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miR-449 靶向调控 Flot2 作为胶质瘤的预后标志物

Flot2 targeted by miR-449 acts as a prognostic biomarker in glioma.

机构信息

a Department of Neurosurgery , Fujian Provincial Hospital of Fujian Medical University , Fuzhou , China.

b Department of Pathology , Fujian Provincial Hospital of Fujian Medical University , Fuzhou , China.

出版信息

Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):250-255. doi: 10.1080/21691401.2018.1549062.

DOI:10.1080/21691401.2018.1549062
PMID:30663389
Abstract

Flotillin-2 (FLOT2) was reported as oncogene and involves in the pathogenic process of several cancers, yet the precise mechanism of FLOT2 in glioma is still limited. In this study, we demonstrated that FLOT2 expression levels were greatly upregulated in glioma tissues and cell lines, and the FLOT2 expression in glioma tissue was markedly associated with tumour stage and size. Overexpression of FLOT2 was correlated with poor prognosis of glioma patients. The functional assay revealed that silenced FLOT2 repressed the viability, migration, and invasion of glioma cells. And then, we detected the relationship between miR-449 and FLOT2. Luciferase reporter assay and Western blot results showed that miR-449 directly binding the 3'UTR sequence of FLOT2 and regulated FLOT2 expression in glioma cells. Finally, we detected the expression levels of miR-449 in glioma tissue and cell lines and found that miR-449 was significantly downregulated in glioma tissues and cell lines. In conclusion, we demonstrated that overexpression FLOT2 was associated with poor prognosis of glioma patients and involved in the progression of glioma, identifying a novel prognostic biomarker and therapeutic target for glioma progression.

摘要

flotillin-2 (FLOT2) 被报道为癌基因,参与了几种癌症的发病过程,然而,FLOT2 在神经胶质瘤中的精确机制仍有限。在本研究中,我们证明了 FLOT2 在神经胶质瘤组织和细胞系中的表达水平显著上调,FLOT2 在神经胶质瘤组织中的表达与肿瘤分期和大小明显相关。FLOT2 的过表达与神经胶质瘤患者的不良预后相关。功能分析表明,沉默 FLOT2 抑制了神经胶质瘤细胞的活力、迁移和侵袭。然后,我们检测了 miR-449 和 FLOT2 之间的关系。荧光素酶报告基因检测和 Western blot 结果表明,miR-449 可以直接结合 FLOT2 的 3'UTR 序列并调节神经胶质瘤细胞中的 FLOT2 表达。最后,我们检测了神经胶质瘤组织和细胞系中 miR-449 的表达水平,发现 miR-449 在神经胶质瘤组织和细胞系中显著下调。总之,我们证明了高表达的 FLOT2 与神经胶质瘤患者的不良预后相关,并参与了神经胶质瘤的进展,确定了一个新的预后生物标志物和神经胶质瘤进展的治疗靶点。

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Flot2 targeted by miR-449 acts as a prognostic biomarker in glioma.miR-449 靶向调控 Flot2 作为胶质瘤的预后标志物
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FLOT2 upregulation promotes growth and invasion by interacting and stabilizing EphA2 in gliomas.FLOT2 上调通过与 EphA2 相互作用和稳定 EphA2 促进胶质瘤的生长和侵袭。
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引用本文的文献

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Front Oncol. 2022 Nov 8;12:1030366. doi: 10.3389/fonc.2022.1030366. eCollection 2022.
2
Long non-coding RNA MIR4435-2HG: a key molecule in progression of cancer and non-cancerous disorders.长链非编码RNA MIR4435-2HG:癌症和非癌症疾病进展中的关键分子。
Cancer Cell Int. 2022 Jun 17;22(1):215. doi: 10.1186/s12935-022-02633-8.
3
TBL1X and Flot2 form a positive feedback loop to promote metastasis in nasopharyngeal carcinoma.
TBL1X 和 Flot2 形成正反馈环促进鼻咽癌转移。
Int J Biol Sci. 2022 Jan 1;18(3):1134-1149. doi: 10.7150/ijbs.68091. eCollection 2022.
4
A Novel Prognostic Tool for Glioma Based on Enhancer RNA-Regulated Immune Genes.一种基于增强子RNA调控免疫基因的新型胶质瘤预后评估工具。
Front Cell Dev Biol. 2022 Jan 20;9:798445. doi: 10.3389/fcell.2021.798445. eCollection 2021.
5
miR-363-3p induces EMT via the Wnt/β-catenin pathway in glioma cells by targeting CELF2.miR-363-3p 通过靶向 CELF2 诱导胶质瘤细胞中的 EMT 发生,该过程涉及 Wnt/β-catenin 通路。
J Cell Mol Med. 2021 Nov;25(22):10418-10429. doi: 10.1111/jcmm.16970. Epub 2021 Oct 12.
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miR-299-3p suppresses cell progression and induces apoptosis by downregulating PAX3 in gastric cancer.微小RNA-299-3p通过下调胃癌中的PAX3抑制细胞进展并诱导细胞凋亡。
Open Life Sci. 2021 Mar 23;16(1):266-276. doi: 10.1515/biol-2021-0022. eCollection 2021.
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Long non-coding RNA SNHG3 accelerates progression in glioma by modulating miR-384/HDGF axis.长链非编码RNA SNHG3通过调控miR-384/HDGF轴促进胶质瘤进展。
Open Life Sci. 2020 Sep 5;15(1):654-664. doi: 10.1515/biol-2020-0066. eCollection 2020.
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Open Life Sci. 2020 Jul 10;15(1):476-487. doi: 10.1515/biol-2020-0050. eCollection 2020.
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