橄榄苦苷通过circMBOAT2/miR-106a-5p信号通路调控口腔鳞癌细胞CAL27增殖和凋亡的机制
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Mechanism of olivin regulating the proliferation and apoptosis of oral squamous cell carcinoma cell CAL27 through circMBOAT2/Mir-106a-5P signaling pathway
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    摘要:

    探讨橄榄苦苷对circMBOAT2/miR-106a-5p 信号通路的调控作用及其对口腔鳞癌细胞CAL27增殖和凋亡的影响。方法 应用实时定量聚合酶链反应(RT-qPCR)检测circMBOAT2和miR-106a-5p在口腔鳞癌组织和癌旁组织中的表达水平。将口腔鳞癌细胞CAL27分为橄榄苦苷(0、200、400、800 μg/mL)组、si-NC组、si-circMBOAT2组、橄榄苦苷800μg/mL+pcDNA-circMBOAT2组。采用RT-qPCR检测各组细胞中circMBOAT2和miR-106a-5p的表达水平,检测并验证circMBOAT2与口腔鳞癌的相关性。应用CCK-8法、集落形成实验、流式细胞术测定CAL27细胞的增殖活力、集落形成能力和凋亡率。应用双荧光素酶实验确定 circMBOAT2和miR-106a-5p靶向关系。结果 口腔鳞癌组织中circMBOAT2表达显著高于癌旁组织(P<0.05),miR-106a-5p表达显著低于癌旁组织(P<0.05)。与橄榄苦苷0μg/mL组比较,橄榄苦苷(200、400、800 μg/mL)组CAL27细胞集落形成数、circMBOAT2水平显著降低(P<0.05),抑制率、凋亡率、miR-106a-5p水平显著升高(P<0.05)。与si-NC组比较,si-circMBOAT2组CAL27细胞集落形成数显著降低(P<0.05),抑制率、凋亡率、miR-106a-5p水平显著升高(P<0.05)。circMBOAT2与miR-106a-5p直接特异性结合。与橄榄苦苷800 μg/mL组比较,橄榄苦苷800μg/mL+pcDNA-circMBOAT2组CAL27细胞集落形成数显著升高(P<0.05),抑制率、凋亡率显著降低(P<0.05)。结论 橄榄苦苷通过下调circMBOAT2/miR-106a-5p通路可抑制口腔鳞癌细胞CAL27增殖,诱导细胞凋亡。

    Abstract:

    To explore the regulation of oleuropein on the circMBOAT2/miR 106a 5p signaling pathway and further to explore its effect on the proliferation and apoptosis of oral squamous cell carcinoma cell CAL27. Methods Realtime quantitative polymerase chain reaction (RT-qPCR) was used to detect the expression of circMBOAT2 and miR-106a-5p in oral squamous cell carcinoma and adjacent tissues. Oral squamous cell carcinoma CAL27 was divided into different concentrations (0, 200, 400, 800 μg/mL) of olivopicroside group, si-NC group, si-circMBOAT2 group and 800 μg/mL+ pcDNA-circMBOAT2 group. The expression of circMBOAT2/miR-106a-5p in each group was detected by RT-qPCR, detection and validation of the correlation between circMBOAT2 and oral squamous cell carcinoma. Proliferation activity, colony forming ability and apoptosis rate of CAL27 cells were measured by CCK- 8 method, colony formation test and flow cytometry. Double luciferase assay was used to determine the targeting relationship between circMBOAT2 and miR-106a-5p. Results circMBOAT2 expression in oral squamous cell carcinoma tissue was significantly higher than that in adjacent tissues (P<0.05), while miR-106a-5p expression was significantly lower than that in adjacent tissues (P<0.05).Compared with the oleuropein 0 μg/mL group, the colony formation number and circMBOAT2 levels of CAL27 cells in the oleuropein (200, 400, 800 μg/mL) group were notably reduced (P<0.05), and the inhibition rate, apoptosis rate and miR-106a-5p levels were notably increased (P<0.05). Compared with the si-NC group, the colony formation number of CAL27 cell in the si-circMBOAT2 group was notably reduced (P<0.05), and the inhibition rate, apoptosis rate and miR-106a-5p levels were notably increased (P<0.05). circMBOAT2 directly and specifically bound to miR 106a 5p. Compared with the oleuropein 800 μg/mL group, the colony formation number of CAL27 cells in the oleuropein 800 μg/mL+pcDNA circMBOAT2 group was notably increased (P<0.05), and the inhibition rate and apoptosis rate were significantly reduced (P<0.05).Conclusion Oleuropein inhibits oral squamous cell carcinoma cells CAL27 proliferation and induce cell apoptosis by down-regulating the circMBOAT2/miR-106a-5p pathway.

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  • 在线发布日期: 2022-11-21
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