4.7 Article

Molecular Pathways: Trafficking of Metabolic Resources in the Tumor Microenvironment

Journal

CLINICAL CANCER RESEARCH
Volume 21, Issue 4, Pages 680-686

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-14-2198

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Funding

  1. Eunice Kennedy Shriver National Institute of Child Health and Human Development of the NIH [K12HD000849]
  2. American Board of Obstetrics and Gynecology
  3. NCI of the NIH [R01CA111882, R01CA169604]
  4. Bears Care, the charitable beneficiary of the Chicago Bears Football Club

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A model of tumor metabolism is proposed that describes how the complementary metabolic functions of the local stroma and the tumor cells contribute to cancer progression. Cancer cells alter the metabolism of cancer-associated fibroblasts to obtain lactate and amino acids, which are utilized for energy production, rapid growth, and resistance to chemotherapy drugs. Cancer cells use glutamine supplied by cancer-associated fibroblasts to replenish tricarboxylic acid cycle intermediates and as a nitrogen source for nucleotide synthesis. Moreover, adipocytes in the microenvironment attract cancer cells through the secretion of inflammatory cytokines and proteases. The cancer cells then induce metabolic changes in the adipocytes to acquire free fatty acids that are oxidized by cancer cells to generate energy for proliferation. Increasing knowledge about the metabolic symbiosis within the tumor has led to novel therapeutic strategies designed to restrict metabolic adaptation, including inhibiting lactate transporters and repurposing antidiabetic drugs (thiazolidinediones, metformin). (C)2015 AACR.

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