Differential effect of glucose derivation on MAPK activation in drug sensitive human breast carcinoma MCF-7 and multidrug resistant MCF-7/ADR cells

被引:21
作者
Gupta, AK
Lee, YJ
Galoforo, SS
Berns, CM
Martinez, AA
Corry, PM
Wu, XY
Guan, KL
机构
[1] WILLIAM BEAUMONT HOSP,DEPT RADIAT ONCOL,RES LABS,ROYAL OAK,MI 48073
[2] UNIV MICHIGAN,DEPT BIOL CHEM,ANN ARBOR,MI 48109
[3] UNIV MICHIGAN,INST GERONTOL,ANN ARBOR,MI 48109
关键词
glucose deprivation; MAPK; MCF-7; MCF-7/ADR; signal transduction;
D O I
10.1023/A:1006890316102
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have investigated the effect of glucose deprivation treatment on the activation of mitogen activated protein kinases (MAPKs) in the drug-sensitive human breast carcinoma cells (MCF-7) and its drug resistant variant (MCF-7/ADR) cells. Western blots and in-gel kinase assays showed that glucose free medium was a strong stimulus for the activation of MAPK in MCF-7/ADR cells. No activation was seen in MCF-7 cells. MAPK was activated within 3 min of being in glucose free medium and it remained activated for over 1 h in MCF-7/ADR cells. After being returned to complete medium, 1 h was required for the MAPK to become deactivated. To investigate whether alternative sources of ATP could inhibit glucose deprivation induced MAPK activation, we added glutamine and glutamate to glucose deprived medium. The addition of glutamine did not reverse glucose deprivation induced MAPK activation in MCF-7/ADR cells, The addition of glutamate, however, decreased the MAPK activation and the length of time of activation. We observed an increase greater than three fold in MEK, Raf, Ras, and PKC activity with glucose deprivation in MCF-7/ADR cells. This suggests that glucose deprivation-induced MAPK activation is mediated through this signal transduction pathway.
引用
收藏
页码:23 / 30
页数:8
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