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HGF/c-Met 通过上调 circ-CCDC66 促进肾癌细胞癌干细胞富集。

HGF/c-Met Promote Renal Carcinoma Cancer Stem Cells Enrichment Through Upregulation of Cir-CCDC66.

机构信息

Department of Nephrology, The First People's Hospital of Jingmen, Jingmen, Hubei, China.

Department of Urology Surgery, The First People's Hospital of Jingmen, Jingmen, Hubei, China.

出版信息

Technol Cancer Res Treat. 2020 Jan-Dec;19:1533033819901114. doi: 10.1177/1533033819901114.

Abstract

Increasing studies have suggested that circular RNAs play an important function in the process of numerous cancers. We aimed to investigate the possible role of cir-CCDC66 in renal carcinoma cancer. As cancer stem cells are responsible for the renal carcinoma cancer tumor growth and resistance to conventional therapy, we focus on the cir-CCDC66 influence on renal carcinoma cancer stem cells. In this study, we performed experiments in human renal tubular epithelial cell HK2 cells and several renal carcinoma cancer cancer cell lines. The results showed that cir-CCDC66 was upregulated not only in renal carcinoma cancer cancer cell lines but also in cancer stem cell spheres. What's more, the results showed that cir-CCDC66 enhanced the cancer stem cell enrichment. Further mechanistic studies showed that hepatocyte growth factor/c-Met pathway was activated in cancer stem cell enrichment and responsible for the cir-CCDC66 upregulation. Inhibition of hepatocyte growth factor/c-Met could block cir-CCDC66-induced cancer stem cell enrichment. In conclusion, our research revealed a novel mechanism between hepatocyte growth factor/c-Met/cir-CCDC66 and cancer stem cell enrichment. We verified that cir-CCDC66 could be a promising biomarker and therapy target for renal carcinoma cancer treatment.

摘要

越来越多的研究表明,环状 RNA 在多种癌症的发生过程中发挥着重要作用。我们旨在研究 cir-CCDC66 在肾细胞癌中的可能作用。由于癌症干细胞负责肾细胞癌肿瘤的生长和对常规治疗的耐药性,我们专注于 cir-CCDC66 对肾癌细胞干细胞的影响。在这项研究中,我们在人肾小管上皮细胞 HK2 细胞和几种肾癌细胞系中进行了实验。结果表明,cir-CCDC66 不仅在肾癌细胞系中上调,而且在癌症干细胞球中也上调。更重要的是,结果表明 cir-CCDC66 增强了癌症干细胞的富集。进一步的机制研究表明,在癌症干细胞富集中激活了肝细胞生长因子/c-Met 通路,并且该通路负责 cir-CCDC66 的上调。抑制肝细胞生长因子/c-Met 可以阻断 cir-CCDC66 诱导的癌症干细胞富集。总之,我们的研究揭示了肝细胞生长因子/c-Met/cir-CCDC66 与癌症干细胞富集之间的新机制。我们验证了 cir-CCDC66 可以作为肾细胞癌治疗有前途的生物标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91b4/6990613/944b7ce08560/10.1177_1533033819901114-fig1.jpg

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