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机构地区:[1]盘锦市中心医院肿瘤4科,辽宁省盘锦124000 [2]山东大学附属省立医院肿瘤研究所 [3]盘锦市中心医院普通外4科 [4]山东大学附属省立医院胸外科
出 处:《中国医师杂志》2013年第9期1195-1198,共4页Journal of Chinese Physician
摘 要:目的探讨JAK/STAT3信号转导途径对肝癌细胞凋亡的影响。方法以BEL-7402肝癌细胞为模型,采用RNAi技术,将STAT3-siRNA转染BEL-7402肝癌细胞,沉默STAT3基因表达,另设细胞对照组,阴性质粒组(pGCsi.U6/neoRFPscramble-siRNA载体转染BEL-7402)。分别通过流式细胞术检测细胞凋亡比率的变化,JC-1荧光染色观察线粒体膜电势AW。变化,并利用WesternBlot方法检测Caspase3蛋白质水平的变化。结果STAT3-siRNA组凋亡率为(38.82±0.88)%,明显高于其他组[对照组(9.22±0.38)%,阴性质粒组(16.47±1.04)%,P〈0.05],并引起细胞线粒体膜电势明显降低[(59.06±1.89)%vs(91.33±1.78)%和(89.90±1.92)%,P〈0.05],活性Caspase3蛋白在STAT3-siRNA组表达明显高于其他组(0.48±0.05VS0.22±0.04和0.26±0.06,P〈0.05)。结论RNAi沉默STAT3基因,抑制JAK/STAT3信号转导途径,促进BEL-7402肝癌细胞凋亡。Objective To explore influence of JAK/STAT3 signaling pathway on the apoptosis .of HCC cells. Methods DNA-vector-based RNAi approach silence was used to down-regnlate STAT3 expres- sion in Bel-7402 cells. According to the STAT3 cDNA sequence in the GeneBank database, the plasmid pGCsi. U6/neoRFP -STAT3 that was designed for expression of STAT3 siRNA was constructed and synthe- sized, and then transfected into the Bel-7402 cells with lipofectamine 2000. The apoptotic rate was meas- ured with flow cytometry (FCM) and annexinV/PI apoptosis detection kit staining. The mitochondrial mem- brane potential (B^m) was visualized by the JC-1 fluorescence staining and the inverted fluorescence mi- croscope. Moreover, the expression of caspase-3 protein was analyzed by Western blotting. Results The apoptotie ratio of STAT3-siRNA group was ( 38. 82 ± 0. 88 ) % , which was significantly higher than that in other group [ control group(9. 22 ± 0. 38 ) %, scramble-siRNA group( 16.47± 1. 04 ) %, P 〈 0.05 ]. The mitochondrial membrane potential of STAT3-siRNA group observed by the JC-1 fluorescence staining was decreased significantly[ (91.33±1.78 ) % ] and [ ( 89.90 ± 1.92 ) % vs ( 59.06 ±1.89 ) %, P 〈 0. 05 ]. The Western blot results showed that the protein expression of active caspase-3 in STAT3-siRNA group was significantly higher than other groups ( 0. 48± 0. 05 vs 0. 22 ±0. 04 and 0. 26 ±0. 06, P 〈 0. 05 ). Conclu- sions STAT3 gene silencing significantly improves the apoptotic effect in the Bel-7402 cells.
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