Abstract
Summary:
Tumors mutated in IDH1 tend to have lower levels of the essential substrate NAD+. In this issue of Cancer Discovery, Nagashima and colleagues exploit this metabolic sensitivity by devising a combinatorial therapy that both further reduces the pools as well as sequesters the remaining substrate in PAR chains, sensitizing the cells to temozolomide and PARG inhibition.
See related article by Nagashima et al., p. 1672.
©2020 American Association for Cancer Research.
2020
American Association for Cancer Research.
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