Aurora-A promotes lenvatinib resistance experimentally through hsa-circ-0058046/miR-424-5p/FGFR1 axis in hepatocellular carcinoma.

IF 3.5 3区 医学
Mubalake Abudoureyimu, Ni Sun, Weiwei Chen, Xinrong Lin, Fan Pan, Rui Wang
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引用次数: 0

Abstract

Objective: This study aimed to investigate whether the dysregulation of Aurora-A is involved in lenvatinib resistance in hepatocellular carcinoma.

Methods: Bioinformatics tools and drug sensitivity assays were used to investigate the association between Aurora-A expression level and lenvatinib resistance in hepatocellular carcinoma cell lines. Cell function experiments had performed after treatment with lenvatinib and/or a selective Aurora-A inhibitor (MLN-8237). CircRNA microarray, RIP, RNA pull-down, and dual-luciferace reporter assay were performed to identify the downstream molecular mechanism of Aurora-A dysregulation.

Results: Aurora-A expression was positively correlated with lenvatinib resistance in hepatocellular carcinoma cells. The Aurora-A selective inhibitor MLN-8237, in combination with lenvatinib, synergistically inhibited hepatocellular carcinoma cell proliferation in vitro and vivo, suggesting the Aurora-A might be a potential therapeutic target for lenvatinib resistance. Mechanistically, Aurora-A induced FGFR1 expression through the hsa-circ-0058046/miR-424-5p/FGFR1 axis. Aurora-A promotes lenvatinib resistance through hsa-circ-0058046/miR-424-5p/FGFR1 axis in hepatocellular carcinoma cells. The simultaneous inhibition of FGFR1 by the Aurora-A inhibitor MLN-8237 and lenvatinib overcame lenvatinib resistance in hepatocellular carcinoma cells.

Conclusion: Collectively, our findings indicate that Aurora-A promotes lenvatinib resistance through the hsa-circ-0058046/miR-424-5p/FGFR1 axis in hepatocellular carcinoma (HCC) cells. These results suggest that Aurora-A may serve as a therapeutic target for HCC patients exhibiting lenvatinib resistance. Furthermore, the combination of lenvatinib and MLN-8237 shows potential for clinical trials aimed at overcoming lenvatinib resistance.

Aurora-A通过hsa-circ-0058046/miR-424-5p/FGFR1轴促进肝细胞癌对仑伐替尼的耐药性实验。
目的:本研究旨在探讨肝细胞癌中Aurora-A基因的异常是否与lenvatinib耐药有关。方法:采用生物信息学手段和药敏试验研究肝癌细胞株Aurora-A表达水平与lenvatinib耐药的关系。用lenvatinib和/或选择性Aurora-A抑制剂(MLN-8237)治疗后进行细胞功能实验。通过CircRNA微阵列、RIP、RNA下拉和双荧光报告基因检测来确定Aurora-A失调的下游分子机制。结果:肝癌细胞中Aurora-A的表达与lenvatinib耐药呈正相关。Aurora-A选择性抑制剂MLN-8237与lenvatinib联合在体外和体内可协同抑制肝癌细胞增殖,提示Aurora-A可能是lenvatinib耐药的潜在治疗靶点。在机制上,Aurora-A通过hsa-circ-0058046/miR-424-5p/FGFR1轴诱导FGFR1表达。Aurora-A在肝癌细胞中通过hsa-circ-0058046/miR-424-5p/FGFR1轴促进lenvatinib耐药。Aurora-A抑制剂MLN-8237和lenvatinib同时抑制FGFR1克服了肝癌细胞中lenvatinib的耐药。结论:总的来说,我们的研究结果表明,在肝细胞癌(HCC)细胞中,Aurora-A通过hsa-circ-0058046/miR-424-5p/FGFR1轴促进lenvatinib耐药性。这些结果表明,Aurora-A可能作为lenvatinib耐药HCC患者的治疗靶点。此外,lenvatinib和MLN-8237的联合应用显示出克服lenvatinib耐药的临床试验潜力。
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来源期刊
International Journal of Immunopathology and Pharmacology
International Journal of Immunopathology and Pharmacology Immunology and Microbiology-Immunology
自引率
0.00%
发文量
88
期刊介绍: International Journal of Immunopathology and Pharmacology is an Open Access peer-reviewed journal publishing original papers describing research in the fields of immunology, pathology and pharmacology. The intention is that the journal should reflect both the experimental and clinical aspects of immunology as well as advances in the understanding of the pathology and pharmacology of the immune system.
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