TY - JOUR
T1 - SNAT7 regulates mTORC1 via macropinocytosis
AU - Meng, Delong
AU - Yang, Qianmei
AU - Jeong, Mi Hyeon
AU - Curukovic, Adna
AU - Tiwary, Shweta
AU - Melick, Chase H.
AU - Lama-Sherpa, Tshering D.
AU - Wang, Huanyu
AU - Huerta-Rosario, Mariela
AU - Urquhart, Greg
AU - Zacharias, Lauren G.
AU - Lewis, Cheryl
AU - DeBerardinis, Ralph J.
AU - Jewell, Jenna L.
PY - 2022/5/17
Y1 - 2022/5/17
N2 - SignificanceThe mammalian target of rapamycin complex 1 (mTORC1) signaling pathway is frequently elevated in human disease, including cancer, type 2 diabetes, metabolic disorders, and neurodegeneration. We identify SNAT7 as an important regulator of mTORC1. We believe this research will provide valuable insight about mTORC1 biology and may uncover novel therapeutic targets for patients.
AB - SignificanceThe mammalian target of rapamycin complex 1 (mTORC1) signaling pathway is frequently elevated in human disease, including cancer, type 2 diabetes, metabolic disorders, and neurodegeneration. We identify SNAT7 as an important regulator of mTORC1. We believe this research will provide valuable insight about mTORC1 biology and may uncover novel therapeutic targets for patients.
KW - macropinocytosis
KW - mTOR
KW - SNAT7
UR - http://www.scopus.com/inward/record.url?scp=85130072505&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85130072505&partnerID=8YFLogxK
U2 - 10.1073/pnas.2123261119
DO - 10.1073/pnas.2123261119
M3 - Article
C2 - 35561222
AN - SCOPUS:85130072505
VL - 119
SP - e2123261119
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
SN - 0027-8424
IS - 20
ER -