Increased formate overflow is a hallmark of oxidative cancer

Nat Commun. 2018 Apr 10;9(1):1368. doi: 10.1038/s41467-018-03777-w.

Abstract

Formate overflow coupled to mitochondrial oxidative metabolism\ has been observed in cancer cell lines, but whether that takes place in the tumor microenvironment is not known. Here we report the observation of serine catabolism to formate in normal murine tissues, with a relative rate correlating with serine levels and the tissue oxidative state. Yet, serine catabolism to formate is increased in the transformed tissue of in vivo models of intestinal adenomas and mammary carcinomas. The increased serine catabolism to formate is associated with increased serum formate levels. Finally, we show that inhibition of formate production by genetic interference reduces cancer cell invasion and this phenotype can be rescued by exogenous formate. We conclude that increased formate overflow is a hallmark of oxidative cancers and that high formate levels promote invasion via a yet unknown mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoma / genetics
  • Adenoma / metabolism*
  • Adenoma / pathology
  • Animals
  • Antimetabolites, Antineoplastic / pharmacology
  • Cell Line, Tumor
  • Female
  • Formates / metabolism*
  • Formates / pharmacology
  • Gene Expression Regulation, Neoplastic*
  • Glycine Hydroxymethyltransferase / genetics
  • Glycine Hydroxymethyltransferase / metabolism
  • Intestinal Mucosa / metabolism
  • Intestinal Neoplasms / genetics
  • Intestinal Neoplasms / metabolism*
  • Intestinal Neoplasms / pathology
  • Intestines / pathology
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Male
  • Mammary Glands, Animal / metabolism
  • Mammary Glands, Animal / pathology
  • Mammary Glands, Animal / virology
  • Mammary Neoplasms, Experimental / drug therapy
  • Mammary Neoplasms, Experimental / genetics
  • Mammary Neoplasms, Experimental / metabolism*
  • Mammary Neoplasms, Experimental / virology
  • Mammary Tumor Virus, Mouse / pathogenicity
  • Methotrexate / pharmacology
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Oxidation-Reduction
  • Serine / metabolism*
  • Tumor Microenvironment / drug effects

Substances

  • Antimetabolites, Antineoplastic
  • Formates
  • Isoenzymes
  • formic acid
  • Serine
  • Glycine Hydroxymethyltransferase
  • Shmt1 protein, mouse
  • Methotrexate