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CD147 subunit of lactate/H+ symporters MCT1 and hypoxia-inducible MCT4 is critical for energetics and growth of glycolytic tumors.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2011 Oct 04; Vol. 108 (40), pp. 16663-8. Date of Electronic Publication: 2011 Sep 19. - Publication Year :
- 2011
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Abstract
- Malignant tumors exhibit increased dependence on glycolysis, resulting in abundant export of lactic acid, a hypothesized key step in tumorigenesis. Lactic acid is mainly transported by two H(+)/lactate symporters, MCT1/MCT4, that require the ancillary protein CD147/Basigin for their functionality. First, we showed that blocking MCT1/2 in Ras-transformed fibroblasts with AR-C155858 suppressed lactate export, glycolysis, and tumor growth, whereas ectopic expression of MCT4 in these cells conferred resistance to MCT1/2 inhibition and reestablished tumorigenicty. A mutant-derivative, deficient in respiration (res(-)) and exclusively relying on glycolysis for energy, displayed low tumorigenicity. These res(-) cells could develop resistance to MCT1/2 inhibition and became highly tumorigenic by reactivating their endogenous mct4 gene, highlighting that MCT4, the hypoxia-inducible and tumor-associated lactate/H(+) symporter, drives tumorigenicity. Second, in the human colon adenocarcinoma cell line (LS174T), we showed that combined silencing of MCT1/MCT4 via inducible shRNA, or silencing of CD147/Basigin alone, significantly reduced glycolytic flux and tumor growth. However, both silencing approaches, which reduced tumor growth, displayed a low level of CD147/Basigin, a multifunctional protumoral protein. To gain insight into CD147/Basigin function, we designed experiments, via zinc finger nuclease-mediated mct4 and basigin knockouts, to uncouple MCTs from Basigin expression. Inhibition of MCT1 in MCT4-null, Basigin(high) cells suppressed tumor growth. Conversely, in Basigin-null cells, in which MCT activity had been maintained, tumorigenicity was not affected. Collectively, these findings highlight that the major protumoral action of CD147/Basigin is to control the energetics of glycolytic tumors via MCT1/MCT4 activity and that blocking lactic acid export provides an efficient anticancer strategy.
- Subjects :
- Basigin genetics
Cell Line, Tumor
Cell Proliferation drug effects
Cell Transformation, Neoplastic drug effects
DNA Primers genetics
Flow Cytometry
Fluorescent Antibody Technique
Gene Knockout Techniques
Gene Silencing
Humans
Immunohistochemistry
Monocarboxylic Acid Transporters antagonists & inhibitors
Monocarboxylic Acid Transporters genetics
Muscle Proteins genetics
Oxygen Consumption physiology
Protein Subunits genetics
Symporters antagonists & inhibitors
Symporters genetics
Thiophenes pharmacology
Uracil analogs & derivatives
Uracil pharmacology
Basigin metabolism
Cell Transformation, Neoplastic genetics
Glycolysis drug effects
Lactic Acid metabolism
Monocarboxylic Acid Transporters metabolism
Muscle Proteins metabolism
Protein Subunits metabolism
Symporters metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 108
- Issue :
- 40
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 21930917
- Full Text :
- https://doi.org/10.1073/pnas.1106123108