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微小RNA-186抑制人皮肤恶性黑色素瘤细胞的增殖和侵袭。

MiR-186 inhibits cell proliferation and invasion in human cutaneous malignant melanoma.

作者信息

Su Bei-Bei, Zhou Shu-Wei, Gan Cai-Bin, Zhang Xiao-Ning

机构信息

Department of Dermatology, Xinxiang Central Hospital, Xinxiang, Henan, China.

Department of Head and Neck, and Breast Surgery, Xinxiang Central Hospital, Xinxiang, Henan, China.

出版信息

J Cancer Res Ther. 2018;14(Supplement):S60-S64. doi: 10.4103/0973-1482.157340.

Abstract

AIMS

MicroRNA-186 (miR-186) has been shown to be involved in various types of cancer. The purpose of this study was to investigate the expression level and functional role of miR-186 in human cutaneous malignant melanoma cells.

SUBJECTS AND METHODS

Expression of miR-186 was analyzed in human cutaneous malignant melanoma (CMM) cell lines SK-MEL-1, G-361, A375 and A875, and human normal epidermal melanocytes cell line HEMn-LP by quantitative reverse transcription polymerase chain reaction (qRT-PCR). Additionally, the functional role of miR-186 on melanoma cells was investigated by transfection of miR-186 mimic followed by analyses of cell proliferation, apoptosis, and metastasis.

RESULTS

We found that the expression levels of miR-186 were decreased in CMM cell lines compared with normal epidermal melanocytes cell line. Moreover, overexpression of miR-186 inhibited cells proliferation through abrogating the G-S transition, and reduced cells migration and invasion.

CONCLUSIONS

Our findings suggested that miR-186 exhibit an inhibitory effect on CMM cell proliferation, migration, and invasion; thus, may serve as a potential therapeutic target for human CMM intervention.

摘要

目的

微小RNA-186(miR-186)已被证明参与多种类型的癌症。本研究的目的是调查miR-186在人皮肤恶性黑色素瘤细胞中的表达水平和功能作用。

对象与方法

通过定量逆转录聚合酶链反应(qRT-PCR)分析miR-186在人皮肤恶性黑色素瘤(CMM)细胞系SK-MEL-1、G-361、A375和A875以及人正常表皮黑素细胞系HEMn-LP中的表达。此外,通过转染miR-186模拟物,然后分析细胞增殖、凋亡和转移,研究miR-186对黑色素瘤细胞的功能作用。

结果

我们发现,与正常表皮黑素细胞系相比,CMM细胞系中miR-186的表达水平降低。此外,miR-186的过表达通过消除G-S期转换抑制细胞增殖,并减少细胞迁移和侵袭。

结论

我们的研究结果表明,miR-186对CMM细胞的增殖、迁移和侵袭具有抑制作用;因此,可能作为人类CMM干预的潜在治疗靶点。

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