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抑制 microRNA-301b 可抑制宫颈癌中的细胞生长并靶向 RNF38。

Inhibiting microRNA-301b suppresses cell growth and targets RNF38 in cervical carcinoma.

机构信息

Department of Obstetrics, Binzhou Central Hospital, Binzhou, Shandong, China.

Department of Emergency, Binzhou Central Hospital, Binzhou, Shandong, China.

出版信息

Kaohsiung J Med Sci. 2020 Nov;36(11):878-884. doi: 10.1002/kjm2.12273. Epub 2020 Jul 9.

Abstract

It has been reported microRNA-301b (miR-301b) was involved in the tumorigenesis of some cancers, but it has not been investigated in cervical carcinoma yet. In this study, miR-301b was found significantly upregulated in cervical carcinoma, and patients with high miR-301b expression had a shorter overall survival. When miR-301b was knocked down in cervical carcinoma cells, the cell growth could be significantly abolished. Our further studies showed miR-301b targeted RNF38, and inhibited its expression in cervical carcinoma cells. Moreover, RNF38 was found downregulated in cervical carcinoma, and miR-301b expression in cervical tissues was found negatively correlated with RNF38 expression. In addition, overexpression of RNF38 significantly inhibited cervical carcinoma cell growth, but overexpression of miR-301b suppressed RNF38-induced cell growth inhibition in cervical carcinoma. Collectively, this study suggested miR-301b could be a novel target for cervical carcinoma treatment.

摘要

已有报道称 microRNA-301b(miR-301b)参与了一些癌症的肿瘤发生,但尚未在宫颈癌中进行研究。在本研究中,发现 miR-301b 在宫颈癌中显著上调,miR-301b 高表达的患者总生存期较短。当在宫颈癌细胞中敲低 miR-301b 时,细胞生长可显著被抑制。我们的进一步研究表明 miR-301b 靶向 RNF38,并抑制其在宫颈癌细胞中的表达。此外,在宫颈癌中发现 RNF38 下调,并且在宫颈癌组织中发现 miR-301b 的表达与 RNF38 的表达呈负相关。此外,过表达 RNF38 显著抑制宫颈癌细胞生长,但过表达 miR-301b 抑制了 RNF38 诱导的宫颈癌细胞生长抑制。总之,本研究表明 miR-301b 可能成为宫颈癌治疗的新靶点。

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