| Literature DB >> 29396322 |
Ed Reznik1, Augustin Luna2, Bülent Arman Aksoy3, Eric Minwei Liu4, Konnor La5, Irina Ostrovnaya6, Chad J Creighton7, A Ari Hakimi8, Chris Sander9.
Abstract
Tumor metabolism is reorganized to support proliferation in the face of growth-related stress. Unlike the widespread profiling of changes to metabolic enzyme levels in cancer, comparatively less attention has been paid to the substrates/products of enzyme-catalyzed reactions, small-molecule metabolites. We developed an informatic pipeline to concurrently analyze metabolomics data from over 900 tissue samples spanning seven cancer types, revealing extensive heterogeneity in metabolic changes relative to normal tissue across cancers of different tissues of origin. Despite this heterogeneity, a number of metabolites were recurrently differentially abundant across many cancers, such as lactate and acyl-carnitine species. Through joint analysis of metabolomic data alongside clinical features of patient samples, we also identified a small number of metabolites, including several polyamines and kynurenine, which were associated with aggressive tumors across several tumor types. Our findings offer a glimpse onto common patterns of metabolic reprogramming across cancers, and the work serves as a large-scale resource accessible via a web application (http://www.sanderlab.org/pancanmet).Entities:
Keywords: cancer metabolism; clinical data; genomics; meta-analysis; metabolomics; tumor
Mesh:
Year: 2018 PMID: 29396322 PMCID: PMC5876114 DOI: 10.1016/j.cels.2017.12.014
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304