Metabolite Profiling Identifies a Key Role for Glycine in Rapid Cancer Cell Proliferation

Author:

Jain Mohit1234,Nilsson Roland1235,Sharma Sonia6,Madhusudhan Nikhil123,Kitami Toshimori123,Souza Amanda L.1,Kafri Ran2,Kirschner Marc W.2,Clish Clary B.1,Mootha Vamsi K.123

Affiliation:

1. Broad Institute, Cambridge, MA 02142, USA.

2. Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.

3. Center for Human Genetic Research and Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, USA.

4. Division of Cardiovascular Medicine, Department of Medicine, Brigham and Women’s Hospital, Boston, MA 02115, USA.

5. Unit of Computational Medicine, Department of Medicine, Karolinska Institutet, 17176 Stockholm, Sweden.

6. La Jolla Institute for Allergy & Immunology, La Jolla, CA 92037, USA.

Abstract

More Glycine, Please To better characterize metabolic properties of cancer cells, Jain et al. (p. 1040 ; see the Perspective by Tomita and Kami ) measured systematically the concentrations of hundreds of metabolites in cell culture medium in which 60 different cancer cell lines were growing. The fastest growing cancer cells tended to consume glycine, whereas more slowly growing cells excreted some glycine. The rapidly growing cancer cells appeared to need glycine for synthesis of purine nucleotides required for continued synthesis of DNA. Interfering with glycine metabolism slowed growth of the rapidly proliferating cancer cells. Thus, an increased dependence on glycine by rapidly growing cancer cells could potentially provide a target for therapeutic intervention.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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