{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["8(1)"],"submitter":["Filippakis H"],"pubmed_abstract":["Tuberous Sclerosis Complex (TSC), a rare genetic disorder with mechanistic target of rapamycin complex 1 (mTORC1) hyperactivation, is characterized by multi-organ hamartomatous benign tumors including brain, skin, kidney, and lung (Lymphangioleiomyomatosis). mTORC1 hyperactivation drives metabolic reprogramming including glucose and glutamine utilization, protein, nucleic acid and lipid synthesis. To investigate the mechanisms of exogenous nutrients uptake in Tsc2-deficient cells, we measured dextran uptake, a polysaccharide internalized via macropinocytosis. Tsc2-deficient cells showed a striking increase in dextran uptake (3-fold, p < 0.0001) relative to Tsc2-expressing cells, which was decreased (3-fold, p < 0.0001) with mTOR inhibitor, Torin1. Pharmacologic and genetic inhibition of th"],"journal":["Scientific reports"],"pagination":["14161"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6155086"],"repository":["biostudies-literature"],"pubmed_title":["Vps34-mediated macropinocytosis in Tuberous Sclerosis Complex 2-deficient cells supports tumorigenesis."],"pmcid":["PMC6155086"],"pubmed_authors":["Nijmeh J","Belaid A","Hougard T","Siroky B","Wu C","Filippakis H","Lam HC","Alesi N","Henske EP"],"additional_accession":[]},"is_claimable":false,"name":"Vps34-mediated macropinocytosis in Tuberous Sclerosis Complex 2-deficient cells supports tumorigenesis.","description":"Tuberous Sclerosis Complex (TSC), a rare genetic disorder with mechanistic target of rapamycin complex 1 (mTORC1) hyperactivation, is characterized by multi-organ hamartomatous benign tumors including brain, skin, kidney, and lung (Lymphangioleiomyomatosis). mTORC1 hyperactivation drives metabolic reprogramming including glucose and glutamine utilization, protein, nucleic acid and lipid synthesis. To investigate the mechanisms of exogenous nutrients uptake in Tsc2-deficient cells, we measured dextran uptake, a polysaccharide internalized via macropinocytosis. Tsc2-deficient cells showed a striking increase in dextran uptake (3-fold, p < 0.0001) relative to Tsc2-expressing cells, which was decreased (3-fold, p < 0.0001) with mTOR inhibitor, Torin1. Pharmacologic and genetic inhibition of th","dates":{"release":"2018-01-01T00:00:00Z","publication":"2018 Sep","modification":"2026-06-07T06:33:21.297Z","creation":"2019-03-26T23:57:40Z"},"accession":"S-EPMC6155086","cross_references":{"pubmed":["30242175"],"doi":["10.1038/s41598-018-32256-x"]}}