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作 者:吴海峰[1] 李猛[2] 高裕[2] 李广永[1] 陈福宝[1]
机构地区:[1]宁夏医科大学总医院泌尿外科,宁夏银川750004 [2]宁夏医科大学,宁夏银川750004
出 处:《宁夏医学杂志》2016年第1期4-6,共3页Ningxia Medical Journal
摘 要:目的探讨不同浓度磷脂酰肌醇3激酶(PI3K)抑制剂LY294002对人膀胱尿路上皮癌细胞BC-6增殖及凋亡的影响。方法临床采集30例膀胱尿路上皮癌患者的癌组织和癌旁组织,用RT-PCR方法检测其PI3K、Akt、m TOR的表达情况;以终浓度为5、10、20、40μmol/L的LY294002作用于人膀胱尿路上皮癌细胞48 h,以MTT法检测细胞增殖情况,DAPI染色法比较细胞凋亡率,Western blot方法检测Akt和p-Akt的表达变化。结果 RT-PCR法发现膀胱尿路上皮癌组织中PI3K、Akt、m TOR的表达显著高于癌旁组织。不同浓度的LY294002对人膀胱尿路上皮癌细胞均有抑制增殖作用与促进凋亡作用,并呈一定时间和浓度的依赖性。此外,经LY294002处理的BC-6细胞Akt和p-Akt表达量下降且呈一定的剂量依赖性。结论 LY294002通过抑制PI3K-Akt通路对人膀胱尿路上皮癌细胞起抑制增殖和促进凋亡作用。Objective To investigate the effects of different concentrations of phosphoinositide 3 - kinase (PI3K) inhibitor LY294002 on proliferation and apoptosis of human bladder urothelial carcinoma cells ( BC - 6 cells). Methods Specimens of carcinoma and adjacent tissues were collected from 30 patients with bladder urothelial carcinoma for detecting the expression of PI3K/Akt/mTOR by RT -PCR. BC -6 cells were treated with final concentrations of 5 μmol/L, 10 μmol/L,20 μmol/L,40 μmol/L LY294002 for 48 hours, then evaluated the proliferation inhibitory rate by MTr assay; the apoptosis rate was detected by DAPI staining; the protein expression level of phosphorylated - Akt ( p - Akt) and Akt in BC - 6 cells were detected by Western blot. Results RT - PCR assay showed that the expression of PI3K/Akt/mTOR in bladder urothelial carcinoma was significantly higher than that in adjacent tissue. The growth of BC - 6 cells was inhibited by LY294002, and it was in a time and dose - dependent manner. In addition, the expression of Akt and p - Akt decreased and showed a dose dependent treated with LY294002. Conclusion LY294002 could inhibit the proliferation and promotes the apoptosis of human bladder urothelial carcinoma cells by inhibiting the PI3K - Akt pathway.
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