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作 者:王全玉[1] 何炜[2] 蔺强[1] 李莉蕊[2] 吴振启[3]
机构地区:[1]河北医科大学附属华北石油管理局总医院肿瘤科,河北任丘062550 [2]河北医科大学附属华北石油管理局总医院物理诊断科,河北任062550 [3]湖北医药学院,湖北十堰442000
出 处:《现代肿瘤医学》2015年第13期1855-1858,共4页Journal of Modern Oncology
基 金:湖北省卫生厅科研基金(编号:JX3B27)
摘 要:目的:探讨膀胱癌组织中DNMT蛋白表达水平与肿瘤增殖和凋亡程度的相关性。方法:收集膀胱癌组织标本80例和正常膀胱组织标本80例进行DNMT蛋白免疫组化分析。同时选择ABS-1膀胱癌细胞分为空白组、对照组、实验组。空白组加入常规培养基,对照组转染50nmol/L的空载体,实验组转染50nmol/L DNMT1 siRNA载体,然后进行肿瘤的增殖与凋亡分析。收集细胞进行DNMT蛋白表达检测。结果:DNMT1蛋白在膀胱癌组织中的阳性表达率为42.5%,在正常膀胱组织中的阳性表达率为2.5%,对比差异明显(P<0.05)。转染后DNMT1在空白组、对照组、实验组中的相对表达量分别为0.512±0.014、0.485±0.037和0.100±0.034,对比差异明显(P<0.05)。实验组增殖性明显低于空白组和对照组,而细胞凋亡率明显高于空白组和对照组,组间对比差异均有统计学意义(P<0.05)。结论:膀胱癌组织与膀胱癌细胞中存在DNMT1蛋白过表达,抑制DNMT1蛋白表达能有效抑制肿瘤细胞的增殖和促进凋亡。Objective:To investigate the correlation of DNMT Protein exPression levels and tumor Proliferation and aPoPtosis in the bladder carcinoma. Methods:All 80 bladder tissue samPles and 80 normal bladder tissue samPles were collected for DNMT Protein immunohistochemical analysis. Selected ABS-1 bladder cancer cell line were divid-ed into the blank grouP,control grouP,exPerimental grouP,blank grouP were give the regular medium,control grouP were transfected with 50nmol/L of air carriers,exPerimental grouP were transfected with 50nmol/L DNMT1 siRNA vectors,then the tumor Proliferation and aPoPtosis were analyzed. Also collected cells for DNMT Protein detection. Re-sults:The DNMT1 Protein Positive exPression in bladder cancer tissues were 42. 5%,2. 5% in normal bladder tissue (P〈0. 05). After transfection,the DNMT1 relative exPression amount in the blank grouP,the control grouP,the ex-PerimentalgrouPwere0.512±0.014,0.485±0.037and0.100±0.034(P〈0.05).TheProliferativeratesinthe exPerimental grouP was significantly lower than the blank grouP and the control grouP,while the aPoPtosis rate was significantly higher than the blank grouP and the control grouP(P〈0. 05). Conclusion:The DNMT1 Protein exPres-sion in the bladder cancer tissue and cells were higher,inhibition of DNMT1 Protein can inhibit tumor cell Prolifera-tion and induce aPoPtosis.
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