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J Cell Physiol. 2020 Oct;235(10):7194-7203. doi: 10.1002/jcp.29618. Epub 2020 Feb 10.
2
Selenium-mediated gga-miR-29a-3p regulates LMH cell proliferation, invasion, and migration by targeting COL4A2.硒介导的 gga-miR-29a-3p 通过靶向 COL4A2 调节 LMH 细胞的增殖、侵袭和迁移。
Metallomics. 2020 Mar 25;12(3):449-459. doi: 10.1039/c9mt00266a.
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MiR-645 promotes invasiveness, metastasis and tumor growth in colorectal cancer by targeting EFNA5.miR-645 通过靶向 EFNA5 促进结直肠癌的侵袭、转移和肿瘤生长。
Biomed Pharmacother. 2020 May;125:109889. doi: 10.1016/j.biopha.2020.109889. Epub 2020 Feb 6.
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Long non‑coding RNA GAS5 increases the radiosensitivity of A549 cells through interaction with the miR‑21/PTEN/Akt axis.长链非编码RNA GAS5通过与miR-21/PTEN/Akt轴相互作用增加A549细胞的放射敏感性。
Oncol Rep. 2020 Mar;43(3):897-907. doi: 10.3892/or.2020.7467. Epub 2020 Jan 15.
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MiRNA-200a-3p suppresses the proliferation, migration and invasion of non-small cell lung cancer through targeting IRS2.miRNA-200a-3p 通过靶向 IRS2 抑制非小细胞肺癌的增殖、迁移和侵袭。
Eur Rev Med Pharmacol Sci. 2020 Jan;24(2):712-720. doi: 10.26355/eurrev_202001_20050.
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Upregulation of LINC00504 is associated with aggressive progression and poor prognosis in non-small cell lung cancer.LINC00504 的上调与非小细胞肺癌的侵袭性进展和不良预后相关。
Eur Rev Med Pharmacol Sci. 2020 Jan;24(2):699-703. doi: 10.26355/eurrev_202001_20047.
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Up-regulated LINC01234 promotes non-small-cell lung cancer cell metastasis by activating VAV3 and repressing BTG2 expression.上调 LINC01234 通过激活 VAV3 和抑制 BTG2 表达促进非小细胞肺癌细胞转移。
J Hematol Oncol. 2020 Jan 20;13(1):7. doi: 10.1186/s13045-019-0842-2.
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LncRNA NNT-AS1 promotes non-small cell lung cancer progression through regulating miR-22-3p/YAP1 axis.长链非编码 RNA NNT-AS1 通过调控 miR-22-3p/YAP1 轴促进非小细胞肺癌进展。
Thorac Cancer. 2020 Mar;11(3):549-560. doi: 10.1111/1759-7714.13280. Epub 2020 Jan 10.
9
MicroRNA-1296 expression is associated with prognosis and inhibits cell proliferation and invasion by Wnt signaling in non-small cell lung cancer.微小RNA-1296的表达与非小细胞肺癌的预后相关,并通过Wnt信号通路抑制细胞增殖和侵袭。
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10
miR-512-5p suppresses the progression of non-small cell lung cancer by targeting β-catenin.微小RNA-512-5p通过靶向β-连环蛋白抑制非小细胞肺癌的进展。
Oncol Lett. 2020 Jan;19(1):415-423. doi: 10.3892/ol.2019.11102. Epub 2019 Nov 14.

沉默LINC00504可通过上调miR-876-3p抑制肺癌细胞的增殖、侵袭及迁移,并促进其凋亡。

Silencing LINC00504 inhibits cell proliferation, invasion as well as migration and promotes cell apoptosis in lung cancer cells via upregulating miR-876-3p.

作者信息

Zhang Zhen

机构信息

Cardiovascular thoracic surgery, Fu Yang People's Hospital, No. 501 Sanqing road, Yingzhou district, Fuyang, 236000, Anhui, China.

出版信息

Cytotechnology. 2020 Oct 8;72(6):807-17. doi: 10.1007/s10616-020-00424-5.

DOI:10.1007/s10616-020-00424-5
PMID:33033968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7695783/
Abstract

LINC00504 acts as an oncogene and associates with unfavorable prognosis in patients with lung cancer. Silencing LINC00504 may be a promising strategy for treatment of lung cancer and its effects were firstly investigated in lung cancer cells this study. The gene expression level of miR-876-3p as well as LINC00504 were measured via PCR assay. The cell proliferation was investigated through Cell Counting Kit-8 (CCK-8) assay and colony formation assay. Flow cytometry was applied for detection of cell apoptosis. Wound healing and transwell assay were performed for measurement of cell migration and invasion respectively. The apoptosis related protein expressions were measured by western blot. Luciferase report assay was conducted for verification the target gene. LINC00504 was higher expressed in five types of lung cancer cells studied herein when compared with the control normal cells. LINC00504 knockdown exerted inhibitory effects on cell apoptosis, cell migration as well as cell invasion and promoted cell apoptosis. All the effects mentioned above were counteracted by miR-876-3p inhibitor. Silencing LINC00504 possessed anti-proliferation, repression of cell invasion as well as migration and pro-apoptosis effects via targeting up-regulation of miR-876-3p in lung cancer cells, proving the new therapeutic targets and highlighting the potential application in future diagnosis and treatment in lung cancer.

摘要

LINC00504作为一种癌基因,与肺癌患者的不良预后相关。沉默LINC00504可能是一种有前景的肺癌治疗策略,本研究首次在肺癌细胞中研究了其作用效果。通过PCR检测法测定miR-876-3p以及LINC00504的基因表达水平。通过细胞计数试剂盒-8(CCK-8)检测法和集落形成检测法研究细胞增殖情况。应用流式细胞术检测细胞凋亡。分别采用伤口愈合检测法和Transwell检测法测量细胞迁移和侵袭能力。通过蛋白质免疫印迹法检测凋亡相关蛋白的表达。进行荧光素酶报告基因检测以验证靶基因。与对照正常细胞相比,LINC00504在本文研究的五种肺癌细胞中表达较高。敲低LINC00504对细胞凋亡、细胞迁移以及细胞侵袭均有抑制作用,并促进细胞凋亡。上述所有作用均被miR-876-3p抑制剂抵消。在肺癌细胞中,沉默LINC00504通过靶向上调miR-876-3p具有抗增殖、抑制细胞侵袭和迁移以及促凋亡作用,为肺癌提供了新的治疗靶点,并突出了其在未来肺癌诊断和治疗中的潜在应用价值。