| Literature DB >> 30759381 |
Irena Roci1, Jeramie D Watrous2, Kim A Lagerborg2, Lorenzo Lafranchi3, Arne Lindqvist3, Mohit Jain2, Roland Nilsson4.
Abstract
Alterations in cell-cycle regulation and cellular metabolism are associated with cancer transformation, and enzymes active in the committed cell-cycle phase may represent vulnerabilities of cancer cells. Here, we map metabolic events in the G1 and SG2M phases by combining cell sorting with mass spectrometry-based isotope tracing, revealing hundreds of cell-cycle-associated metabolites. In particular, arginine uptake and ornithine synthesis are active during SG2M in transformed but not in normal cells, with the mitochondrial arginase 2 (ARG2) enzyme as a potential mechanism. While cancer cells exclusively use ARG2, normal epithelial cells synthesize ornithine via ornithine aminotransferase (OAT). Knockdown of ARG2 markedly reduces cancer cell growth and causes G2M arrest, while not inducing compensation via OAT. In human tumors, ARG2 is highly expressed in specific tumor types, including basal-like breast tumors. This study sheds light on the interplay between metabolism and cell cycle and identifies ARG2 as a potential metabolic target.Entities:
Keywords: ARG2; OAT; arginase 2; basal-like breast cancer; cancer metabolism; isotope tracing; mass spectrometry; ornithine; polyamines
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Year: 2019 PMID: 30759381 PMCID: PMC6663478 DOI: 10.1016/j.celrep.2019.01.059
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423