4.6 Article

The reverse Warburg effect Aerobic glycolysis in cancer associated fibroblasts and the tumor stroma

期刊

CELL CYCLE
卷 8, 期 23, 页码 3984-4001

出版社

TAYLOR & FRANCIS INC
DOI: 10.4161/cc.8.23.10238

关键词

caveolin-1; tumor stroma; myo-fibroblast; cancer-associated fibroblast; aerobic glycolysis; M2-isoform of pyruvate kinase; lactate dehydrogenase; Warburg effect

资金

  1. NIH/NCI [R01-CA-80250, R01-CA-098779, R01-CA-120876, R01-AR-055660, R01-CA-70896, R01-CA-75503, R01-CA-86072, R01-CA-107382, P30-CA-56036]
  2. Susan G. Komen Breast Cancer Foundation
  3. Department of Defense-Breast Cancer Research Program (Synergistic Idea Award)
  4. Breast Cancer Alliance, Inc.
  5. Susan G. Komen Career Catalyst Grant
  6. W.W. Smith Charitable Trust
  7. Breast Cancer Alliance (BCA)
  8. American Cancer Society (ACS)
  9. Dr. Ralph and Marian C. Falk Medical Research Trust
  10. Margaret Q. Landenberger Research Foundation
  11. Pennsylvania Department of Health

向作者/读者索取更多资源

Here, we propose a new model for understanding the Warburg effect in tumor metabolism. Our hypothesis is that epithelial cancer cells induce the Warburg effect (aerobic glycolysis) in neighboring stromal fibroblasts. These cancer-associated fibroblasts, then undergo myo-fibroblastic differentiation, and secrete lactate and pyruvate (energy metabolites resulting from aerobic glycolysis). Epithelial cancer cells could then take up these energy-rich metabolites and use them in the mitochondrial TCA cycle, thereby promoting efficient energy production (ATP generation via oxidative phosphorylation), resulting in a higher proliferative capacity. In this alternative model of tumorigenesis, the epithelial cancer cells instruct the normal stroma to transform into a wound-healing stroma, providing the necessary energy-rich micro-environment for facilitating tumor growth and angiogenesis. In essence, the fibroblastic tumor stroma would directly feed the epithelial cancer cells, in a type of host-parasite relationship. We have termed this new idea the Reverse Warburg Effect. In this scenario, the epithelial tumor cells corrupt the normal stroma, turning it into a factory for the production of energy-rich metabolites. This alternative model is still consistent with Warburg's original observation that tumors show a metabolic shift towards aerobic glycolysis. In support of this idea, unbiased proteomic analysis and transcriptional profiling of a new model of cancer-associated fibroblasts (caveolin-1 (Cav-1) deficient stromal cells), shows the upregulation of both (1) myo-fibroblast markers and (2) glycolytic enzymes, under normoxic conditions. We validated the expression of these proteins in the fibroblastic stroma of human breast cancer tissues that lack stromal Cav-1. Importantly, a loss of stromal Cav-1 in human breast cancers is associated with tumor recurrence, metastasis, and poor clinical outcome. Thus, an absence of stromal Cav-1 may be a biomarker for the Reverse Warburg Effect, explaining its powerful predictive value.

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