The phytoestrogen genistein enhances multidrug resistance in breast cancer cell lines by translational regulation of ABC transporters

被引:52
|
作者
Rigalli, Juan Pablo [1 ,2 ]
Tocchetti, Guillermo Nicolas [2 ]
Arana, Maite Rocio [2 ]
Villanueva, Silvina Stella Maris [2 ]
Catania, Viviana Alicia [2 ]
Theile, Dirk
Ruiz, Maria Laura [2 ]
Weiss, Johanna [1 ]
机构
[1] Heidelberg Univ, Dept Clin Pharmacol & Pharmacoepidemiol, Neuenheimer Feld 410, D-69120 Heidelberg, Germany
[2] Rosario Natl Univ, Fac Biochem & Pharmaceut Sci, Inst Expt Physiol, Suipacha 570, RA-2000 Rosario, Santa Fe, Argentina
关键词
Breast cancer; Genistein; Multidrug resistance; Translational regulation; Chemoresistance; TYROSINE-KINASE INHIBITOR; PREGNANE-X-RECEPTOR; DRUG TRANSPORTERS; UP-REGULATION; LUNG-CANCER; EXPRESSION; PROTEIN; ISOFLAVONES; MRP2; DOXORUBICIN;
D O I
10.1016/j.canlet.2016.03.040
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer is the most frequent malignancy in women. Multidrug resistance due to overexpression of ABC drug transporters is a common cause of chemotherapy failure and disease recurrence. Genistein (GNT) is a phytoestrogen present in soybeans and hormone supplements. We investigated the effect of GNT on the expression and function of ABC transporters in MCF-7 and MDA-MB-231 breast cancer cell lines. Results demonstrated an induction at the protein level of ABCC1 and ABCG2 and of ABCC1 in MCF-7 and MDA-MB-231, respectively. MCF-7 cells showed a concomitant increase in doxorubicin and mitoxantrone efflux and resistance, dependent on ABCG2 activity. ABCC1 induction by GNT in MDA-MB-231 cells modified neither drug efflux nor chemoresistance due to simultaneous acute inhibition of the transporter activity by GNT. All inductions took place at the translational level, as no increment in mRNA was observed and protein increase was prevented by cycloheximide. miR-181a, already demonstrated to inhibit ABCG2 translation, was down-regulated by GNT, explaining translational induction. Effects were independent of classical estrogen receptors. Results suggest potential nutrient drug interactions that could threaten chemotherapy efficacy, especially in ABCG2-expressing tumors treated with substrates of this transporter. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:165 / 172
页数:8
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