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长链非编码RNA父源表达印记基因10(PEG10)通过靶向miR-101-3p调控驱动蛋白家族成员2A(KIF2A)来促进弥漫性大B细胞淋巴瘤进展。

Long Non-Coding RNA Paternally Expressed Imprinted Gene 10 (PEG10) Elevates Diffuse Large B-Cell Lymphoma Progression by Regulating Kinesin Family Member 2A (KIF2A) via Targeting MiR-101-3p.

作者信息

Zhao Jin, Su Liping, Jiang Jianjun

机构信息

Department of Hematology, Affiliated Shanxi Tumor Hospital of Shanxi Medical University, Taiyuan, Shanxi, China (mainland).

Department of Palliative Medicine, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, China (mainland).

出版信息

Med Sci Monit. 2020 Sep 25;26:e922810. doi: 10.12659/MSM.922810.

Abstract

BACKGROUND Diffuse large B-cell lymphoma (DLBCL) is a common malignant tumor in the immune system with high mortality. We investigated the functional effects of long non-coding RNA paternally expressed imprinted gene 10 (PEG10) on DLBCL progression. MATERIAL AND METHODS Real-time quantitative polymerase chain reaction was used to measure the level of PEG10, kinesin family member 2A (KIF2A) and microRNA-101-3p (miR-101-3p) in DLBCL tissues and cell lines. The relative protein level was detected by western blot analysis. The biological behaviors including cell proliferation, apoptosis, migration, and invasion were determined by MTT assay, flow cytometry analysis, and Transwell assays, respectively. Bioinformatics analysis and dual-luciferase reporter assay were performed to evaluate the interaction among PEG10, miR-101-3p, and KIF2A. RESULTS PEG10 and KIF2A level were significantly upregulated, while miR-101-3p was downregulated in DLBCL tissues and cells. PEG10 positively regulated KIF2A level in DLBCL. PEG10, or KIF2A deletion significantly inhibited the proliferative, migratory, and invasive abilities of DLBCL cells and elevated cell apoptosis in DLBCL cells. KIF2A upregulation partially reversed the effects of PEG10 downregulation on cell growth, metastasis, and apoptosis in DLBCL. Moreover, PEG10 negatively regulated miR-101-3p level and miR-101-3p upregulation exerted inhibition effects on the progression of DLBCL. Besides, miR-101-3p was a target of PEG10 and miR-101-3p could directly target KIF2A. PEG10 promoted KIF2A level by sponging miR-101-3p. CONCLUSIONS Our findings revealed that PEG10 played an oncogenic role in DLBCL progression, which might be a potential target for the treatment of DLBCL.

摘要

背景 弥漫性大B细胞淋巴瘤(DLBCL)是免疫系统中一种常见的恶性肿瘤,死亡率很高。我们研究了长链非编码RNA父源表达印记基因10(PEG10)对DLBCL进展的功能影响。

材料与方法 采用实时定量聚合酶链反应检测DLBCL组织和细胞系中PEG10、驱动蛋白家族成员2A(KIF2A)和微小RNA-101-3p(miR-101-3p)的水平。通过蛋白质印迹分析检测相对蛋白水平。分别通过MTT法、流式细胞术分析和Transwell实验测定细胞增殖、凋亡、迁移和侵袭等生物学行为。进行生物信息学分析和双荧光素酶报告基因实验以评估PEG10、miR-101-3p和KIF2A之间的相互作用。

结果 在DLBCL组织和细胞中,PEG10和KIF2A水平显著上调,而miR-101-3p水平下调。PEG10在DLBCL中正向调节KIF2A水平。PEG10或KIF2A缺失显著抑制DLBCL细胞的增殖、迁移和侵袭能力,并增加DLBCL细胞的凋亡。KIF2A上调部分逆转了PEG10下调对DLBCL细胞生长、转移和凋亡的影响。此外,PEG10负向调节miR-101-3p水平,miR-101-3p上调对DLBCL进展具有抑制作用。此外,miR-101-3p是PEG10的靶标,miR-101-3p可直接靶向KIF2A。PEG10通过吸附miR-101-3p促进KIF2A水平升高。

结论 我们的研究结果表明,PEG10在DLBCL进展中发挥致癌作用,可能是DLBCL治疗的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11e7/7523416/cf55a278d037/medscimonit-26-e922810-g001.jpg

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