Wang X M, Gao S J, Guo X F, Sun W J, Yan Z Q, Wang W X, Xu Y Q, Lu D
Department of Oncology, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.
Department of Breast Surgery, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.
Braz J Med Biol Res. 2014 Apr;47(4):273-8. doi: 10.1590/1414-431x20133356. Epub 2014 Mar 21.
Overexpression of cytokine-induced apoptosis inhibitor 1 (CIAPIN1) contributes to multidrug resistance (MDR) in breast cancer. This study aimed to evaluate the potential of CIAPIN1 gene silencing by RNA interference (RNAi) as a treatment for drug-resistant breast cancer and to investigate the effect of CIAPIN1 on the drug resistance of breast cancer in vivo. We used lentivirus-vector-based RNAi to knock down CIAPIN1 in nude mice bearing MDR breast cancer tumors and found that lentivirus-vector-mediated silencing of CIAPIN1 could efficiently and significantly inhibit tumor growth when combined with chemotherapy in vivo. Furthermore, Western blot analysis showed that both CIAPIN1 and P-glycoprotein expression were efficiently downregulated, and P53 was upregulated, after RNAi. Therefore, we concluded that lentivirus-vector-mediated RNAi targeting of CIAPIN1 is a potential approach to reverse MDR of breast cancer. In addition, CIAPIN1 may participate in MDR of breast cancer by regulating P-glycoprotein and P53 expression.
细胞因子诱导的凋亡抑制因子1(CIAPIN1)的过表达导致乳腺癌的多药耐药(MDR)。本研究旨在评估通过RNA干扰(RNAi)沉默CIAPIN1基因作为耐药乳腺癌治疗方法的潜力,并研究CIAPIN1在体内对乳腺癌耐药性的影响。我们使用基于慢病毒载体的RNAi在携带MDR乳腺癌肿瘤的裸鼠中敲低CIAPIN1,发现慢病毒载体介导的CIAPIN1沉默在体内与化疗联合使用时能够有效且显著地抑制肿瘤生长。此外,蛋白质印迹分析表明,RNAi后CIAPIN1和P-糖蛋白的表达均有效下调,而P53上调。因此,我们得出结论,慢病毒载体介导的针对CIAPIN1的RNAi是逆转乳腺癌MDR的一种潜在方法。此外,CIAPIN1可能通过调节P-糖蛋白和P53的表达参与乳腺癌的MDR。
Braz J Med Biol Res. 2014-4
J Control Release. 2017-3-14
Curr Treat Options Oncol. 2012-6
Ann Oncol. 2012-4-6
J Nucleic Acids. 2012
Biochem Biophys Res Commun. 2011-6-12
Mini Rev Med Chem. 2011-2
Curr Opin Pharmacol. 2010-7-9
Expert Opin Ther Targets. 2010-6