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作 者:顾晓霞[1] 李洁[1] 吴梅红[1] 彭小波[1] 湛先保[1]
机构地区:[1]第二军医大学长海医院肿瘤科,上海200433
出 处:《中华胰腺病杂志》2017年第1期12-14,共3页Chinese Journal of Pancreatology
摘 要:目的探讨阿帕替尼(Apatinib)对体外培养的胰腺癌AsPC-1细胞增殖、凋亡、迁移的影响。方法以不同浓度Apatinib干预胰腺癌AsPC-1细胞,采用CCK-8法和流式细胞技术检测细胞的增殖和凋亡,通过划痕实验观察Apatinib对胰腺癌细胞迁移能力的影响。结果对照组及10、20、30、40、50μmol/L Apatinib处理组AsPC-1细胞的增殖抑制率分别为0、(1.45±0.68)%、(16.92±0.70)%、(23.84±0.84)%、(34.35±1.55)%、(37.33±0.81)%,细胞增殖随Apatinib浓度的增加而显著被抑制,差异有统计学意义(P〈0.05)。对照组及20、40 μmol/L Apatinib处理组AsPC-1细胞的凋亡率分别为(9.44±0.18)%、(16.62±0.19)%、(25.42±0.41)%,细胞凋亡数量随Apatinib浓度增加而显著增多,差异具有统计学意义(P〈0.05)。对照组及20、40 μmol/L Apatinib处理组AsPC-1细胞的迁移率分别为(29.5±0.7)%、(17.4±0.9)%、(6.6±0.5)%,细胞迁移能力随Apatinib浓度增加而显著下降,差异有统计学意义(P〈0.05)。结论Apatinib能有效抑制胰腺癌AsPC-1细胞的增殖、迁移,并诱导其凋亡。Objective To investigate the effect of apatinib on the proliferation, apoptosis and migration of pancreatic cancer cell line AsPC-1 in vitro. Methods Pancreatic cancer AsPC-1 cells were treated by apatinib in different concentrations. Cell proliferation and apoptosis were measured by CCK-8 and flow cytometry, and the effect of apatinib on cell migration ability was observed by wound healing assay. Results In control and 10, 20, 30, 40 and 50umol/L apatinib treatment group, the inhibitory rates of AsPC- 1 cells were0,(1.45±0.68)%,(16.92±0.70)%,(23.84±0.84)%,(34.35±1.55)% and (37.33± 0.81 )% ,respectively. Cell proliferation was obviously inhibited by apatinib as the concentration increased, and the differences were statistically significant ( P 〈 0.05 ). In control and 20, 40 umol/L apatinib treatment group, the apoptotic rates were (9.44 ± 0.18 ) %, ( 16.62 ± 0.19) % and (25.42 ± 0.41 ) %, respectively. Number of apoptotic cells was obviously increased by apatinib as the concentration increased, and the differences were statistically significant (P 〈 0.05 ). In control and 20, 40 umol/L apatinib treatment group, the migration ability was ( 29.5 ± 0.7 ) % , ( 17.4 ± 0.9 ) % and ( 6.6 ± 0.5 ) % , which was greatly decreased as the concentration increased, and the differences were statistically significant (P 〈 0.05 ). Conclusions Apatinib can effectively inhibit the proliferation and migration of pancreatic cancer AsPC-1 cells and induce apoptosis.
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