1. Academic Validation
  2. Fibroblast pyruvate carboxylase is required for collagen production in the tumour microenvironment

Fibroblast pyruvate carboxylase is required for collagen production in the tumour microenvironment

  • Nat Metab. 2021 Nov;3(11):1484-1499. doi: 10.1038/s42255-021-00480-x.
Simon Schwörer 1 Natalya N Pavlova  # 1 Francesco V Cimino  # 1 Bryan King 1 Xin Cai 1 Gina M Sizemore 2 3 Craig B Thompson 4
Affiliations

Affiliations

  • 1 Cancer Biology and Genetics Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • 2 The Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.
  • 3 Department of Radiation Oncology, The Ohio State University, Columbus, OH, USA.
  • 4 Cancer Biology and Genetics Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA. [email protected].
  • # Contributed equally.
Abstract

The aberrant production of collagen by fibroblasts is a hallmark of many solid tumours and can influence Cancer progression. How the mesenchymal cells in the tumour microenvironment maintain their production of extracellular matrix proteins as the vascular delivery of glutamine and glucose becomes compromised remains unclear. Here we show that pyruvate carboxylase (PC)-mediated anaplerosis in tumour-associated fibroblasts contributes to tumour fibrosis and growth. Using cultured mesenchymal and Cancer cells, as well as mouse allograft models, we provide evidence that extracellular lactate can be utilized by fibroblasts to maintain tricarboxylic acid (TCA) cycle anaplerosis and non-essential amino acid biosynthesis through PC activity. Furthermore, we show that fibroblast PC is required for collagen production in the tumour microenvironment. These results establish TCA cycle anaplerosis as a determinant of extracellular matrix collagen production, and identify PC as a potential target to inhibit tumour desmoplasia.

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