TY - JOUR
T1 - mTOR Senses Intracellular pH through Lysosome Dispersion from RHEB
AU - Walton, Zandra E.
AU - Brooks, Rebekah C.
AU - Dang, Chi V.
N1 - Funding Information:
This work is partially supported by NCI grants R01CA051497 (C.V.D.), R01CA57341 (C.V.D.), F30CA200347 (Z.E.W.), T32CA9140‐39 (Z.E.W.), P30CA010815 (D. Altieri), the Patel Scholar Award (Z.E.W.), and the Ludwig Institute for Cancer Research.
Publisher Copyright:
© 2019 WILEY Periodicals, Inc.
PY - 2019/7
Y1 - 2019/7
N2 - Acidity, generated in hypoxia or hypermetabolic states, perturbs homeostasis and is a feature of solid tumors. That acid peripherally disperses lysosomes is a three-decade-old observation, yet one little understood or appreciated. However, recent work has recognized the inhibitory impact this spatial redistribution has on mechanistic target of rapamycin complex 1 (mTORC1), a key regulator of metabolism. This finding argues for a paradigm shift in localization of mTORC1 activator Ras homolog enriched in brain (RHEB), a conclusion several others have now independently reached. Thus, mTORC1, known to sense amino acids, mitogens, and energy to restrict biosynthesis to times of adequate resources, also senses pH and, via dampened mTOR-governed synthesis of clock proteins, regulates the circadian clock to achieve concerted responses to metabolic stress. While this may allow cancer to endure metabolic deprivation, immune cell mTOR signaling likewise exhibits pH sensitivity, suggesting that suppression of antitumor immune function by solid tumor acidity may additionally fuel cancers, an obstacle potentially reversible through therapeutic pH manipulation.
AB - Acidity, generated in hypoxia or hypermetabolic states, perturbs homeostasis and is a feature of solid tumors. That acid peripherally disperses lysosomes is a three-decade-old observation, yet one little understood or appreciated. However, recent work has recognized the inhibitory impact this spatial redistribution has on mechanistic target of rapamycin complex 1 (mTORC1), a key regulator of metabolism. This finding argues for a paradigm shift in localization of mTORC1 activator Ras homolog enriched in brain (RHEB), a conclusion several others have now independently reached. Thus, mTORC1, known to sense amino acids, mitogens, and energy to restrict biosynthesis to times of adequate resources, also senses pH and, via dampened mTOR-governed synthesis of clock proteins, regulates the circadian clock to achieve concerted responses to metabolic stress. While this may allow cancer to endure metabolic deprivation, immune cell mTOR signaling likewise exhibits pH sensitivity, suggesting that suppression of antitumor immune function by solid tumor acidity may additionally fuel cancers, an obstacle potentially reversible through therapeutic pH manipulation.
KW - Ras homolog enriched in brain (RHEB)
KW - acidity
KW - cancer immunity
KW - circadian clock
KW - lysosome trafficking
KW - mechanistic target of rapamycin (mTOR)
KW - pH
UR - http://www.scopus.com/inward/record.url?scp=85066979406&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85066979406&partnerID=8YFLogxK
U2 - 10.1002/bies.201800265
DO - 10.1002/bies.201800265
M3 - Article
C2 - 31157925
AN - SCOPUS:85066979406
SN - 0265-9247
VL - 41
JO - BioEssays
JF - BioEssays
IS - 7
M1 - 1800265
ER -