Abstract
Oligodendroglioma is characterized by mutations of IDH and CIC, 1p/19q loss, and slow growth. We found that NHE-1 on 1p is silenced in oligodendrogliomas secondary to IDH-associated hypermethylation and 1p allelic loss. Silencing lowers intracellular pH and attenuates acid load recovery in oligodendroglioma cells. Others have shown that rapid tumor growth cannot occur without NHE-1-mediated neutralization of the acidosis generated by the Warburg glycolytic shift. Our findings show for the first time that the pH regulator NHE-1 can be silenced in a human cancer and also suggest that pH deregulation may contribute to the distinctive biology of human oligodendroglioma. © 2012 American Neurological Association.
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CITATION STYLE
Blough, M. D., Al-Najjar, M., Chesnelong, C., Binding, C. E., Rogers, A. D., Luchman, H. A., … Gregory Cairncross, J. (2012). DNA hypermethylation and 1p loss silence NHE-1 in oligodendroglioma. Annals of Neurology, 71(6), 845–849. https://doi.org/10.1002/ana.23610
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