The study reveals how drug-tolerant KRAS-mutant cancer cells adapt and how their metabolic vulnerabilities can be targeted (IMAGE)
Caption
The researchers found that drug-tolerant persister cells (DTPs) survive KRAS inhibition by reshaping their metabolism and becoming dependent on glutamine metabolism and lysosome-associated functions. Targeting these survival mechanisms reduces DTP survival under KRAS inhibition.
Credit
Dr. Shigeki Aoki from Chiba University, Japan Source link: https://doi.org/10.1038/s42003-026-10374-x
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