Psychological stress induces chemoresistance in breast cancer by upregulating mdr1

被引:62
作者
Su, FX
Ouyang, NY
Zhu, PC
Ouyang, NT
Jia, WJ
Gong, C
Ma, XX
Xu, HB
Song, EW [1 ]
机构
[1] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Breast Surg, Guangzhou 510120, Peoples R China
[2] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Gynecol, Guangzhou 510120, Peoples R China
[3] Fudan Univ, Inst Genet, Shanghai 200433, Peoples R China
[4] Harvard Univ, Sch Med, CBR Inst Biomed Res, Boston, MA 02115 USA
[5] Guangzhou Med Inst, Dept Pathol, Guangzhou 510120, Peoples R China
基金
中国国家自然科学基金;
关键词
psychological stress; restraint stress; breast cancer; chemotherapy; multi-drug resistance; adrenaline; RNA interference;
D O I
10.1016/j.bbrc.2005.02.056
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
Psychological distress reduces the efficacy of chemotherapy in breast cancer patients. The mechanism may be related to the altered neuronal or hormonal secretions during stress. Here, we reported that adrenaline, a hormone mediating the biological activities of stress, upregulates mdr1 gene expression in MCF-7 breast cancer cells via alpha(2)-adrenerdric receptors in a dose-dependent manner. Mdr1 upregulation can be specifically inhibited by pretreatment with mdr1-siRNA. Consequently, adrenergic stimulation enhances the pump function of P-glycoprotein and confers resistance of MCF-7 cells to paclitaxel. In vivo, restraint stress increases mdr1 gene expression in the MCF-7 cancers that are inoculated subcutaneously into the SCID mice and provokes resistance to doxorubicin in the implanted tumors. The effect can be blocked by injection of yohimbine, an alpha(2)-adrenergic inhibitor, but not by metyrapone, a corticosterone synthesis blocker. Therefore, we conclude that breast cancers may develop resistance against chemotherapeutic drugs under psychological distress by over-expressing mdr1 via adrenergic stimulation. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:888 / 897
页数:10
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