Article ID Journal Published Year Pages File Type
2039997 Cell Reports 2016 10 Pages PDF
Abstract

•ASS1-deficient tumors become resistant to arginine deprivation via ASS1 re-expression•ASS1-deficient cells have decreased levels of acetylated polyamine metabolites•Polyamine metabolites are decreased in ASS1-deficient cells upon arginine deprivation•ASS1 deficiency is synthetically lethal with inhibition of polyamine metabolism

SummaryArgininosuccinate synthase 1 (ASS1) is the rate-limiting enzyme for arginine biosynthesis. ASS1 expression is lost in a range of tumor types, including 50% of malignant pleural mesotheliomas. Starving ASS1-deficient cells of arginine with arginine blockers such as ADI-PEG20 can induce selective lethality and has shown great promise in the clinical setting. We have generated a model of ADI-PEG20 resistance in mesothelioma cells. This resistance is mediated through re-expression of ASS1 via demethylation of the ASS1 promoter. Through coordinated transcriptomic and metabolomic profiling, we have shown that ASS1-deficient cells have decreased levels of acetylated polyamine metabolites, together with a compensatory increase in the expression of polyamine biosynthetic enzymes. Upon arginine deprivation, polyamine metabolites are decreased in the ASS1-deficient cells and in plasma isolated from ASS1-deficient mesothelioma patients. We identify a synthetic lethal dependence between ASS1 deficiency and polyamine metabolism, which could potentially be exploited for the treatment of ASS1-negative cancers.

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