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长链非编码RNA NEAT1/微小RNA-766-5p/E2F3调控轴促进前列腺癌进展。

The lncRNA NEAT1/miRNA-766-5p/E2F3 Regulatory Axis Promotes Prostate Cancer Progression.

作者信息

Zhao Wenhui, Zhu Xinshu, Jin Qiu, Lin Bo, Ji Runyuan

机构信息

Department of Pathology, Huai'an Key Laboratory of Gastric Cancer, Jiangsu College of Nursing, Huai'an, Jiangsu 223001, China.

出版信息

J Oncol. 2022 Feb 21;2022:1866972. doi: 10.1155/2022/1866972. eCollection 2022.

Abstract

BACKGROUND

Prostate cancer (PCa) is one of the most common malignancies in men. Increasing evidence has demonstrated that dysregulation of long noncoding RNAs (lncRNAs) is closely related to carcinogenesis and cancer progression. lncRNA NEAT1 has recently been identified as a carcinogenic regulator of multiple cancers; however, the role of NEAT1 on PCa is still poorly understood.

METHODS

Kaplan-Meier was conducted to determine the overall survival rate in PCa patients with aberrant NEAT1 levels. qRT-PCR analysis was performed to detect expressions of NEAT1 and miR-766-5p in tissues and cells. In addition, CCK-8, colony formation, flow cytometry analysis, wound healing, and transwell assay were conducted to determine cell proliferation, cell arrest, apoptosis, migration, and invasion. The western blot assay was utilized to determine E2F3 and cell growth-related proteins. The relationship between NEAT1 and miR-766-5p or miR-766-5p and E2F3 was verified by correlation analysis and dual-luciferase reporter assay.

RESULTS

Here, we find that NEAT1 is overexpressed in PCa tissues and cell lines. Besides, silencing of NEAT1 inhibits cell proliferation, invasion, and migration and promotes cell apoptosis and cell cycle arrest. Further mechanistic studies find that NEAT1 sponges miR-766-5p, and miRNA-766-5p is negatively correlated with the expression of NEAT1. In addition, the functional experiment shows that upregulation of miRNA-766-5p inhibits PCa proliferation, migration, and invasion. Furthermore, E2F transcription factor 3 (E2F3) is testified to be the downstream target gene of miRNA-766-5p. Finally, the rescue experiment revealed that miRNA-766-5p inhibition largely restores NEAT1 downregulation-mediated function on PCa progression, while E2F3 knockdown partly removes the effects of miRNA-766-5p inhibitor.

CONCLUSIONS

In conclusion, NEAT1 facilitates PCa progression by targeting the miRNA-766-5p/E2F3 axis.

摘要

背景

前列腺癌(PCa)是男性最常见的恶性肿瘤之一。越来越多的证据表明,长链非编码RNA(lncRNA)的失调与癌症发生和进展密切相关。lncRNA NEAT1最近被确定为多种癌症的致癌调节因子;然而,NEAT1在PCa中的作用仍知之甚少。

方法

采用Kaplan-Meier法确定NEAT1水平异常的PCa患者的总生存率。进行qRT-PCR分析以检测组织和细胞中NEAT1和miR-766-5p的表达。此外,进行CCK-8、集落形成、流式细胞术分析、伤口愈合和transwell试验以确定细胞增殖、细胞停滞、凋亡、迁移和侵袭。利用蛋白质免疫印迹法测定E2F3和细胞生长相关蛋白。通过相关性分析和双荧光素酶报告基因试验验证NEAT1与miR-766-5p或miR-766-5p与E2F3之间的关系。

结果

在此,我们发现NEAT1在PCa组织和细胞系中过表达。此外,沉默NEAT1可抑制细胞增殖、侵袭和迁移,并促进细胞凋亡和细胞周期停滞。进一步的机制研究发现,NEAT1可吸附miR-766-5p,且miRNA-766-5p与NEAT1的表达呈负相关。此外,功能实验表明,上调miRNA-766-5p可抑制PCa的增殖、迁移和侵袭。此外,E2F转录因子3(E2F3)被证实是miRNA-766-5p的下游靶基因。最后,挽救实验表明,抑制miRNA-766-5p可在很大程度上恢复NEAT1下调介导的对PCa进展的作用,而敲低E2F3可部分消除miRNA-766-5p抑制剂的作用。

结论

总之,NEAT1通过靶向miRNA-766-5p/E2F3轴促进PCa进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3b4/8885187/af09f8fb1336/JO2022-1866972.006.jpg

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