Blocking CD147 induces cell death in cancer cells through impairment of glycolytic energy metabolism

被引:110
作者
Baba, Miyako [1 ]
Inoue, Masahiro [2 ]
Itoh, Kazuyuki [3 ]
Nishizawa, Yasuko [1 ]
机构
[1] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Pathol, Res Inst, Higashinari Ku, Osaka 5378511, Japan
[2] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Tumor Biochem, Res Inst, Higashinari Ku, Osaka 5378511, Japan
[3] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Biol, Res Inst, Higashinari Ku, Osaka 5378511, Japan
关键词
CD147; cell death; MCT-1; acidosis; glycolytic energy metabolism;
D O I
10.1016/j.bbrc.2008.06.122
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
CD 147 is a multifunctional transmembrane protein and promotes cancer progression. We found that the anti-human CD147 mouse monoclonal antibody MEM-M6/1 strongly induces necrosis-like cell death in LoVo, HT-29, WiDr, and SW620 colon cancer cells and A2058 melanoma cells, but not in WI-38 and TIG-113 normal fibroblasts. Silencing or overexpression of CD147 in LoVo cells enhanced or decreased the MEM-M6/1 induced cell death, respectively. CD147 is known to form complex with proton-linked monocarboxylate transporters (MCTs), which is critical for lactate transport and intracellular pH (pHi) homeostasis : In LoVo cells, CD147 and MCT-1 co-localized on the cell Surface, and MEM-M6/1 inhibited the association of these molecules. MEM-M6/1 inhibited lactate uptake, lactate release, and reduced pHi. Further, the induction of acidification was parallel to the decrease of the glycolytic flux and intracellular ATP levels. These effects were not found in the normal fibroblasts. As cancer cells depend oil glycolysis for their energy production, CD147 inhibition might induce cell death specific to cancer cells. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:111 / 116
页数:6
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