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微小 RNA-384 在人前列腺癌细胞中低表达,并通过作用于 HOXB7 发挥抗肿瘤功能。

MicroRNA-384 is lowly expressed in human prostate cancer cells and has anti-tumor functions by acting on HOXB7.

机构信息

Department of Andrology, Shenzhen Traditional Chinese Medicine Hospital, Shenzhen, 518033, Guangdong, China.

Department of Andrology, Shenzhen Baoan Traditional Chinese Medicine Hospital, Shenzhen, 518133, Guangdong, China.

出版信息

Biomed Pharmacother. 2019 Jun;114:108822. doi: 10.1016/j.biopha.2019.108822. Epub 2019 Apr 2.

DOI:10.1016/j.biopha.2019.108822
PMID:30951946
Abstract

OBJECTIVES

In this work, we evaluated the expression of microRNA-384 (miR-384) in human prostate cancer (CAP) cells and its regulatory role on CAP in vitro and in vivo functions.

METHODS

In CAP cell lines, miR-384 expression was evaluated by qRT-PCR. In LNCaP and VCaP cells, lentiviral infection was done to overexpress miR-384. The regulatory effects of miR-384 overexpression on CAP in vitro proliferation and migration, and in vivo tumorigenesis, were evaluated, respectively. The targeting of miR-384 on Homeobox b7 gene (HOXB7), was evaluated by dual-luciferase reporter assay and qRT-PCR. In addition, HOXB7 was upregulated in miR-384-overexpressed CAP cells to evaluate the correlated role of HOXB7 in miR-384-mediated CAP proliferation and migration in vitro.

RESULTS

MiR-384 was lowly expressed in CAP cell lines. Lentiviral infection induced miR-384 overexpression inhibited CAP in vitro proliferation and migration, and in vivo tumorigenesis. HOXB7 was directly targeted by miR-384 in CAP cells. In miR-384-overexpressed CAP cells, HOXB7 upregulation reversed the effect of miR-384 by promoting CAP in vitro proliferation and migration.

CONCLUSION

MiR-384 was downregulated in CAP cells. MiR-384 overexpression suppressed CAP in vitro and in vivo development, possibly via acting through its downstream target gene of HOXB7.

摘要

目的

在这项工作中,我们评估了 microRNA-384(miR-384)在人前列腺癌(CAP)细胞中的表达及其对 CAP 的体外和体内功能的调节作用。

方法

在 CAP 细胞系中,通过 qRT-PCR 评估 miR-384 的表达。在 LNCaP 和 VCaP 细胞中,通过慢病毒感染过表达 miR-384。分别评估 miR-384 过表达对 CAP 体外增殖和迁移以及体内肿瘤发生的调节作用。通过双荧光素酶报告基因检测和 qRT-PCR 评估 miR-384 对同源盒 B7 基因(HOXB7)的靶向作用。此外,在 miR-384 过表达的 CAP 细胞中上调 HOXB7,以评估 HOXB7 在 miR-384 介导的 CAP 体外增殖和迁移中的相关作用。

结果

miR-384 在 CAP 细胞系中低表达。慢病毒感染诱导 miR-384 过表达抑制 CAP 体外增殖和迁移以及体内肿瘤发生。HOXB7 是 CAP 细胞中 miR-384 的直接靶标。在 miR-384 过表达的 CAP 细胞中,HOXB7 的上调通过促进 CAP 体外增殖和迁移来逆转 miR-384 的作用。

结论

miR-384 在 CAP 细胞中下调。miR-384 过表达抑制 CAP 的体外和体内发育,可能是通过其下游靶基因 HOXB7 发挥作用。

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