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国家自然科学基金(30500506)

作品数:3 被引量:3H指数:1
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Lentivirus-mediated SMO RNA interference inhibits SMO expression and cell proliferation,and affects the cell cycle in LNCaP and PC3 cancer cell lines被引量:1
2010年
Smoothened (SMO) is an important member of the Hedgehog signaling pathway. We constructed a specific recombinant lentiviral vector for RNA interference,targeting the SMO gene (NM_005631) to observe its effect on SMO expression,cell proliferation and the cell cycle in the human androgen-sensitive prostate cancer cell line,LNCaP,and in the androgen-independent prostate cancer cell line,PC3. Four siRNA sequences were designed and inserted into a lentiviral vector pGCSIL-GFP to construct four recombinant vectors. The vector with the highest interfering efficiency was co-transfected with packaging vectors (pHelper1.0 and pHelper2.0) in 293T cells to assemble lentivirus particles by liposome for infecting LNCaP and PC3 cell lines,respectively. The expression level of SMO mRNA,tumor cell proliferation and cell cycle were measured by quantitative realtime polymerase chain reaction (qRT-PCR),3-(4,5)-dimethylthiahiazo (-z-yl)-3,5-di-phenytetrazoliumromide (MTT) assay and flow eytometry,respectively. Sequence results showed that recombinant lentiviral vectors were constructed successfully.pGCSIL-GFP-723 had the highest interfering efficiency,named Lv-SIL-SMO723 after co-transfection,with which LNCaP and PC3 cell lines were infected. Compared with the control groups,results showed significantly decreased (P〈0.05) SMO mRNA expressions of LNCaP and PC3,lower mean percentage of S-phase cells and higher mean percentage of G_2/M phase cells,as well as obviously slow proliferation (P〈0.01) of LNCaP in the infected group. Yet,the proliferation of PC3 was not altered (P〉0.05). In conclusion,the recombinant lentivirus particles were able to suppress SMO expression,regulate the cell cycle in the LNCaP and PC3 cell lines and markedly inhibit proliferation of LNCaP cells but not PC3 cells.
Bo YangHeng-Yun SunWei-Hua ChenJi-Ling WenXiang-Ting ShiYue-Min Wang
关键词:LENTIVIRUSSMOOTHENED
SMO特异性siRNA慢病毒载体的筛选构建被引量:1
2009年
目的构建特异性沉默SMO基因的重组慢病毒载体,筛选对T293细胞SMO基因表达抑制效率最高的siRNA。方法根据SMO基因信息,设计了4个小干扰序列和1个阴性对照序列,利用慢病毒质粒载体pGCSIL-GFP构建了5个重组质粒。用脂质体将重组慢病毒载体转染293T细胞后,Western blot检测沉默效率,从中筛选沉默效率高的质粒载体进行慢病毒颗粒大量包装。结果测序结果证明4个重组慢病毒质粒载体pGCSIL-GFP-721、pGCSIL-GFP-722、pGCSIL-GFP-723、pGCSIL-GFP-724的插入序列完全正确,重组慢病毒载体转染293T细胞后,Western blotting证实重组慢病毒质粒载体pGCSIL-GFP-723的干扰效率最高。包装获得Lv-SIL-SMO723慢病毒颗粒。结论成功筛选获得特异性抑制SMO的siRNA,成功构建了特异性沉默SMO基因慢病毒载体,其产生的慢病毒颗粒能高效特异地沉默SMO基因,为进一步应用奠定基础。
杨波陈卫华温机灵华咏王跃闽
关键词:RNA干扰慢病毒
前列腺肿瘤早期诊断相关标志物的研究进展被引量:1
2011年
随着我国前列腺肿瘤发病率的日益增高,前列腺肿瘤的早期诊断日益受到临床医师的重视。近年来,诊断方法的改进及部分新肿瘤标志物的发现,使早期前列腺肿瘤能被正确诊断并接受合理的治疗。
胡昕海王跃闽
关键词:前列腺肿瘤肿瘤标志物
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