RETRACTED: Alkannin inhibits proliferation, migration and invasion of hepatocellular carcinoma cells via regulation of miR-92a (Retracted article. See vol. 146, 2022)

被引:13
|
作者
Sun, Baozhen [1 ]
Zhang, Jingzhe [2 ]
Liu, Meihan [3 ]
Guan, Lianyue [1 ]
机构
[1] Jilin Univ, Dept Hepatopancreatobiliary Surg, China Japan Union Hosp, 126 Xiantai St, Changchun 130033, Jilin, Peoples R China
[2] Jilin Univ, China Japan Union Hosp, Dept Orthoped, Changchun 130033, Jilin, Peoples R China
[3] Jilin Univ, China Japan Union Hosp, Dept Ultrasound, Changchun 130033, Jilin, Peoples R China
关键词
Hepatocellular carcinoma; Alkannin; miR-92a; PTEN/PI3K/AKT; COLORECTAL-CANCER; SIGNALING PATHWAY; TUMOR-GROWTH; CONTRIBUTES; METASTASIS; DEREGULATION; EXPRESSION; DIAGNOSIS; SHIKONIN; PCR;
D O I
10.1016/j.biopha.2019.108782
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background/aims: Hepatocellular carcinoma (HCC) is a leading cause of cancer-related death worldwide. In our study, we aimed to investigate the effects of alkannin on HCC cells growth, migration and invasion. Methods: Huh7 and Hep3B2.1-7 cells were treated with alkannin. Expression of miR-92a in cell was altered by transfection with miR-92a-mimic (miR-92a-M) or miR-92a-inhibitor (miR-92a-I). Cell viability, proliferation, apoptosis, migration and invasion were detected by Cell Counting Kit-8, BrdU assay, flow cytometry, and transwell assay, respectively. The expression of miR-92a was determined by quantitative real-time PCR. The expression of proteins associated with proliferation, apoptosis and metastasis was measured by Western blot. Results: Alkannin decreased cell viability and proliferation, executed cell apoptosis, and inhibited the migration and invasion of Huh7 and Hep3B2.1-7 cells. Alkannin negatively regulated the expression of miR-92a, and transfection with miR-92a-M impeded alkannin's anti-tumor functions. PTEN and TP53INP1 were found to be target genes of miR-92a. Alkannin inhibited PTEN-dependent PI3K/AKT pathway. Furthermore, the biological effects of miR-92a-I in alkannin treated cells were eliminated by PTEN silencing. Conclusion: Alkannin exerted anti-tumor activities by downregulation of miR-92a. This process might be executed by inactivating PTEN/PI3K/AKT signal pathways through the binding effects of miR-92a on PTEN.
引用
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页数:9
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