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作 者:吴迪[1,2] 田小强[1,2] 蔡云朗[1,2] 常立功[1,2] 余丹丹[1,2] 沈杨[1,2] 任慕兰[1,2] 黄培林[1,2]
机构地区:[1]东南大学医学院 [2]东南大学附属中大医院妇产科,江苏省210009
出 处:《江苏医药》2014年第10期1123-1126,共4页Jiangsu Medical Journal
摘 要:目的探讨PI-103对卵巢癌恶性表型的调控及其对卵巢癌脂肪酸合酶(FASN)表达的影响。方法 Western blot检测卵巢癌细胞株A2780,SKOV3/DDP和SKOV3中FASN的表达(对照组);将FASN表达量最高的细胞株A2780用药物PI-103处理(实验组)。采用MTT测定细胞抑制率、平板克隆形成实验和Transwell小室实验比较实验组与对照组的细胞生物学特性,Western blot比较两组细胞的FASN、p-Akt和p-rpS6表达。结果随着时间的延长,实验组的细胞增殖能力较对照组减弱(P<0.05)、克隆形成率降低[(8.45±1.04)%vs.(15.40±0.82)%](P<0.05)、侵袭细胞数减少[(58.67±6.51)个vs.(156.33±4.04)个](P<0.05)。实验组FASN、p-Akt和p-rpS6的蛋白表达水平均低于对照组(P<0.05)。结论 PI-103可有效抑制卵巢癌A2780细胞的PI3K/AKT/mTOR信号通路中相关蛋白的表达;在体外显著抑制细胞的增殖和侵袭。Objective To explore the effect of PI-103 on ovarian malignant phenotype and fatty acid synthase(FASN) expression. Methods The expression of FASN in ovarian cancer cell lines A2780,SKOV3/DDP and SKOV3 was detected by Western blot(group B, as the control), of which A2780 was with the highest expression level of FASN and treated with PI-103 (group A). The biological characteristics detected by MTT, plate clone formation assay and Transwell assay were compared between two groups. The expressions of p-Akt, p-rpS6 and FASN proteins in the PI3K/ mTOR pathway were detected by Western blot and compared between two groups as well. Results Compared with A2780 cells in group B, as time went on, PI-103 significantly inhibited the growth of those in group A, with decreased viability, colon formation rate[(8. 45 ±1.04)% vs. (15. 40 ±0. 82)%] (P〈0.05), and the number of cells travelling through the matrigel [(58. 67±6.51) pieces vs. (156. 33±4. 04) pieces](P〈0. 05). Compared with group B, PI-103 significantly down-regulated the expressions of p-Akt, p-rpS6 and FASN in group A(P〈0. 05). Conclusion PI-103 significantly inhibits the PI3K/AKT/mTOR signaling pathway and effectively down-regulates relative protein expression and in vivo inhibits proliferation and invasion of ovarian cancer A2780 cells.
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