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P-glycoprotein down-regulates expression of breast cancer resistance protein in a drug-free state
Authors:Bark Hyun  Xu Hai-Dong  Kim Sang-Hyun  Yun Jisoo  Choi Cheol-Hee
Institution:Research Center for Resistant Cells and Department of Pharmacology, Chosun University Medical School, Gwangju, Republic of Korea.
Abstract:This study investigated whether P-glycoprotein (Pgp) and breast cancer resistance protein (BCRP) are linked in terms of expression. RT-PCR and Western blot analyses showed that the lung cancer cell line SK-MES-1/WT expressed BCRP. In a drug-free state, BCRP expression was significantly down-regulated in doxorubicin-resistant SK-MES-1/DX1000 cells overexpressing Pgp. Pharmacological inhibitors (PSC833 or verapamil) or siRNA for Pgp inhibited the down-regulation of BCRP, which was confirmed by confocal microscopy. PSC833 induced the phosphorylation of c-Jun NH2-terminal kinase (JNK) and c-Jun, while the JNK inhibitor SP600125 inhibited this effect. Dominant negative c-Jun decreased the expression of BCRP, but increased that of Pgp. These results indicate that Pgp down-regulates BCRP expression in a drug-free state in which JNK/c-Jun is involved.
Keywords:MDR  multidrug resistance  Pgp  P-glycoprotein  MRP1  multidrug resistance-associated protein 1  BCRP  breast cancer resistance protein  ABC  ATP-binding cassette  JNK  c-Jun NH2-terminal kinase  MAPK  mitogen-activated protein kinase  DN-c-Jun  dominant negative form of c-Jun
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