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靛玉红抑制乳腺癌细胞中的多药耐药蛋白1并逆转阿霉素耐药性。

Tryptanthrin inhibits MDR1 and reverses doxorubicin resistance in breast cancer cells.

作者信息

Yu Sung-Tsai, Chen Tzer-Ming, Tseng Shih-Yun, Chen Yen-Hui

机构信息

Graduate Institute of Pharmaceutical Sciences, College of Medicine, National Taiwan University, Taipei 10051, Taiwan.

出版信息

Biochem Biophys Res Commun. 2007 Jun 22;358(1):79-84. doi: 10.1016/j.bbrc.2007.04.107. Epub 2007 Apr 26.

Abstract

Development of agents to overcome multidrug resistance (MDR) is important in cancer chemotherapy. Up to date, few chemicals have been reported to down-regulate MDR1 gene expression. We evaluated the effect of tryptanthrin on P-glycoprotein (P-gp)-mediated MDR in a breast cancer cell line MCF-7. Tryptanthrin could depress overexpression of MDR1 gene. We observed reduction of P-gp protein in parallel with decreases in mRNA in MCF-7/adr cells treated with tryptanthrin. Tryptanthrin suppressed the activity of MDR1 gene promoter. Tryptanthrin also enhanced interaction of the nuclear proteins with the negatively regulatory CAAT region of MDR1 gene promoter in MCF-7/adr. It might result in suppression of MDR1 gene. In addition, tryptanthrin decreased the amount of mutant p53 protein with decreasing mutant p53 protein stability. It might contribute to negative regulation of MDR1 gene. In conclusion, tryptanthrin exhibited MDR reversing effect by down-regulation of MDR1 gene and might be a new adjuvant agent for chemotherapy.

摘要

开发能够克服多药耐药性(MDR)的药物在癌症化疗中具有重要意义。到目前为止,据报道很少有化学物质能够下调MDR1基因的表达。我们评估了色胺酮对乳腺癌细胞系MCF-7中P-糖蛋白(P-gp)介导的多药耐药性的影响。色胺酮能够抑制MDR1基因的过表达。我们观察到,在用色胺酮处理的MCF-7/adr细胞中,P-gp蛋白减少,同时mRNA水平也下降。色胺酮抑制了MDR1基因启动子的活性。色胺酮还增强了核蛋白与MCF-7/adr中MDR1基因启动子负调控CAAT区域的相互作用。这可能导致MDR1基因受到抑制。此外,色胺酮减少了突变型p53蛋白的量,同时降低了突变型p53蛋白的稳定性。这可能有助于对MDR1基因进行负调控。总之,色胺酮通过下调MDR1基因表现出多药耐药逆转作用,可能成为一种新的化疗辅助药物。

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