MicroRNA‑1224 inhibits cell proliferation by downregulating CBX3 expression in chordoma.

IF 2.5 4区 医学 Q3 ONCOLOGY
Wei Xia, Jihe Huang, Chunhua Sun, Fei Shen, Kejia Yang
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引用次数: 0

Abstract

MicroRNAs (miRNAs/miRs) have abnormal expression in numerous tumors and are closely related to tumor development and resistance to radiotherapy and chemotherapy. However, there are few studies assessing the role and mechanism of miRNA in chordoma. The sequencing data of three pairs of chordoma and notochord tissues from the GSE56183 dataset were analyzed in the present study. Cell proliferation was assessed in vitro using Cell Counting Kit-8. Bioinformatics analysis and the dual luciferase reporter assay were used to evaluate the regulatory relationship between miR-1224 and chromobox 3 (CBX3) in chordoma. The results demonstrated that miR-1224 had a significantly lower expression level in chordoma tissues and cell lines. Overexpression of miR-1224 inhibited proliferation in the chordoma cells, while the knockdown of miR-1224 promoted proliferation of the chordoma cells. Bioinformatics analysis and the dual luciferase reporter assay confirmed that CBX3 was a direct target gene of miR-1224 and that miR-1224 induced the proliferation of chordoma cells through the inhibition of CBX3. In summary, miR-1224 reduced the proliferation of chordoma cells through inhibition of CBX3, which provides a theoretical basis for selecting a novel therapeutic target for chordoma.
MicroRNA-1224 通过下调脊索瘤中 CBX3 的表达抑制细胞增殖。
微小RNA(miRNA/miRs)在许多肿瘤中都有异常表达,与肿瘤发生发展以及对放疗和化疗的耐受性密切相关。然而,很少有研究评估 miRNA 在脊索瘤中的作用和机制。本研究分析了 GSE56183 数据集中三对脊索瘤和非脊索组织的测序数据。使用细胞计数试剂盒-8在体外评估细胞增殖。生物信息学分析和双荧光素酶报告实验被用来评估脊索瘤中 miR-1224 和 chromobox 3 (CBX3) 之间的调控关系。结果表明,miR-1224在脊索瘤组织和细胞系中的表达水平明显较低。过表达 miR-1224 会抑制脊索瘤细胞的增殖,而敲除 miR-1224 则会促进脊索瘤细胞的增殖。生物信息学分析和双荧光素酶报告实验证实,CBX3是miR-1224的直接靶基因,miR-1224通过抑制CBX3诱导脊索瘤细胞增殖。综上所述,miR-1224通过抑制CBX3减少了脊索瘤细胞的增殖,为选择脊索瘤的新型治疗靶点提供了理论依据。
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来源期刊
Oncology Letters
Oncology Letters ONCOLOGY-
CiteScore
5.70
自引率
0.00%
发文量
412
审稿时长
2.0 months
期刊介绍: Oncology Letters is a monthly, peer-reviewed journal, available in print and online, that focuses on all aspects of clinical oncology, as well as in vitro and in vivo experimental model systems relevant to the mechanisms of disease. The principal aim of Oncology Letters is to provide the prompt publication of original studies of high quality that pertain to clinical oncology, chemotherapy, oncogenes, carcinogenesis, metastasis, epidemiology and viral oncology in the form of original research, reviews and case reports.
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