Experimental study on the effect of midazolam on the proliferation and apoptosis of cervical cancer CaSki cells by down-regulating the expression of circ_0000285
ZHANG Jiangchuan, WU Dan, JIANG Wei, ZHANG Chunmei
Department of Anesthesiology,Guang 'an People's Hospital,Guang'an 638000,China
Abstract:ObjectiveTo explore the effect and possible mechanism of midazolam on the proliferation and apoptosis of cervical cancer CaSki cells.MethodsCaSki cells were intervened with different doses(0,15,30,60 μg/mL)of midazolam,and the cell proliferation activity and apoptosis were measured by CCK-8 method and flow cytometry,respectively. The protein expressions of pro-caspase3 and cleaved-caspase3 were determined by western blotting,and the expression of circ_0000285 was determined by RT-qPCR. After CaSki cells that interfered with circ_0000285 expression or overexpressed circ_0000285 were constructed by transfecting circ_0000285 small interfering RNA or overexpression vector,they were intervened with 0 or 60 μg/mL midazolam,and then the same method sas above were used to measure cell proliferation activity,apoptosis and the expression of related proteins(Ki-67,pro-caspase3,cleaved-caspase3).ResultsAfter CaSki cells were intervened by midazolam,the proliferation activity and the protein expressions of Ki-67 and pro-caspase3 were decreased,but the apoptosis rate and the protein expressions of cleaved-caspase3 were increased,and the expression of circ_0000285 in the cells was decreased. After interfering the expression of circ_0000285,the proliferation activity and the protein expressions of Ki-67 and pro-caspase3 in CaSki cells were decreased,but the apoptosis rate and the protein expressions of cleaved-caspase3 were increased. Overexpression of circ_0000285 reversed the effects of midazolam on the proliferation and apoptosis of CaSki cells.ConclusionMidazolam may inhibit the proliferation of cervical cancer CaSki cells and promote cell apoptosis by down-regulating circ_0000285.
张江川, 吴丹, 蒋伟, 张春梅. 咪达唑仑通过下调circ_0000285表达影响宫颈癌CaSki细胞增殖和凋亡的实验研究[J]. 金宝搏官方188学报(医学版), 2023, 20(5): 38-43. ZHANG Jiangchuan, WU Dan, JIANG Wei, ZHANG Chunmei. Experimental study on the effect of midazolam on the proliferation and apoptosis of cervical cancer CaSki cells by down-regulating the expression of circ_0000285. HuNan ShiFan DaXue XueBao(YiXueBan), 2023, 20(5): 38-43.
[1] Wang X,Li TZ.Ropivacaine inhibits the proliferation and migration of colorectal cancer cells through ITGB1[J]. Bioengineered,2021,12(1):44-53. [2] 赵利芳,杨建功. 不同剂量咪达唑仑通过上调miR-33a-5p抑制胶质瘤细胞的增殖,凋亡[J]. 中国老年学杂志,2021,41(20):4520-4525. [3] Sun TT,Chen J,Sun XC,et al.Midazolam increases cisplatin-sensitivity in non-small cell lung cancer(NSCLC)via the miR-194-5p/HOOK3 axis[J]. Cancer Cell Int,2021,21(1):401-411. [4] Oshima Y,Sano M,Kajiwara I,et al.Midazolam exhibits antitumour and anti-inflammatory effects in a mouse model of pancreatic ductal adenocarcinoma[J]. Br J Anaesth,2022,128(4):679-690. [5] 庞旭姣,魏杏茹. circ_0000285通过miR-637/STAT3轴调控宫颈癌细胞的增殖、迁移和侵袭[J]. 广西医科大学学报,2021,38(1): 96-101. [6] 王建东,孔为民,姜昊. 国际妇产科联盟2018年宫颈癌分期及有关问题[J]. 中华肿瘤杂志,2020,42(2):94-98. [7] 黄佳,潘玫,汪利群,等. 丙泊酚抑制wnt/β-catenin通路对宫颈癌HELA细胞生长和运动能力的调节作用[J]. 中国免疫学杂志,2020,36(23):2861-2865+2871. [8] 陈丽娟,张宏,张健,等. 罗哌卡因调控PI3K/Akt信号通路影响宫颈癌细胞HeLa的生物学行为[J]. 中国计划生育和妇产科,2021,13(11):48-51+65. [9] Jiao J H,Wang Y H,Sun X F,et al.Midazolam induces A549 cell apoptosis in vitro via the miR-520d-5p/STAT3 pathway[J]. Int J Clin Exp Pathol,2018,11(3):1365-1373. [10] Lu HL,Wu KC,Chen CW,et al.Anticancer effects of midazolam on lung and breast cancers by inhibiting cell proliferation and epithelial-mesenchymal transition[J]. Life(Basel),2021,11(12):1396. [11] 潘家浩,李强,陈东泰,等. 咪达唑仑对人肝癌细胞增殖能力的影响[J]. 广东医学,2018,39(19):2861-2864. [12] Røge R,Nielsen S,Riber-Hansen R,et al.Ki-67 proliferation index in breast cancer as a function of assessment method:A NordiQC experience[J]. Appl Immunohistochem Mol Morphol,2021,29(2):99-104. [13] Xia GL,Wang AX,Li LX. hsa_circ_0000218/hsa-miR-139-3p/SOX4 regulatory feedback circuit influences the proliferation and apoptosis of gastric cancer cells[J]. Cytotechnology,2022,74(1):89-98. [14] Ji H,Hu NJ.Circular RNA 0001823 aggravates the growth and metastasis of the cervical cancer cells through modulating the microRNA-613/RAB8A axis[J]. Bioengineered,2022,13(4):10335-10349. [15] Ma Y,Liu J,Yang Z,et al.CircRNA_400029 promotes the aggressive behaviors of cervical cancer by regulation of miR-1285-3p/TLN1 axis[J]. J Cancer,2022,13(2):541-553. [16] Guo WW,Feng MM,Li SF,et al.Circular RNA circ_0023404 serves as a miR-636 sponge to promote malignant behaviors in cervical cancer cells through upregulation of CYP2S1[J]. Kaohsiung J Med Sci,2022,38(3):218-229. [17] Zhang CY,Liu P,Huang JM,et al.Circular RNA hsa_circ_0043280 inhibits cervical cancer tumor growth and metastasis via miR-203a-3p/PAQR3 axis[J]. Cell Death Dis,2021,12(10):888-900. [18] Li J,Guo RB,Liu Q,et al.Circular RNA circ-ITCH inhibits the malignant behaviors of cervical cancer by microRNA-93-5p/FOXK2 axis[J]. Reprod Sci,2020,27(3):860-868. [19] Deng T,Liu Y,Yang YL,et al.Regulation of microRNA miR-197-3p/CDC28 protein kinase regulatory subunit 1B(CKS1B)axis by Circular RNA hsa_circ_0000285 promotes glioma progression[J]. Bioengineered,2022,13(3):4757-4772. [20] Zhang ZC,Pu FF,Wang BC,et al.Hsa_circ_0000285 functions as a competitive endogenous RNA to promote osteosarcoma progression by sponging hsa-miRNA-599[J]. Gene Ther,2020,27(5):186-195.