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作 者:周俊蛟[1,2,3] 聂敏海[1,2] 雷波[1,2] 伍宝琴[1,2]
机构地区:[1]泸州医学院附属口腔医院口腔内科 [2]泸州医学院口颌面修复和再生实验室,四川泸州646000 [3]重庆市沙坪坝区人民医院口腔科
出 处:《临床口腔医学杂志》2015年第10期595-598,共4页Journal of Clinical Stomatology
基 金:泸州市科技局科研项目[2013-S-50(3/3)]
摘 要:目的:研究4-氨基吡啶(4-AP)对人舌鳞状细胞癌(OTSCC)Tca8113细胞体外迁徙和侵袭能力的影响。方法:采用划痕愈合方法及Transwell侵袭实验检测10、20、30 mmol/L 4-AP干预Tca8113细胞后对Tca8113细胞迁徙及侵袭能力的影响。结果:浓度分别为10 mmol/L、20 mmol/L、30 mmol/L 4-AP干预Tca8113细胞后,Tca8113细胞12 h迁徙率分别为(14.07±5.59)%、(11.34±1.79)%及(8.71±3.26)%;24 h的迁徙率分别为(22.20±5.30)%、(14.24±2.52)%及(11.65±2.97)%,均明显小于对照组(19.25±4.50)%和(33.16±6.40)%,差异具有显著性(P<0.01)。细胞侵袭实验结果显示,10 mmol/L、20 mmol/L、30 mmol/L的4-AP作用于Tca8113细胞24 h后穿膜细胞数分别为(112.20±24.36)、(28.87±6.47)、(11.80±5.77)个,随着4-AP浓度的升高,Tca8113穿膜细胞数明显下降,与对照组(179.73±16.14)相比,差异具有显著性(P<0.001)。结论:4-AP具有抑制Tca8113舌鳞癌细胞株体外迁徙侵袭的能力。Objective:To explore the effect of 4-AP on the migration and invasion of Tca8113 cells, thus provide reference for clinical studies. Method: Wound healing assay and Transwell assay were employed to explore whether 4-AP (10, 20, 30 mmol / ID could inhibit the migration and invasion of Tca8113 cell. Result: ①The scratch healing assay obtained cell migration rates of (19.25±4.50) %, (14.07±5.59) %, (11.34±1.79) % and (8.71 ±3.26) % for Tca8113 cells treated with 10, 20, 30 mmol / L of 4-AP for 12 h while (33.16±6.40)%, (22.20±5.30)%, (14.24±2.52)% and (11.65±2.97)% for 24 h. The results showed that the migration rates were significantly difference between 4-AP goups (10, 20, 30 mmol/L)and control groups (P 〈0.01).②The transwell invasion assay showed that with the increasing of 4-AP concentration, the Tca8113 cell number decrased. The number of cells permeating through the matrigel were (112.20±24.36), (28.87±6.47), (11.80±5.77) when the Tca8113 cells were treated with 10 mmol / L,20 mmol / L, 30 mmol / L 4-AP for 24 h,while the control group was (179.73±16.14),and the difference was significant (F =392.045, P 〈0.001). Conclusion:4-AP can significantly inhibited the migration and invasion of human tongue carcinoma cell line Tca8113.
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