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长链非编码 RNA PVT1/miR186/KLF5 轴对胆管癌发生发展的影响。

Effect of lncRNA PVT1/miR186/KLF5 Axis on the Occurrence and Progression of Cholangiocarcinoma.

机构信息

General Surgery Department, Zhongshan Hospital, Sun Yat-Sen University, Zhongshan, China.

Organ Transplant Center, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.

出版信息

Biomed Res Int. 2021 Jul 10;2021:8893652. doi: 10.1155/2021/8893652. eCollection 2021.

DOI:10.1155/2021/8893652
PMID:34337058
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8286192/
Abstract

This study primarily focused on the effect of the long noncoding RNA (lncRNA) PVT1/miR186/KLF5 axis on the occurrence and progression of cholangiocarcinoma (CCA). miR186 was found both in the lncRNA PVT1 targeting miRNAs and KLF5 targeting miRNAs using bioinformatic analysis. The expression of lncRNA PVT1 and KLF5 in the TFK-1, QBC939, and HuCCT1 cell lines and normal biliary epithelial HIBEpiC cells was detected by RT-qPCR. The significance of lncRNA PVT1 and KLF5 on cell proliferation was analyzed using the MTT assay and clone formation assay in lncRNA PVT1 and KLF5 silencing HuCCT1 cell lines and lncRNA PVT1and KLF5 overexpressing TFK-1 and QBC939 cell lines, respectively. The potential role of lncRNA PVT1 and KLF5 in cell migration was detected using the transwell invasion assay in CCA cell lines and tumor formation assay. Additionally, lncRNA PVT1 and KLF5 were proved to be highly expressed in CCA tissues and cell lines. Silencing and overexpressing of lncRNA PVT1 or KLF5 markedly inhibited or increased the cell proliferation and cell invasion in CCA cell lines, respectively. Silencing and overexpressing of lncRNA PVT1 significantly inhibited and increased the expression of KLF5 in CCA cell lines, respectively. Silencing of lncRNA PVT1 increased the expression of miR186, and silencing of miR186 increased the expression of KLF5 in CCA cell lines. Cotransfection of lncRNA PVT1 and miR186 increased the expression of KLF5 compared with controls. Overall, these results demonstrated that the lncRNA PVT1/miR186/KLF5 axis might exert a key role in the occurrence and progression of CCA, and this axis might provide a new target for treating CCA.

摘要

本研究主要关注长链非编码 RNA(lncRNA)PVT1/miR186/KLF5 轴对胆管癌(CCA)发生和进展的影响。通过生物信息学分析,在 lncRNA PVT1 靶向 miRNA 和 KLF5 靶向 miRNA 中均发现了 miR186。通过 RT-qPCR 检测 TFK-1、QBC939 和 HuCCT1 细胞系和正常胆管上皮 HIBEpiC 细胞中 lncRNA PVT1 和 KLF5 的表达。在 lncRNA PVT1 沉默 HuCCT1 细胞系和 lncRNA PVT1 和 KLF5 过表达 TFK-1 和 QBC939 细胞系中,通过 MTT 测定和克隆形成测定分析 lncRNA PVT1 和 KLF5 对细胞增殖的意义,分别。通过 CCA 细胞系和肿瘤形成测定中转染小室侵袭测定检测 lncRNA PVT1 和 KLF5 在细胞迁移中的潜在作用。此外,在 CCA 组织和细胞系中证实 lncRNA PVT1 和 KLF5 高度表达。沉默和过表达 lncRNA PVT1 或 KLF5 分别显著抑制和增加 CCA 细胞系中的细胞增殖和细胞侵袭。沉默和过表达 lncRNA PVT1 分别显著抑制和增加 CCA 细胞系中 KLF5 的表达。沉默 lncRNA PVT1 增加了 CCA 细胞系中 miR186 的表达,而沉默 miR186 增加了 KLF5 的表达。与对照相比,共转染 lncRNA PVT1 和 miR186 增加了 KLF5 的表达。总体而言,这些结果表明 lncRNA PVT1/miR186/KLF5 轴可能在 CCA 的发生和发展中发挥关键作用,该轴可能为治疗 CCA 提供新的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/0d90effd2566/BMRI2021-8893652.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/2aaf5b48943c/BMRI2021-8893652.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/94ebb29ceff6/BMRI2021-8893652.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/c14afa6f6051/BMRI2021-8893652.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/a52275dff892/BMRI2021-8893652.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/7f6bff769def/BMRI2021-8893652.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/8888712e53fb/BMRI2021-8893652.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/0d90effd2566/BMRI2021-8893652.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/2aaf5b48943c/BMRI2021-8893652.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/94ebb29ceff6/BMRI2021-8893652.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/c14afa6f6051/BMRI2021-8893652.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/a52275dff892/BMRI2021-8893652.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/7f6bff769def/BMRI2021-8893652.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/8888712e53fb/BMRI2021-8893652.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8a/8286192/0d90effd2566/BMRI2021-8893652.007.jpg

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本文引用的文献

1
The Advancement of Long Non-Coding RNAs in Cholangiocarcinoma Development.长链非编码RNA在胆管癌发生发展中的研究进展
J Cancer. 2019 May 26;10(11):2407-2414. doi: 10.7150/jca.32411. eCollection 2019.
2
Cellular functions of long noncoding RNAs.长非编码 RNA 的细胞功能。
Nat Cell Biol. 2019 May;21(5):542-551. doi: 10.1038/s41556-019-0311-8. Epub 2019 May 2.
3
Surgery for cholangiocarcinoma.胆管癌的外科治疗。
长链非编码RNA-PKD2-2-3/miR-328/GPAM竞争性内源RNA网络诱导胆管癌增殖、侵袭及5-氟尿嘧啶化疗耐药
Front Oncol. 2022 Jul 29;12:871281. doi: 10.3389/fonc.2022.871281. eCollection 2022.
Liver Int. 2019 May;39 Suppl 1(Suppl Suppl 1):143-155. doi: 10.1111/liv.14089.
4
Long Non-coding RNA PVT1 Promotes Cell Proliferation and Migration by Silencing ANGPTL4 Expression in Cholangiocarcinoma.长链非编码RNA PVT1通过沉默胆管癌中ANGPTL4的表达促进细胞增殖和迁移。
Mol Ther Nucleic Acids. 2018 Dec 7;13:503-513. doi: 10.1016/j.omtn.2018.10.001. Epub 2018 Oct 10.
5
Global identification and characterization of lncRNAs that control inflammation in malignant cholangiocytes.全球鉴定和表征控制恶性胆管细胞炎症的 lncRNAs。
BMC Genomics. 2018 Oct 11;19(1):735. doi: 10.1186/s12864-018-5133-8.
6
KLF5 promotes the tumorigenesis and metastatic potential of thyroid cancer cells through the NF-κB signaling pathway.KLF5 通过 NF-κB 信号通路促进甲状腺癌细胞的肿瘤发生和转移潜能。
Oncol Rep. 2018 Nov;40(5):2608-2618. doi: 10.3892/or.2018.6687. Epub 2018 Sep 6.
7
Expression Analysis of PVT1, CCDC26, and CCAT1 Long Noncoding RNAs in Acute Myeloid Leukemia Patients.急性髓系白血病患者中PVT1、CCDC26和CCAT1长链非编码RNA的表达分析
Genet Test Mol Biomarkers. 2018 Oct;22(10):593-598. doi: 10.1089/gtmb.2018.0143. Epub 2018 Sep 14.
8
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9
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Sci Rep. 2017 Nov 16;7(1):15683. doi: 10.1038/s41598-017-15979-1.
10
Emerging molecular therapeutic targets for cholangiocarcinoma.胆管癌的新兴分子治疗靶点。
J Hepatol. 2017 Sep;67(3):632-644. doi: 10.1016/j.jhep.2017.03.026. Epub 2017 Apr 5.