首页|circ_0008043通过miR-198/SLC2A1轴促进肝癌糖酵解及肝癌发展

circ_0008043通过miR-198/SLC2A1轴促进肝癌糖酵解及肝癌发展

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目的 探究circ_0008043 调控肝癌细胞糖酵解的机制.方法 采用qPCR检测临床样本和肝癌细胞系中circ_0008043、miR-198 和SLC2A1 的表达,并用双荧光素酶报告实验验证circ_0008043 与miR-198 及miR-198 与SLC2A1 的靶向结合;通过向肝癌细胞系转染sh-circ_0008043/sh-NC、miR-198 inhibitor/miR-198 inhibitor-NC、miR-198 mimic/mimic NC或pcDNA3.1-SLC2A1/pcDNA3.1-NC检测circ_0008043、miR-198 和SLC2A1 对肝癌细胞糖酵解的影响;通过裸鼠移植瘤模型验证circ_0008043 对肝癌肿瘤生长的影响.结果 circ_0008043 在肝癌组织与细胞系中均高表达(P<0.01),沉默circ_0008043 可抑制肝癌细胞糖酵解;miR-198 在肝癌组织与细胞系中表达降低(P<0.001)且与circ_0008043 表达呈负相关(r=-0.550,P<0.001),沉默circ_0008043 对糖酵解造成的抑制可通过抑制miR-198 的表达被部分恢复;SLC2A1 在肝癌组织与肝癌细胞系中表达水平高(P<0.001),过表达SLC2A1 可逆转由过表达miR-198 对肝癌细胞糖酵解产生的抑制作用.裸鼠移植瘤实验表明,沉默circ_0008043 可抑制肝癌肿瘤的生长(P<0.001).结论 circ_0008043 通过miR-198/SLC2A1 轴促进肝癌细胞糖酵解及肝癌的生长.
circ_0008043 promotes glycolysis of hepatocellular carcinoma and the development of hepatocellular carcinoma through miR-198/SLC2A1 axis
Objective The aim of this study was to investigate the mechanism of circ_0008043 regulating glycolysis of hepa-tocellular carcinoma(HCC)cells.Methods The expression of circ_0008043,miR-198 and SLC2A1 in clinical samples and HCC cell lines was detected by qPCR,and the targeted binding of circ_0008043 to miR-198 and miR-198 to SLC2A1 was verified by dual luciferase reporting assay.HCC cells were transfected with sh-circ_0008043/sh-NC,miR-198 inhibitor/miR-198 inhibitor-NC,miR-198 mimic/mimic NC,or pcDNA3.1-SLC2A1/pcDNA3.1-NC to detected the effects of circ_0008043,miR-198 and SLC2A1 on the glycolysis of HCC cells.The effect of circ_0008043 on tumor growth in HCC was verified by HCC cell xenografts through a nude mouse model.Results circ_0008043 was highly expressed in both HCC tissues and cell lines(P<0.01).Silencing circ_0008043 could inhibit the glycolysis of HCC cells.The expression of miR-198 was decreased in HCC tissues and cell lines(P<0.001)and neg-atively correlated with the expression of circ_0008043(r=-0.550,P<0.001).The inhibition of glycolysis caused by silencing circ_0008043 was partially restored by inhibiting miR-198 expression.SLC2A1 was highly expressed in HCC tissues and cell lines(P<0.001),and overexpression of SLC2A1 reversed the inhibitory effect of miR-198 on glycolysis in HCC cells.The nude mouse experi-ment showed that silencing circ_0008043 could inhibit the growth of HCC cell xenografts(P<0.001).Conclusion circ_0008043 promotes HCC cell glycolysis and growth through the miR-198/SLC2A1 axis.

Hepatocellular carcinomaGlycolysiscirc_0008043miR-198SLC2A1

张康军、方泰石、岑福兰、闫旭、陈琦军、马楠

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深圳市第三人民医院肝脏外科(肝移植)(南方科技大学第二附属医院)(深圳 518000)

肝癌 糖酵解 circ_0008043 miR-198 SLC2A1

2024

实用肿瘤学杂志
黑龙江省,辽宁省,吉林省肿瘤防治办公室

实用肿瘤学杂志

CSTPCD
影响因子:0.528
ISSN:1002-3070
年,卷(期):2024.38(6)