首页|CircFNDC3B 调节 miR-107/HMGA1 轴对胃癌细胞恶性生物学行为的影响

CircFNDC3B 调节 miR-107/HMGA1 轴对胃癌细胞恶性生物学行为的影响

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目的 探讨环状RNA FNDC3B(CircFNDC3B)调节微小RNA-107/高迁移率家族蛋白A1(miR-107/HMGA1)轴对胃癌(GC)细胞恶性生物学行为的影响.方法 体外培养正常胃上皮细胞GES-1和人胃癌细胞系 AGS、HCG27、MKN28、BGC-823,RT-qPCR 检测 CircFNDC3B、miR-107 和 HMGA1 表达,筛选出最佳细胞系.双荧光素酶报告基因实验验证miR-107与CircFNDC3B、HMGA 1的靶向关系;选择BGC-823细胞进行转染,将细胞分为 si-NC 组、si-CircFNDC3B 组、si-CircFNDC3B+NC inhibitor、si-CircFNDC3B+miR-107 inhibi-tor 组、miR-NC 组、miR-107 mimics 组、miR-107 mimics+pcDNA、miR-107 mimics+HMGA1 组,MTT 法检测细胞增殖;Transwell检测细胞迁移和侵袭能力;流式细胞技术检测细胞凋亡;Western blot检测Ki67、Cyclin D1、Bcl-2、cleaved caspase3、E-cadherin、N-cadherin蛋白表达.结果 在胃癌细胞系中 CircFNDC3B、HMGA1 表达显著增加,miR-107表达显著下降(P<0.05);双荧光素酶报告基因实验结果显示,miR-107与CircFNDC3B、HMGA1具有靶向关系;沉默CircFNDC3B表达或过表达miR-107可显著抑制细胞增殖、迁移、侵袭和EMT,促进细胞凋亡(P<0.05);抑制miR-107表达或过表达HMGA 1可逆转沉默CircFNDC3B或过表达miR-107对BGC-823细胞增殖、迁移、侵袭和EMT的抑制作用(P<0.05).结论 CircFNDC3B在胃癌细胞中高表达,沉默CircFNDC3B通过调节miR-107/HMGA1轴抑制胃癌细胞恶性生物学行为.
Effect of CircFNDC3B on the malignant biological behavior of gastric cancer cells by regulating the miR-107/HMGA1 axis
Objective To investigate the impact of circular RNA FNDC3B(CircFNDC3B)on the malig-nant biological behaviors of gastric cancer(GC)cells by regulating the micro RNA-107/high mobility group protein A1(miR-107/HMGA1)axis.Methods Normal gastric epithelial cells GES-1 and human gastric cancer cell lines AGS,HCG27,MKN28,BGC-823 were cultured in vitro,RT-qPCR was applied to detect the expression of CircF-NDC3B,miR-107,and HMGA1,and to screen the optimal cell line.Double Luciferase reporter gene experiment was applied to verify the targeting relationship between miR-107 and CircFNDC3B,HMGA1;BGC-823 cells were selected for transfection and grouped into si-NC group,si-CircFNDC3B group,si-CircFNDC3B+NC inhibitor,si-Cir-cFNDC3B+miR-107 inhibitor group,miR-NC group,miR-107 mics group,miR-107 mics+pcDNA,and miR-107 mics+HMGA1 group,MTT method was applied to detect cell proliferation;Transwell was applied to detect cell mi-gration and invasion;flow cytometry was applied to detect cell apoptosis;Western blot was applied to detect the ex-pression of Ki67,Cyclin D1,Bcl-2,cleaved caspase3,E-cadherin,and N-cadherin proteins.Results In GC cell lines,the expression of CircFNDC3B and HMGA1 obviously increased,while the expression of miR-107 obviously decreased(P<0.05);the results of double luciferase reporter gene experiment showed that miR-107 had a targeting relationship with CircFNDC3B and HMGA1;silencing the expression of CircFNDC3B or overexpressing miR-107 was able to obviously inhibit cell proliferation,migration,invasion,and EMT,and promote cell apoptosis(P<0.05);inhibiting the expression of miR-107 or overexpressing HMGA1 was able to reverse the inhibitory effects of si-lencing CircFNDC3B or overexpressing miR-107 on the proliferation,migration,invasion,and EMT of BGC-823 cells(P<0.05).Conclusion CircFNDC3B is highly expressed in GC cells,and silencing CircFNDC3B inhibits the malignant biological behavior of gastric cancer cells by regulating the miR-107/HMGA1 axis.

Gastric cancer cellsCyclic RNA FNDC3BMicro RNA-107/high mobility group protein A1Malignant biological behavior

李雪龙、李志仁、杨妮

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首都医科大学附属北京朝阳医院消化科,北京 100020

胃癌细胞 环状RNA FNDC3B 微小RNA-107/高迁移率家族蛋白A1 恶性生物学行为

2024

解剖学研究
广东省解剖学会 中国解剖学会

解剖学研究

CSTPCD
影响因子:0.327
ISSN:1671-0770
年,卷(期):2024.46(3)
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