Abstract
Background: N-acetylaspartate (NAA), the primary source of brain acetate, and aspartoacylase (ASPA), the enzyme that catabolizes NAA, are decreased in glioma, thereby decreasing acetate bioavailability. Results: Treatment with NAA and NAAG promotes growth and inhibits differentiation of glioma stem-like cells (GSCs). Conclusion: This study links acetate bioavailability and GSC malignancy. Significance: Because NAA/NAAG-mediated acetate supplementation promoted GSC growth, an alternative acetate therapeutic is required.
| Original language | English |
|---|---|
| Pages (from-to) | 26188-26200 |
| Number of pages | 13 |
| Journal | Journal of Biological Chemistry |
| Volume | 288 |
| Issue number | 36 |
| DOIs | |
| State | Published - 6 Sep 2013 |
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