Abstract
The kinase mammalian target of rapamycin (mTOR) is a major regulatory hub that senses and integrates nutrient, energy, and growth factor inputs to promote cell growth. In this issue of EMBO Reports, Byun et al [1] report that high intracellular levels of lactate activate mTORC1 in KRAS transformed cells independently of a growth factor input. This suggests a mechanism for how mTORC1 can be co‐opted to support oncogenic growth and proliferation.
MeSH terms
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Cytoplasm
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Lactic Acid*
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Mechanistic Target of Rapamycin Complex 1
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Proto-Oncogene Proteins p21(ras)*
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Signal Transduction
Substances
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Lactic Acid
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Mechanistic Target of Rapamycin Complex 1
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Proto-Oncogene Proteins p21(ras)