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The landscape of cancer cell line metabolism

Authors :
David E. Root
Clary B. Clish
Mahmoud Ghandi
William R. Sellers
Verena Apfel
Kerry A. Pierce
William C. Hahn
Shuba Gopal
Raymond Pagliarini
Dojna Shkoza
Shaoyang Ning
Francisca Vazquez
Aviad Tsherniak
Levi A. Garraway
Stuart L. Schreiber
Amanda Souza
Amy Deik
Yilong Zou
Marios Giannakis
Gregory V. Kryukov
Julie Ann
Paula Keskula
Giorgio G. Galli
Haoxin Li
Desiree Hernandez
Jordi Barretina
Source :
Nature Medicine. 25:850-860
Publication Year :
2019
Publisher :
Springer Science and Business Media LLC, 2019.

Abstract

Despite considerable efforts to identify cancer metabolic alterations that might unveil druggable vulnerabilities, systematic characterizations of metabolism as it relates to functional genomic features and associated dependencies remain uncommon. To further understand the metabolic diversity of cancer, we profiled 225 metabolites in 928 cell lines from more than 20 cancer types in the Cancer Cell Line Encyclopedia (CCLE) using liquid chromatography–mass spectrometry (LC-MS). This resource enables unbiased association analysis linking the cancer metabolome to genetic alterations, epigenetic features and gene dependencies. Additionally, by screening barcoded cell lines, we demonstrated that aberrant ASNS hypermethylation sensitizes subsets of gastric and hepatic cancers to asparaginase therapy. Finally, our analysis revealed distinct synthesis and secretion patterns of kynurenine, an immune-suppressive metabolite, in model cancer cell lines. Together, these findings and related methodology provide comprehensive resources that will help clarify the landscape of cancer metabolism. Systematic metabolite profiling across cancer cell lines uncovers patterns associated with genetic and epigenetic features and reveals dysregulated metabolic states that can be exploited for anticancer therapy

Details

ISSN :
1546170X and 10788956
Volume :
25
Database :
OpenAIRE
Journal :
Nature Medicine
Accession number :
edsair.doi.dedup.....980f500fd90efe8bb919bee7bfe0bea3
Full Text :
https://doi.org/10.1038/s41591-019-0404-8