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微小RNA-330-5p调控酪氨酸酶和蛋白质二硫键异构酶A3的表达,并抑制皮肤恶性黑色素瘤细胞的增殖和侵袭。

MiR-330-5p regulates tyrosinase and PDIA3 expression and suppresses cell proliferation and invasion in 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, People's Republic of China.

Department of Head, Neck, and Breast Surgery, Xinxiang Central Hospital, Xinxiang, Henan, People's Republic of China.

出版信息

J Surg Res. 2016 Jun 15;203(2):434-40. doi: 10.1016/j.jss.2016.03.021. Epub 2016 Mar 19.

Abstract

BACKGROUND

Increasing evidence has suggested that miR-330-5p can function as a tumor suppressor in different types of cancers. However, the effects and underlying mechanisms of miR-330-5p in the development of cutaneous malignant melanoma (CMM) remain largely unknown. The aim of the present study was to investigate the role of miR-330-5p in CMM and to determine the molecular mechanisms underlying its action.

MATERIALS AND METHODS

The expression level of miR-330-5p was detected in 26 cases of primary CMM tissues and cell lines by real-time quantitative polymerase chain reaction. We also assessed whether overexpression of miR-330-5p influences in vitro cell proliferation, invasion, and migration. Western blotting analysis was used to detect the influence of miR-330-5p on the targets, and Pearson analysis was used to calculate the correlation between the expression of targets gene and miR-330-5p in CMM tissues.

RESULTS

Our study showed that miR-330-5p was downregulated in CMM tissues (P = 0.010) and cell lines (P < 0.05), and patients with high mitotic activity showed lower miR-330-5p expression levels (P = 0.002). Enforced expression of miR-330-5p inhibits malignant CMM cells proliferation and migration and led to downregulation of the TYR and PDIA3 protein. Moreover, the expression level of miR-330-5p in CMM tissues showed inverse relationship with the expression level of TYR and PDIA3 protein.

CONCLUSIONS

In conclusion, our findings suggested that miR-330-5p represents a potential tumor-suppressive miRNA and plays an important role in CMM progression by suppressing TYR and PDIA3 expression.

摘要

背景

越来越多的证据表明,miR-330-5p在不同类型的癌症中可作为一种肿瘤抑制因子发挥作用。然而,miR-330-5p在皮肤恶性黑色素瘤(CMM)发生发展中的作用及其潜在机制仍不清楚。本研究旨在探讨miR-330-5p在CMM中的作用,并确定其作用的分子机制。

材料与方法

采用实时定量聚合酶链反应检测26例原发性CMM组织和细胞系中miR-330-5p的表达水平。我们还评估了miR-330-5p的过表达是否会影响体外细胞的增殖、侵袭和迁移。采用蛋白质免疫印迹分析检测miR-330-5p对靶标的影响,并用Pearson分析计算靶标基因表达与CMM组织中miR-330-5p表达之间的相关性。

结果

我们的研究表明,miR-330-5p在CMM组织(P = 0.010)和细胞系(P < 0.05)中表达下调,有丝分裂活性高的患者miR-330-5p表达水平较低(P = 0.002)。miR-330-5p的过表达抑制了恶性CMM细胞的增殖和迁移,并导致TYR和PDIA3蛋白表达下调。此外,CMM组织中miR-330-5p的表达水平与TYR和PDIA3蛋白的表达水平呈负相关。

结论

总之,我们的研究结果表明,miR-330-5p是一种潜在的肿瘤抑制性微小RNA,通过抑制TYR和PDIA3的表达在CMM进展中发挥重要作用。

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