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帕纳替尼调控miR-92b-3p对胆管癌恶性生物学行为的影响

邱实 杜杰 罗刚 林一煌 张子强 江帆

中国临床药理学杂志2024,Vol.40Issue(19):2847-2852,6.
中国临床药理学杂志2024,Vol.40Issue(19):2847-2852,6.DOI:10.13699/j.cnki.1001-6821.2024.19.018

帕纳替尼调控miR-92b-3p对胆管癌恶性生物学行为的影响

Effects of panatinib regulation of miR-92b-3p on malignant biological behavior of cholangiocarcinoma

邱实 1杜杰 2罗刚 2林一煌 1张子强 1江帆1

作者信息

  • 1. 武汉市普仁医院胆石病中心,湖北武汉 430080
  • 2. 武汉市普仁医院肝胆胰疝外科,湖北武汉 430080
  • 折叠

摘要

Abstract

Objective To study the effect of panatinib on cholangiocarcinoma(CCA)and its molecular mechanism.Methods QBC939 cells were divided into control group(no treatment),low dose group(0.1 μmol·L-1 panatinib treatment),medium dose group(0.5μmol·L-1panatinib treatment),high dose group(1.0 μmol·L-1 panatinib treatment)and high dose+microRNA-92b-3 group(after treatment with 1.0 μmol·L-1 panatinib transfected miR-92b-3p mimic),high-dose+miR-92b-3p mimic+overexpressed homologous domain interacting protein kinase 3 plasmid(oe-HIPK3)group(after treatment with 1.0 μmol·L-1 panatinib,miR-92b-3p mimic and oe-HIPK3),mimic-NC group(transfected miR-92b-3p NC),and miR-92b-3p mimic group(transfected miR-92b-3p mimic)were transfected.Cell proliferation was detected by cell counting kit 8(CCK-8);cell migration was detected by Transwell,the relative expression level of protein was detected by Western blot.Results Cell proliferation rates of control group,high-dose group,high-dose+miR-92b-3p mimic group,and high-dose+miR-92b-3p mimic group mimic+oe-HIPK3 group were(76.58±8.56)%,(61.85±7.77)%,(74.54±7.68)%and(58.63±6.87)%,respectively;the number of cells migrated were 185.32±20.14,132.33±18.99,168.23±19.85 and 138.66±15.95,respectively;phosphorylated phosphatidyl inositide 3-kinase(p-PI3K)/PI3K ratios were 1.00±0.23,0.68±0.09,0.91±0.18 and 0.60±0.08,respectively;phosphorylated protein kinase B(p-AKT)/AKT ratios were 1.00±0.25,0.61±0.08,1.12±0.28 and 0.72±0.14,respectively.The above indexes were compared with those of the control group in the high-dose group,and those of the high-dose+miR-92b-3p mimic group in the high-dose+miR-92b-3p mimic group in the oe-HIPK3 group.There were statistically significant differences(all P<0.05).Conclusion Panatinib can effectively inhibit the evil biological behavior of cholangiocarcinoma,which may be related to inhibiting the level of miR-92b-3p and promoting HIPK3-mediated PI3K/AKT signaling pathway.

关键词

帕纳替尼/非编码微小RNA-92b-3p/胆管癌/同源结构域相互作用蛋白激酶3/磷脂酰肌醇3-激酶/蛋白激酶B信号通路

Key words

ponatinib/microRNA-92b-3p/cholangiocarcinoma/homeodomain interacting protein kinase 3/phosphatidyl inositide 3-kinase/protein kinase B signaling pathway

分类

医药卫生

引用本文复制引用

邱实,杜杰,罗刚,林一煌,张子强,江帆..帕纳替尼调控miR-92b-3p对胆管癌恶性生物学行为的影响[J].中国临床药理学杂志,2024,40(19):2847-2852,6.

中国临床药理学杂志

OA北大核心CSTPCD

1001-6821

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