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Combined transfection of Bcl-2 siRNA and miR-15a oligonucleotides enhanced methotrexate-induced apoptosis in Raji cells 被引量:1
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作者 Li Ding Xiao-Mao Hu +4 位作者 Hong Wu Ge-Xiu Liu Yang-Jun Gao Dong-Mei He Yuan Zhang 《Cancer Biology & Medicine》 SCIE CAS CSCD 2013年第1期16-21,共6页
Objective: B-cell lymphoma 2 (Bcl-2) is an important member of the Bcl-2 family of proteins that regulate the induction of apoptosis. This study aims to investigate whether Bcl-2 small interfering RNA (siRNA) combined... Objective: B-cell lymphoma 2 (Bcl-2) is an important member of the Bcl-2 family of proteins that regulate the induction of apoptosis. This study aims to investigate whether Bcl-2 small interfering RNA (siRNA) combined with miR-15a oligonucleotides (ODN) could enhance methotrexate (MTX)-induced apoptosis in Raji cells. Methods: Chemically synthesized miR-15a ODN and Bcl-2 siRNA were transfected in Raji cells by using a HiPerFect Transfection Reagent and then combined with MTX. Expression levels of Bcl-2 protein were detected by Western blot. Cell proliferation was determined by CCK8 assay. The rate of cell apoptosis was determined by Annexin V/PI double staining. The morphology of apoptotic cells was observed by Hoechst-33 258 staining. Results: After the cells were transfected with miR-15a ODN combined with Bcl-2 siRNA, Bcl-2 protein levels were evidently decreased. CCK8 assay showed that cell proliferation was significantly decreased and was significantly lower in miR-15a ODN combined with Bcl-2 siRNA plus MTX group than in miR-15a ODN with methotrexate group, Bcl- 2 siRNA with MTX group, and single MTX group (P<0.05). Hoechst 33258 staining revealed numerous apoptotic cells. AnnexinV/PI double staining showed that the apoptotic rates were (13.13±1.60)%, (34.47±2.96)%, (32.87±3.48)%, and (45.47±2.16)% in MTX, Bcl-2 siRNA plus MTX, miR-15a ODN plus MTX, and miR-15a ODN combined with Bcl- 2 siRNA plus MTX groups, respectively. Among these groups, the apoptotic rate of miR-15a ODN combined with Bcl-2 siRNA plus MTX group was the highest; this apoptotic rate was also significantly different from that of miR-15a ODN or Bcl-2 siRNA plus MTX (P<0.05). Conclusions: Bcl-2 siRNA combined with miR-15a ODN could enhance MTX-induced apoptosis in Raji cells. Bcl-2 siRNA and miR-15a combined with MTX may be a useful approach to improve the treatment effects on lymphoma. 展开更多
关键词 B-cell lymphoma 2 bcl-2 small interfering RNA OLIGONUCLEOTIDE METHOTREXATE Raji cell miR-15a apoptosis
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氯沙坦在损伤血管重构中的作用及其机制的探讨 被引量:7
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作者 杨彬 成蓓 +3 位作者 刘承云 张湖萍 江凌 陈学林 《心脏杂志》 CAS 2004年第1期23-25,28,共4页
目的 ::探讨氯沙坦在大鼠血管内膜剥脱术后血管重塑中的作用及其内在机制。方法 :将 Wistar大鼠随机分为假手术组、氯沙坦组及单纯 PTCA组。后两组大鼠行胸主动脉球囊损伤术 ,术后不同时间段处死。对主动脉的组织切片分别进行 HE染色及... 目的 ::探讨氯沙坦在大鼠血管内膜剥脱术后血管重塑中的作用及其内在机制。方法 :将 Wistar大鼠随机分为假手术组、氯沙坦组及单纯 PTCA组。后两组大鼠行胸主动脉球囊损伤术 ,术后不同时间段处死。对主动脉的组织切片分别进行 HE染色及计算机图像分析、Tunel标记检测细胞凋亡率、免疫组化方法检测血管壁凋亡相关基因表达物 Fas、Fas-L、Bcl-2、Bax的变化。结果 :单纯 PTCA组术后 7、14 d管壁面积明显增加 ,与假手术组比较有显著性差异 (P<0 .0 5)。术后 14 d,氯沙坦组与单纯 PTCA组比较 ,管壁增生程度较轻。术后 7d,管壁面积增生比与细胞凋亡率之间有负相关性 (r=-0 .586,P<0 .0 5) ,氯沙坦组的细胞凋亡率显著高于单纯 PTCA组。氯沙坦组与单纯PTCA组比较 ,术后 7d管壁组织内 Fas-L表达增加 ,Bcl-2表达降低 (P<0 .0 5)。结论 :AT1受体拮抗剂氯沙坦可有效防止大鼠动脉损伤后的血管增生性重塑。其机制可能与促进 Fas的表达、抑制 Bcl-2的表达 。 展开更多
关键词 氯沙坦 细胞凋亡 术后再狭窄 bcl-2蛋白族
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