首页|奥美拉唑抑制miR-214-3p介导自噬提高上皮性卵巢癌细胞对顺铂的敏感性

奥美拉唑抑制miR-214-3p介导自噬提高上皮性卵巢癌细胞对顺铂的敏感性

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目的 探讨奥美拉唑(omeprazole,OME)能否通过抑制自噬提高人卵巢上皮性癌(卵巢癌,EOC)细胞对顺铂的敏感性及其可能机制。方法 原位杂交及免疫组化检测卵巢癌组织中miR-214-3p及自噬标记物p62表达;Pearson相关分析探讨R-214-3p和p62在EOC组织中表达量的相关性;CCK-8法检测各组细胞顺铂半数抑制浓度(IC50);实时定量PCR(qRT-PCR)分析miR-214-3p及多药耐药基因-1(MDR1)表达;蛋白质印迹法检测p62及耐药蛋白p-gp表达。结果 在43例卵巢癌患者的样本中,23例(53。5%)miR-214-3p表达阳性,26例(60。5%)p62表达阳性,miR-214-3p在铂相对耐药EOC中表达低于铂敏感EOC(P<0。05);相反,p62在铂相对耐药EOC中表达明显高于铂敏感EOC(P<0。01)。miR-214-3p 和 p62 在卵巢癌中表达呈负相关(r=-0。387,P=0。005);OME(150 μmol/L)预处理后,OV2008 及C13K细胞对顺铂IC5。均有不同程度降低,尤以顺铂耐药株C13K更为显著(P<0。01)。与空白对照组C13K及OV2008细胞比较,顺铂作用后,C13K及OV2008细胞中miR-214-3p相对表达下降,MDR1基因在mRNA及蛋白水平表达均升高,p62蛋白表达升高(均P<0。01);相反,OME(150μmol/L)预处理可使C13K及OV2008细胞对顺铂敏感性增加,细胞中miR-214-3p相对表达明显升高、MDR1在蛋白及mRNA水平表达降低、p62蛋白表达下降(均P<0。05)。结论 OME预处理可提高卵巢癌细胞对顺铂敏感性,其机制与抑制miR-214-3p介导的自噬有关。
Omeprazole Enhances Cisplatin Sensitivity Through Inhibition of miR-214-3p Mediated Autophagy in Epithelial Ovarian Cancer Cells
Objective To investigate whether omeprazole(OME)can enhance the sensitivity of epithelial ovarian cancer(EOC)cells to cisplatin(DDP)by inhibition of autophagy and to elucidate its possible mechanism.Methods Color in situ hy-bridization(CISH)and immunohistochemistry were applied to detect the expression of miR-214-3p and autophagy specific mark-ers p62 in EOC tissues,respectively.Pearson analysis showed the correlation between miR-214-3p and p62 expression levels in EOC.The half concentration(IC50)of DDP was determined by CCK-8 method.The mRNA expressions of miR-214-3p and multi-drug resistance gene 1(MDR1),the protein levels of p-gp and p62 were measured by using real-time quantitative PCR(qRT-PCR)and Western blot,respectively.Results In 43 cases,the expressions of miR-214-3p and p62 were 53.5%(23/43)and 60.5%(26/43)in patients with ovarian carcinoma,respectively.miR-214-3p was downregulated in platinum-relatively resistant OC tissue(P<0.05).On the contrary,p62 was upregulated in platinum-relatively resistant OC tissue(P<0.01).In ovarian cancer,the negative expression of miR-214-3p was closely related with p62(r=0.238,P<0.05).After OME(150 μmol/L)pre-treatment,varying degrees of decrease was observed in cisplatin IC50 OV2008 and C13K cells,especially cisplatin resistant strain C13K(P<0.01).After DDP treatment,qRT-PCR results revealed that the expression of miR-214-3p was decreased,the mRNA and protein expressions of MDR1 were greatly increased,and the protein levels of p62 were increased in C13K and OV2008 cells,compared to the blank control C13K and OV2008 cells(all P<0.01).Compared with the blank control C13K and OV2008 cells,the IC50 of DDP was decreased after pretreatment with OME(150 μmol/L).The sensitivity of C13K and OV2008 cells to DDP was increased after OME(150 μmol/L)pretreatment,the relative expression of miR-214-3p was significantly increased,the expression of MDR1 protein and mRNA was decreased,and the expression of p62 protein was decreased(all P<0.05).Conclu-sion OME pretreatment might enhance the sensitivity of ovarian cancer cells to DDP by downregulating miR-214-3p mediated autophagy.

miR-214-3pautophagyomeprazoleovarian cancercisplatin resistant

蔡文、季维雪、肖兰、江飞云、陈文刚、陶云松

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华东师范大学附属芜湖医院(芜湖市第二人民医院)妇科,芜湖 241001

中国科学技术大学附属第一医院妇产科,合肥 230022

皖南医学院第二附属医院药剂科,芜湖 241001

华东师范大学附属芜湖医院(芜湖市第二人民医院)药剂科,芜湖 241001

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miR-214-3p 自噬 奥美拉唑 卵巢癌 顺铂耐药

安徽省卫生健康委员会科研项目

AHWJ2022a028

2024

华中科技大学学报(医学版)
华中科技大学

华中科技大学学报(医学版)

CSTPCD北大核心
影响因子:1.443
ISSN:1672-0741
年,卷(期):2024.53(1)
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