中华皮肤科杂志 ›› 2009, Vol. 42 ›› Issue (3): 189-192.

• 论著 • 上一篇    下一篇

靶向生存素的小干扰RNA抑制人黑素瘤M14细胞系生长的研究

宋琳毅 孙建方 周武庆 曾学思   

  1. 苏州大学附属第一医院 南京医科院皮研所 南京医科院皮研所 南京医科院皮研所
  • 收稿日期:2008-04-07 修回日期:2008-05-11 出版日期:2009-03-15 发布日期:2009-03-15
  • 通讯作者: 宋琳毅 E-mail:linyis28@163.com

Inhibitory effects of siRNA targeting survivin on the growth of a human melanoma cell line, M14

  • Received:2008-04-07 Revised:2008-05-11 Online:2009-03-15 Published:2009-03-15

摘要:

目的 探讨小干扰RNA(siRNA)对人黑素瘤M14细胞系生存素基因表达的抑制作用及对细胞凋亡、增殖和侵袭的影响。方法 构建靶向生存素的siRNA表达质粒,用脂质体法转染M14人黑素瘤细胞。RT-PCR检测M14细胞生存素mRNA的表达,Western印迹检测生存素蛋白的表达,流式细胞仪检测AnexinV标记的凋亡细胞,噻唑蓝(MTT)法分析细胞增殖,Transwell法分析侵袭能力。结果 与M14细胞和转染空载体的M14细胞比较,转染siRNA的表达质粒可以明显抑制生存素基因在转录和翻译上的表达。M14组和空载体组几乎无凋亡细胞,siRNA表达质粒组的凋亡率明显增加(χ2 = 31.55,P < 0.01)。细胞增殖抑制率(63.6% ± 1.6%)也明显增加,同时Transwell细胞侵袭实验显示,siRNA表达质粒转染组抑制作用显著。结论 靶向生存素的siRNA表达质粒可以特异性抑制生存素的表达,显著抑制肿瘤细胞增殖和侵袭并诱导细胞凋亡。

关键词: Survivin基因;RNA干扰;黑素瘤;凋亡;增殖;侵袭

Abstract:

Objective To study the inhibitory effects of siRNA targeting survivin on the expression of survivin, as well as the apoptosis, proliferation and invasion of a human melanoma cell line, M14. Methods Two siRNAs targeting survivin were designed, chemically synthesized, and used to construct the recombinant plasmids, pRNAT-H1.1/neo-survivin-siRNA1 and pRNAT-H1.1/neo-survivin-siRNA2. Then, recombinant plasmids were transfected into M14 cells mediated by Lipofectamine 2000 reagent. Those cells untransfected or transfected with empty vector served as the control. After culture over various periods of time, cells were collected for the detection of mRNA and protein expression of survivin with RT-PCR and Western blotting, respectively, and for the examination of apoptosis and proliferation of M14 cells by flow cytometry and MTT methods, respectively. Also, Transwell assay was performed to detect the invasive capability of M14 cells. Results A statistical decrease in the mRNA and protein expressions of survivin was observed along with an increase in apoptotic rate (χ2 = 31.55, P < 0.01) in M14 cells transfected with siRNA-containing plasmid compared with untransfected and empty vector-transfected cells. As MTT assay indicated, on day 4 after the transfection, the proliferation of M14 cells was inhibited by (55.4 ± 4.3)%, (34.5 ± 4.3)% and (13.3 ± 4.6)%, with pRNAT-H1.1/neo-survivin-siRNA1, pRNAT-H1.1/neo-survivin- siRNA2 and empty vector, respectively; there was a significant difference among the three groups (P < 0.05). Decreased invasive capability was noticed in M14 cells transfected with siRNA-containing plasmid compared with untransfected cells (all P < 0.05). Conclusions The plasmid containing siRNA against survivin can specifically inhibit the expression of survivin, proliferation and invasion of tumor cells, and induce cell apoptosis. The inhibition of survivin expression by siRNA may be a rational approach to the gene therapy for malignant melanoma.

Key words: Survivin;siRNA;melanoma;apoptosis;proliferation;invasion