Tissue of origin dictates branched-chain amino acid metabolism in mutant Kras-driven cancers

Science. 2016 Sep 9;353(6304):1161-5. doi: 10.1126/science.aaf5171.

Abstract

Tumor genetics guides patient selection for many new therapies, and cell culture studies have demonstrated that specific mutations can promote metabolic phenotypes. However, whether tissue context defines cancer dependence on specific metabolic pathways is unknown. Kras activation and Trp53 deletion in the pancreas or the lung result in pancreatic ductal adenocarinoma (PDAC) or non-small cell lung carcinoma (NSCLC), respectively, but despite the same initiating events, these tumors use branched-chain amino acids (BCAAs) differently. NSCLC tumors incorporate free BCAAs into tissue protein and use BCAAs as a nitrogen source, whereas PDAC tumors have decreased BCAA uptake. These differences are reflected in expression levels of BCAA catabolic enzymes in both mice and humans. Loss of Bcat1 and Bcat2, the enzymes responsible for BCAA use, impairs NSCLC tumor formation, but these enzymes are not required for PDAC tumor formation, arguing that tissue of origin is an important determinant of how cancers satisfy their metabolic requirements.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acids, Branched-Chain / metabolism*
  • Animals
  • Carcinoma, Non-Small-Cell Lung / genetics*
  • Carcinoma, Non-Small-Cell Lung / metabolism*
  • Carcinoma, Pancreatic Ductal / genetics*
  • Carcinoma, Pancreatic Ductal / metabolism*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Lung Neoplasms / genetics*
  • Lung Neoplasms / metabolism*
  • Male
  • Metabolic Networks and Pathways
  • Mice
  • Mice, Inbred C57BL
  • Minor Histocompatibility Antigens / genetics
  • Mutation
  • Nitrogen / metabolism
  • Organ Specificity
  • Pancreatic Neoplasms / genetics*
  • Pancreatic Neoplasms / metabolism*
  • Pregnancy Proteins / genetics
  • Proto-Oncogene Proteins p21(ras) / genetics*
  • Transaminases / genetics

Substances

  • Amino Acids, Branched-Chain
  • KRAS protein, human
  • Minor Histocompatibility Antigens
  • Pregnancy Proteins
  • BCAT1 protein, human
  • Transaminases
  • BCAT2 protein, human
  • Proto-Oncogene Proteins p21(ras)
  • Nitrogen