文章摘要
李雪玲,张凯敏,李娈英,等.白藜芦醇联合SB203580对宫颈癌细胞凋亡迁移的影响及机制[J].安徽医药,2019,23(2):240-245.
白藜芦醇联合SB203580对宫颈癌细胞凋亡迁移的影响及机制
Effect and mechanism of resveratrol combined with SB203580 on the apoptosis and migration of cervical cancer cells
投稿时间:2016-10-17  
DOI:
中文关键词: 白藜芦醇  p38  SB203580  宫颈癌  凋亡  迁移
英文关键词: Resveratrol  p38  SB203580  Cervical cancer  Apoptosis  Migration
基金项目:河南省医学科技攻关计划项目(122300410036) ◇药学研究◇白藜芦醇联合SB203580对宫颈癌细胞凋亡迁移的影响及机制 李雪玲1,张凯敏1,李娈英1,李明君2(1.漯河市第三人民医院妇产科,河南 漯河 462000;2.郑州大学第一附属医院肿瘤科,河南 郑州 450052)
作者单位
李雪玲 漯河市第三人民医院妇产科,河南 漯河 462000 
张凯敏 漯河市第三人民医院妇产科,河南 漯河 462000 
李娈英 漯河市第三人民医院妇产科,河南 漯河 462000 
李明君 郑州大学第一附属医院肿瘤科,河南 郑州 450052 
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中文摘要:
      目的 探讨白藜芦醇联合SB203580对宫颈癌细胞凋亡迁移的影响及机制。方法 培养人宫颈癌HeLa细胞,CCK8实验检测不同浓度白藜芦醇作用于细胞48 h后对细胞增殖影响,挑选最佳作用浓度。将细胞分为四组,即对照组(A组):不做处理;SB203580组(B组),加10 μmol/L SB203580;白藜芦醇组(C组),加60 μmol/L白藜芦醇;白藜芦醇组+SB203580组(D组),加60 μmol/L白藜芦醇和10 μmol/L SB203580。流式细胞仪、Transwell小室检测四组细胞的凋亡率和迁移数,Western blot检测p38、p-p38、活化的含半胱氨酸的天冬氨酸蛋白水解酶3(Cleaved-caspase3)、B型白细胞/2型淋巴细胞样蛋白(Bcl-2)、Bcl-2相关X蛋白(Bax)蛋白表达。结果 白藜芦醇能显著抑制人宫颈癌HeLa细胞增殖,60 μmol/L白藜芦醇抑制了一半的细胞增殖(P<0.001);B组(14.83±1.23)%细胞凋亡率显著低于A组(3.42±0.78)%,细胞迁移数(189.20±7.93)显著高于A组(135.40±7.23);C组(35.57±1.86)%和D组(23.45±1.45)%细胞凋亡率显著高于A组,C组(51.30±5.49)和D组(97.60±6.88)细胞迁移数显著低于A组;D组细胞凋亡率显著高于B组,低于C组,细胞迁移数显著低于B组,高于C组(P<0.001);B组p-p38[(0.087±0.011比0.152±0.014)]、Cleaved-caspase3 [(0.162±0.011比0.093±0.009)]、Bax蛋白表达[(0.191±0.013)比(0.154±0.012)]显著低于A组,Bcl-2蛋白表达[(0.208±0.014)比(0.347±0.015)]显著高于A组;C组和D组p-p38[(0.282±0.016)、(0.201±0.015)]、Cleaved-caspase3[(0.315±0.013)、(0.223±0.012)]、Bax蛋白表达[(0.441±0.015)、(0.294±0.014)]显著高于A组,C组和D组Bcl-2蛋白表达[(0.071±0.010)、(0.156±0.012)]显著低于A组;D组p-p38、Cleaved-caspase3、Bax蛋白表达显著高于B组,低于C组,Bcl-2蛋白表达显著低于B组,高于C组(P<0.001)。p38蛋白表达在各组之间差异无统计学意义(P>0.05)。结论 白藜芦醇通过调控p38MAPK信号通路抑制人宫颈癌HeLa细胞增殖和迁移,并通过调节Cleaved-caspase3、Bax、Bcl-2促进细胞凋亡。
英文摘要:
      Objective To investigate the effect and mechanism of resveratrol combined with SB203580 on the apoptosis and migration of cervical cancer cells.Methods Human cervical carcinoma HeLa cells were cultured,and the effect of different concentrations of resveratrol on cell proliferation was detected by CCK8 assay,and optimal concentration was selected.The cells were assigned into four groups:control group (group A),no treatment;SB203580 group (group B),with 10 μmol/L SB203580;resveratrol group (group C),with 60 μmol/L resveratrol;resveratrol and SB203580 group (group D),with 60 μmol/L resveratrol and 10 μmol/L SB203580.Cell apoptosis and migration number were detected in four groups by flow cytometry and Transwell assay separately;expressions of p38,p-p38,Cleaved cysteinyl aspartate specific proteinase 3 (Cleaved-caspase 3),B-cell leukemia/lymphoma 2-like proteins (Bcl-2),Bcl-2 associated Xprotein (Bax) was detected by Western blot.Results Resveratrol could significantly inhibit the proliferation of human cervical carcinoma HeLa cells,60 μmol/L resveratrol inhibited half cell proliferation (P<0.001).Apoptosis rate (14.83±1.23)% in group Bwas significantly lower than (3.42±0.78)% of group A,the number of cell migration (189.20±7.93) was significantly higher than (135.40±7.23) of group A.Apoptosis rates in group C (35.57±1.86)% and group D (23.45±1.45)% were significantly higher than group A.Cell migration numbers in group C (51.30±5.49) and group D (97.60±6.88) were significantly lower than group A.The apoptosis rate in group Dwas significantly higher than group B,and lower than group C,and its number of cell migration was significantly lower than group B,and higher than group C (P<0.001).The expressions of Cleaved-Caspase 3,Bax protein and p-p38 in group Bwere significantly lower than group A [(0.162±0.011) vs. (0.093±0.009),(0.191±0.013) vs. (0.154±0.012),(0.087±0.011) vs. (0.152±0.014),respectively],and the expression of Bcl-2 protein was significantly higher than group A [(0.208±0.014) vs.(0.347±0.015)].The expressions of p-p38,Cleaved-caspase 3,Bax protein in group C [(0.282±0.016),(0.315±0.013) and (0.441±0.015),respectively] and group D [(0.201±0.015),(0.223±0.012) and (0.294±0.014),respectively] were significantly higher than group A,and the expressions of Bcl-2 protein in group C (0.071±0.010) and group D (0.156±0.012) were significantly lower than group A.The expressions of p-p38,Cleaved-caspase 3,Bax protein in group Dwere significantly higher than group B,but lower than group C.The expression of Bcl-2 protein in group Dwas significantly lower than group B,but higher than group C (P<0.001).There was no significant difference in p38 protein expression among the groups (P>0.05).Conclusions Resveratrol can inhibit the proliferation and migration of human cervical cancer HeLa cells through regulating the p38MAPK signaling pathway,and promote cell apoptosis through regulation of Cleaved-caspase 3,Bax and Bcl-2.
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