Mapping Metabolic Events in the Cancer Cell Cycle Reveals Arginine Catabolism in the Committed SGM Phase.

Cell Rep

Cardiovascular Medicine Unit, Department of Medicine, Karolinska Institutet, SE-171 76 Stockholm, Sweden; Division of Cardiovascular Medicine, Karolinska University Hospital, SE-171 76 Stockholm, Sweden; Center for Molecular Medicine, Karolinska Institutet, SE-171 76 Stockholm, Sweden. Electronic address:

Published: February 2019

AI Article Synopsis

  • Alterations in cell-cycle regulation and metabolism play a crucial role in cancer transformation, with specific enzymes representing potential vulnerabilities for targeting cancer cells.
  • The study uses advanced techniques like cell sorting and mass spectrometry to identify hundreds of metabolites involved in the G and SGM phases of the cell cycle, highlighting the significant role of arginine and ornithine.
  • The mitochondrial enzyme arginase 2 (ARG2) is identified as a key player in cancer cell metabolism, with its knockdown leading to reduced growth and cell cycle arrest in cancer cells, emphasizing its potential as a therapeutic target, especially in certain tumor types like basal-like breast cancer.

Article 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 G and SGM 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 SGM 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 GM 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6663478PMC
http://dx.doi.org/10.1016/j.celrep.2019.01.059DOI Listing

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