydrogen channel Hv1 encoded in humans by the HVCN1 gene is a highly selective proton channel that allows large fluxes of protons across biological membranes. Hv1 form functional dimers of four transmembrane spanning proteins resembling the voltage sensing domain of potassium channels. Each subunit is highly selective for protons and is controlled by changes in the transmembrane voltage and pH gradient. Hv1 is most expressed in phagocytic cells where it sustains NADPH oxidase-dependent bactericidal function and was reported to facilitate antibody production by B cells and to promote the maturation and motility of spermatocytes. Hv1 contributes to neuroinflammation following brain damage and favors cancer progression possibly by extruding protons generated during aerobic glycolysis of cancer cells. Lack of specific Hv1 inhibitors has hampered translation of this knowledge to treat immune, fertility, or malignancy diseases. In this study, we show that the genetic deletion of Hv1 delays tumor development in a mouse model of granulocytic sarcoma and report the discovery and characterization of two novel bioavailable inhibitors of Hv1 channels that we validate by orthogonal assays and electrophysiological recordings.
No takes yet. Share an insight, caveat, or question.
Chemaly et al. (2023) studied Granulocytic sarcoma (n=20). Genetic deletion of Hv1 vs. Wild-type PLB-985 cells was evaluated on Tumor volume at day 22 (p=<0.05).
Synapse has enriched 10 related papers. Consider them for comparative context: