<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>35(24)</volume><submitter>van Geldermalsen M</submitter><pubmed_abstract>Alanine, serine, cysteine-preferring transporter 2 (ASCT2; SLC1A5) mediates uptake of glutamine, a conditionally essential amino acid in rapidly proliferating tumour cells. Uptake of glutamine and subsequent glutaminolysis is critical for activation of the mTORC1 nutrient-sensing pathway, which regulates cell growth and protein translation in cancer cells. This is of particular interest in breast cancer, as glutamine dependence is increased in high-risk breast cancer subtypes. Pharmacological inhibitors of ASCT2-mediated transport significantly reduced glutamine uptake in human breast cancer cell lines, leading to the suppression of mTORC1 signalling, cell growth and cell cycle progression. Notably, these effects were subtype-dependent, with ASCT2 transport critical only for triple-negativ</pubmed_abstract><journal>Oncogene</journal><pagination>3201-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4914826</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>ASCT2/SLC1A5 controls glutamine uptake and tumour growth in triple-negative basal-like breast cancer.</pubmed_title><pmcid>PMC4914826</pmcid><pubmed_authors>van Geldermalsen M</pubmed_authors><pubmed_authors>Ritchie W</pubmed_authors><pubmed_authors>Holst J</pubmed_authors><pubmed_authors>Rasko JE</pubmed_authors><pubmed_authors>Deng N</pubmed_authors><pubmed_authors>Feng Y</pubmed_authors><pubmed_authors>Nagarajah R</pubmed_authors><pubmed_authors>Beith JM</pubmed_authors><pubmed_authors>O'Toole SA</pubmed_authors><pubmed_authors>Gao D</pubmed_authors><pubmed_authors>Thoeng A</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Harvey K</pubmed_authors><pubmed_authors>Bailey CG</pubmed_authors><pubmed_authors>Marshall AD</pubmed_authors><pubmed_authors>Selinger CI</pubmed_authors></additional><is_claimable>false</is_claimable><name>ASCT2/SLC1A5 controls glutamine uptake and tumour growth in triple-negative basal-like breast cancer.</name><description>Alanine, serine, cysteine-preferring transporter 2 (ASCT2; SLC1A5) mediates uptake of glutamine, a conditionally essential amino acid in rapidly proliferating tumour cells. Uptake of glutamine and subsequent glutaminolysis is critical for activation of the mTORC1 nutrient-sensing pathway, which regulates cell growth and protein translation in cancer cells. This is of particular interest in breast cancer, as glutamine dependence is increased in high-risk breast cancer subtypes. Pharmacological inhibitors of ASCT2-mediated transport significantly reduced glutamine uptake in human breast cancer cell lines, leading to the suppression of mTORC1 signalling, cell growth and cell cycle progression. Notably, these effects were subtype-dependent, with ASCT2 transport critical only for triple-negativ</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jun</publication><modification>2026-05-05T14:47:19.584Z</modification><creation>2019-03-27T02:16:34Z</creation></dates><accession>S-EPMC4914826</accession><cross_references><pubmed>26455325</pubmed><doi>10.1038/onc.2015.381</doi></cross_references></HashMap>