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Serine racemase enhances growth of colorectal cancer by producing pyruvate from serine.

Abstract
Serine racemase (SRR) catalyses not only the racemization but also the dehydration of L-serine and D-serine, resulting in the formation of pyruvate and ammonia. Although SRR activity is important in the central nervous system, SRR has not been linked to cancer metabolism before. Here we show that SRR supports proliferation of colorectal-cancer cells. We find that SRR expression is upregulated in colorectal adenoma and adenocarcinoma lesions compared with non-neoplastic mucosa in human colorectal-cancer specimens. SRR-mediated dehydration of serine contributes to the pyruvate pool in colon-cancer cells, enhances proliferation, maintains mitochondrial mass and increases basal reactive oxygen species production, which has anti-apoptotic effects. Moreover, SRR promotes acetylation of histone H3 by maintaining intracellular acetyl-CoA levels. Inhibition of SRR suppresses growth of colorectal tumours in mice and augments the efficacy of 5-fluorouracil treatment. Our findings highlight a previously unknown mechanism through which a racemase supports cancer-cell growth and suggest that SRR might be a molecular target for colorectal-cancer therapy.
AuthorsKenji Ohshima, Satoshi Nojima, Shinichiro Tahara, Masako Kurashige, Keisuke Kawasaki, Yumiko Hori, Moyu Taniguchi, Yutaka Umakoshi, Daisuke Okuzaki, Naoki Wada, Jun-Ichiro Ikeda, Eiichiro Fukusaki, Eiichi Morii
JournalNature metabolism (Nat Metab) Vol. 2 Issue 1 Pg. 81-96 (01 2020) ISSN: 2522-5812 [Electronic] Germany
PMID32694681 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • RNA, Messenger
  • Serine
  • Pyruvic Acid
  • Racemases and Epimerases
  • serine racemase
Topics
  • Animals
  • Cell Line, Tumor
  • Cell Proliferation
  • Colorectal Neoplasms (metabolism, pathology)
  • Heterografts
  • Humans
  • Mice
  • Mice, Nude
  • Pyruvic Acid (metabolism)
  • RNA, Messenger (genetics)
  • Racemases and Epimerases (genetics, metabolism)
  • Serine (metabolism)
  • Up-Regulation

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