∼- elemene, a compound derived from Rhizoma zedoariae, reverses multidrug resistance mediated by the ABCB1 transporter

被引:49
作者
Guo, Hui-Qin [1 ,2 ]
Zhang, Guan-Nan [2 ]
Wang, Yi-Jun [2 ]
Zhang, Yun-Kai [2 ]
Sodani, Kamlesh [2 ]
Talele, Tanaji T. [2 ]
Ashby, Charles R., Jr. [2 ]
Chen, Zhe-Sheng [2 ]
机构
[1] Beijing Union Med Coll Hosp, Dept Thorac Surg, Beijing 100730, Peoples R China
[2] St Johns Univ, Dept Pharmaceut Sci, Coll Pharm & Hlth Sci, Queens, NY 11439 USA
关键词
ABCB1; multidrug resistance; -elemene; ABCB1-MEDIATED DRUG-RESISTANCE; P-GLYCOPROTEIN ABCB1; CANCER-CELLS; BETA-ELEMENE; TUMOR-CELLS; IN-VITRO; INHIBITORS; BINDING; LINES; VINCRISTINE;
D O I
10.3892/or.2013.2870
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the present in vitro study, we examined the effect of the compound -elemene on the response of KB-C2 cells overexpressing the ABCB1 transporter to specific antineoplastic compounds. The MTT assay was used to determine the effects of -elemene in combination with other anticancer drugs on ABCB1-overexpressing cancer cell lines. Furthermore, we used [H-3]-paclitaxel accumulation, efflux assay, immunofluorescence experiments, western blot assays and docking analysis to ascertain the mechanism of action of -elemene. The incubation of KB-C2 cells overexpressing ABCB1 transporter with -elemene (100 M) significantly augmented the antineoplastic efficacy of colchicine, vinblastine and paclitaxel when compared to KB-C2 cells incubated with these drugs alone. In HEK293 cells overexpressing the ABCB1 transporter, -elemene significantly increased the cytotoxicity of paclitaxel. In addition, 100 M of -elemene significantly increased the accumulation of [H-3]-paclitaxel and this was due to a decrease in [H-3]-paclitaxel efflux when compared to controls. The incubation of KB-C2 cells with -elemene (100 M) for 72 h did not significantly alter the expression of ABCB1 protein levels. Immunofluorescence experiments indicated that -elemene did not significantly alter the subcellular localization of the ABCB1 transporter. Docking analysis indicated that -elemene binds to the drug-binding site of ABCB1 transporter. Finally, -elemene at 100 M partially (similar to 50%) increased the sensitivity of the BCRP-overexpressing cell line, NCI-H460/MX20, to mitoxantrone, but -elemene did not significantly alter the resistance of MRP1-transfected HEK293/MRP1 cells to vincristine. Overall, our in vitro findings indicated that -elemene potentiates the cytotoxic effects of various antineoplastic drugs in cell lines overexpressing the ABCB1 transporter and that this is due to the inhibition of the efflux component of the ABCB1 transporter.
引用
收藏
页码:858 / 866
页数:9
相关论文
共 43 条
[1]   ISOLATION AND GENETIC-CHARACTERIZATION OF HUMAN KB-CELL LINES RESISTANT TO MULTIPLE-DRUGS [J].
AKIYAMA, SI ;
FOJO, A ;
HANOVER, JA ;
PASTAN, I ;
GOTTESMAN, MM .
SOMATIC CELL AND MOLECULAR GENETICS, 1985, 11 (02) :117-126
[2]   Structure of P-Glycoprotein Reveals a Molecular Basis for Poly-Specific Drug Binding [J].
Aller, Stephen G. ;
Yu, Jodie ;
Ward, Andrew ;
Weng, Yue ;
Chittaboina, Srinivas ;
Zhuo, Rupeng ;
Harrell, Patina M. ;
Trinh, Yenphuong T. ;
Zhang, Qinghai ;
Urbatsch, Ina L. ;
Chang, Geoffrey .
SCIENCE, 2009, 323 (5922) :1718-1722
[3]   P-glycoprotein: from genomics to mechanism [J].
Ambudkar, SV ;
Kimchi-Sarfaty, C ;
Sauna, ZE ;
Gottesman, MM .
ONCOGENE, 2003, 22 (47) :7468-7485
[4]  
BIEDLER JL, 1970, CANCER RES, V30, P1174
[5]  
BOESCH D, 1991, CANCER RES, V51, P4226
[6]  
CARMICHAEL J, 1987, CANCER RES, V47, P943
[7]   EXPRESSION OF THE MULTIDRUG RESISTANCE GENE-PRODUCT (P-GLYCOPROTEIN) IN HUMAN NORMAL AND TUMOR-TISSUES [J].
CORDONCARDO, C ;
OBRIEN, JP ;
BOCCIA, J ;
CASALS, D ;
BERTINO, JR ;
MELAMED, MR .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1990, 38 (09) :1277-1287
[8]   Lapatinib (Tykerb, GW572016) reverses multidrug resistance in cancer cells by inhibiting the activity of ATP-binding cassette subfamily B member 1 and G member 2 [J].
Dai, Chun-ling ;
Tiwari, Amit K. ;
Wu, Chung-Pu ;
Su, Xiao-dong ;
Wang, Si-Rong ;
Liu, Dong-geng ;
Ashby, Charles R., Jr. ;
Huang, Yan ;
Robey, Robert W. ;
Liang, Yong-ju ;
Chen, Li-ming ;
Shi, Cheng-Jun ;
Ambudkar, Suresh V. ;
Chen, Zhe-Sheng ;
Fu, Li-wu .
CANCER RESEARCH, 2008, 68 (19) :7905-7914
[9]   Considerations in the design and development of transport inhibitors as adjuncts to drug therapy [J].
Dantzig, AH ;
de Alwis, DP ;
Burgess, M .
ADVANCED DRUG DELIVERY REVIEWS, 2003, 55 (01) :133-150
[10]   Cyclosporine A enables vincristine-induced apoptosis during reversal of multidrug resistance phenotype in chronic myeloid leukemia cells [J].
de Souza, Paloma Silva ;
Vasconcelos, Flavia da Cunha ;
Silva, Luis Felipe R. ;
Maia, Raquel Ciuvalschi .
TUMOR BIOLOGY, 2012, 33 (04) :943-956