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微小 RNA miR-330-3p 通过靶向 RIPK4 抑制卵巢癌的进展。

MicroRNA miR-330-3p suppresses the progression of ovarian cancer by targeting RIPK4.

机构信息

Department of Oncology, Jiangxi Maternal and Child Health Hospital , Nanchang, Jiangxi, China.

Department of Pathology, Jiangxi Maternal and Child Health Hospital , Nanchang, Jiangxi, China.

出版信息

Bioengineered. 2021 Dec;12(1):440-449. doi: 10.1080/21655979.2021.1871817.

DOI:10.1080/21655979.2021.1871817
PMID:33487072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8291835/
Abstract

Previous studies reported that miR-330-3p was involved in the progression of several cancers, but the potential roles of miR-330-3p in ovarian cancer (OC) were unclear. In the current study, we aimed to explore the expression pattern and functions of miR-330-3p in OC. The expression level of miR-330-3p in OC tissues and cell lines was detected using RT-qPCR. The proliferation, migration and invasion of OC cells were detected using CCK-8 assay and transwell assay, respectively. Bioinformatics analysis and luciferase reporter assay were used to analyze the targeted binding site of miR-330-3p and RIPK4. The results showed that miR-330-3p was significantly downregulated in OC tissues and cell lines. Overexpression of miR-330-3p inhibited the proliferation, migration and invasion of OC cells. Mechanistically, a dual-luciferase reported assay showed that RIPK4 is a target gene of miR-330-3p. Furthermore, rescue experiments revealed that miR-330-3p suppressed the proliferation, migration and invasion of OC cells by targeting RIPK4. In summary, our findings indicated that miR-330-3p suppressed the progression of OC by targeting RIPK4. Our results indicated that miR-330-3p/RIPK4 axis might act as a novel therapeutic target for OC treatment.

摘要

先前的研究报告表明,miR-330-3p 参与了几种癌症的进展,但 miR-330-3p 在卵巢癌(OC)中的潜在作用尚不清楚。在本研究中,我们旨在探讨 miR-330-3p 在 OC 中的表达模式和功能。使用 RT-qPCR 检测 OC 组织和细胞系中 miR-330-3p 的表达水平。使用 CCK-8 测定法和 Transwell 测定法分别检测 OC 细胞的增殖、迁移和侵袭。生物信息学分析和荧光素酶报告基因测定用于分析 miR-330-3p 和 RIPK4 的靶向结合位点。结果表明,miR-330-3p 在 OC 组织和细胞系中显著下调。miR-330-3p 的过表达抑制了 OC 细胞的增殖、迁移和侵袭。机制上,双荧光素酶报告基因测定显示 RIPK4 是 miR-330-3p 的靶基因。此外,挽救实验表明,miR-330-3p 通过靶向 RIPK4 抑制 OC 细胞的增殖、迁移和侵袭。总之,我们的研究结果表明,miR-330-3p 通过靶向 RIPK4 抑制 OC 的进展。我们的结果表明,miR-330-3p/RIPK4 轴可能成为 OC 治疗的新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/8291835/f6514389a744/KBIE_A_1871817_F0005_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/8291835/b3908c28f44d/KBIE_A_1871817_UF0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/8291835/ffe06d305cb7/KBIE_A_1871817_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/8291835/c90b3ec21dee/KBIE_A_1871817_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/8291835/7bfd73d223c0/KBIE_A_1871817_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/8291835/78013b911ce8/KBIE_A_1871817_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/8291835/f6514389a744/KBIE_A_1871817_F0005_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/8291835/b3908c28f44d/KBIE_A_1871817_UF0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/8291835/ffe06d305cb7/KBIE_A_1871817_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/8291835/c90b3ec21dee/KBIE_A_1871817_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/8291835/7bfd73d223c0/KBIE_A_1871817_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/8291835/78013b911ce8/KBIE_A_1871817_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55e0/8291835/f6514389a744/KBIE_A_1871817_F0005_B.jpg

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