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靶向微泡用于超声介导短发夹RNA质粒转染以抑制生存素基因表达并诱导卵巢癌A2780/DDP细胞凋亡

Targeted Microbubbles for Ultrasound Mediated Short Hairpin RNA Plasmid Transfection to Inhibit Survivin Gene Expression and Induce Apoptosis of Ovarian Cancer A2780/DDP Cells.

作者信息

Zhang Yong, Chang Shufang, Sun Jiangchuan, Zhu Shenyin, Pu Caixiu, Li Yaowei, Zhu Yi, Wang Zhigang, Xu Ronald X

机构信息

Department of Obstetrics and Gynecology, Second Affiliated Hospital of Chongqing Medical University , Chongqing 400010, China.

National Engineering Research Center of Ultrasound Medicine , Chongqing 400010, China.

出版信息

Mol Pharm. 2015 Sep 8;12(9):3137-45. doi: 10.1021/mp500835z. Epub 2015 Aug 3.

Abstract

Nonviral gene transfer by ultrasound-targeted microbubble destruction (UTMD) is an promising technique for RNA interference (RNAi) therapy. Targeting silence survivin gene may provide an important therapeutic option for patients with ovarian cancer. However, UTMD mediated RNAi therapy typically uses nontargeted microbubbles with suboptimal gene transfection efficiency. In this work, a LHRHa targeted microbubble agent and recombinant expression plasmid of shRNA targeting survivin gene (pshRNA survivin) were constructed for UTMD mediated pshRNA survivin therapy in ovarian cancer A2780/DDP cells that express LHRH receptors. The targeted microbubbles (TMBs) mixed with the pshRNA survivin were added to cultured ovarian cancer cells followed by ultrasound exposure (1 MHz, 0.5 W/cm(2)) for 30 s. After transfection for 48 h, the expression of survivin mRNA and protein were (0.36 ± 0.036) and (0.05 ± 0.02), respectively. The cell proliferation inhibitory rates at 24, 48, and 72 h after treatment are (42.08 ± 3.20)%, (54.60 ± 1.02)%, and (74.25 ± 2.14)%, respectively, and the apoptosis rate was (28.99 ± 2.70)%. The expression of apoptosis related protein caspase-9 and caspase-3 were (0.95 ± 0.09) and (2.6 ± 0.21). In comparison with the other treatment groups, ultrasound mediation of targeted microbubbles yielded higher RNAi efficiency and higher cell apoptosis rate and cell proliferation inhibitory rate (p < 0.05). Our experiment verifies the hypothesis that ultrasound mediation of targeted microbubbles will enhance RNAi efficiency in ovarian cancer cells. This novel method for RNA interference represents a powerful, promising no viral technology that can be used in the tumor gene therapy and research.

摘要

通过超声靶向微泡破坏(UTMD)进行的非病毒基因转移是一种用于RNA干扰(RNAi)治疗的有前景的技术。靶向沉默生存素基因可能为卵巢癌患者提供一种重要的治疗选择。然而,UTMD介导的RNAi治疗通常使用非靶向微泡,其基因转染效率欠佳。在本研究中,构建了一种促黄体激素释放激素激动剂(LHRHa)靶向的微泡剂和靶向生存素基因的短发夹RNA(shRNA)重组表达质粒(pshRNA survivin),用于在表达LHRH受体的卵巢癌A2780/DDP细胞中进行UTMD介导的pshRNA survivin治疗。将与pshRNA survivin混合的靶向微泡(TMBs)加入培养的卵巢癌细胞中,随后进行超声照射(1 MHz,0.5 W/cm²)30秒。转染48小时后,生存素mRNA和蛋白的表达分别为(0.36±0.036)和(0.05±0.02)。处理后24、48和72小时的细胞增殖抑制率分别为(42.08±3.20)%、(54.60±1.02)%和(74.25±2.14)%,凋亡率为(28.99±2.70)%。凋亡相关蛋白半胱天冬酶-9和半胱天冬酶-3的表达分别为(0.95±0.09)和(2.6±0.21)。与其他治疗组相比,超声介导的靶向微泡产生了更高的RNAi效率、更高的细胞凋亡率和细胞增殖抑制率(p<0.05)。我们的实验验证了超声介导的靶向微泡将提高卵巢癌细胞中RNAi效率的假设。这种新的RNA干扰方法代表了一种强大、有前景的非病毒技术,可用于肿瘤基因治疗和研究。

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