Phenotype-based cell-specific metabolic modeling reveals metabolic liabilities of cancer
2014; eLife Sciences Publications Ltd; Volume: 3; Linguagem: Inglês
10.7554/elife.03641
ISSN2050-084X
AutoresKeren Yizhak, Edoardo Gaude, Sylvia E. Le Dévédec, Yedael Y. Waldman, Gideon Y. Stein, Bob van de Water, Christian Frezza, Eytan Ruppin,
Tópico(s)Gene Regulatory Network Analysis
ResumoUtilizing molecular data to derive functional physiological models tailored for specific cancer cells can facilitate the use of individually tailored therapies. To this end we present an approach termed PRIME for generating cell-specific genome-scale metabolic models (GSMMs) based on molecular and phenotypic data. We build >280 models of normal and cancer cell-lines that successfully predict metabolic phenotypes in an individual manner. We utilize this set of cell-specific models to predict drug targets that selectively inhibit cancerous but not normal cell proliferation. The top predicted target, MLYCD, is experimentally validated and the metabolic effects of MLYCD depletion investigated. Furthermore, we tested cell-specific predicted responses to the inhibition of metabolic enzymes, and successfully inferred the prognosis of cancer patients based on their PRIME-derived individual GSMMs. These results lay a computational basis and a counterpart experimental proof of concept for future personalized metabolic modeling applications, enhancing the search for novel selective anticancer therapies.
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