The effect of miR-381 on proliferation and prognosis of breast cancer by altering CCNA2 expression.

IF 0.9 4区 医学 Q4 OBSTETRICS & GYNECOLOGY
Journal of Obstetrics and Gynaecology Pub Date : 2024-12-01 Epub Date: 2024-06-21 DOI:10.1080/01443615.2024.2360547
Ming-Gang Cao, Yan Wang, Zhi-Min Yang, Yang Wang, Mei-Qing Wang, Shuai Zhuo, Yan Yang, Chun-Sheng Liu
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引用次数: 0

Abstract

Background: MiR-381 can regulate the expression of cyclin A2 (CCNA2) to inhibit the proliferation and migration of bladder cancer cells, but whether miR-381 has the same function in breast cancer is not well know.

Methods: The over express or silence miR-381 expressing cell lines were constructed by lentivirus infection to reveal the biological functions of miR-381 in vitro. The expression of miR-381 and CCNA2 in 162 breast cancer patients were detected to further reveal their impact and predictive value on progression-free survival (PFS) and overall survival (OS).

Results: After transfection of MDA-MB-231 and MCF-7 cells with miR-381 mimics, the expression of miR-381 was effectively up-regulated and CCNA2 was effectively down-regulated, while the opposite results were observed in tumour cell which transfected with miR-381 inhibitors. After transfection of cell lines with miR-381 mimics, tumour cell activity was significantly reduced, while the opposite results were observed in tumour cell which transfected with miR-381 inhibitors. The area under curves (AUCs) of miRNA-381 and CCNA2 for predicting PFS and OS were 0.711, 0.695, 0.694 and 0.675 respectively. Cox regression analysis showed that miRNA-381 ≥ 1.65 2-ΔΔCt and CCNA ≥ 2.95 2-ΔΔCt were the influence factors of PFS and OS, the hazard ratio (HR) values were 0.553, 2.075, 0.462 and 2.089, respectively.

Conclusion: miR-381 inhibitors breast cancer cells proliferation and migration by down-regulating the expression of CCNA2, both of them can predict the prognosis of breast cancer.

miR-381 通过改变 CCNA2 表达对乳腺癌增殖和预后的影响
背景:MiR-381可调控细胞周期蛋白A2(CCNA2)的表达,从而抑制膀胱癌细胞的增殖和迁移,但miR-381在乳腺癌中是否具有同样的功能尚不清楚:方法:为了揭示miR-381在体外的生物学功能,我们通过慢病毒感染构建了过度表达或沉默miR-381的细胞系。方法:通过慢病毒感染构建miR-381表达过量或沉默的细胞系,揭示miR-381在体外的生物学功能;检测162例乳腺癌患者体内miR-381和CCNA2的表达,进一步揭示其对无进展生存期(PFS)和总生存期(OS)的影响和预测价值:结果:用miR-381模拟物转染MDA-MB-231和MCF-7细胞后,miR-381的表达有效上调,CCNA2的表达有效下调,而转染miR-381抑制剂的肿瘤细胞则观察到相反的结果。用 miR-381 模拟物转染细胞系后,肿瘤细胞的活性明显降低,而转染了 miR-381 抑制剂的肿瘤细胞的活性则相反。miRNA-381和CCNA2预测PFS和OS的曲线下面积(AUC)分别为0.711、0.695、0.694和0.675。Cox回归分析表明,miRNA-381≥1.65 2-ΔΔCt和CCNA≥2.95 2-ΔΔCt是PFS和OS的影响因素,其危险比(HR)值分别为0.553、2.075、0.462和2.089。
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来源期刊
CiteScore
2.40
自引率
7.70%
发文量
398
审稿时长
6 months
期刊介绍: Journal of Obstetrics and Gynaecology represents an established forum for the entire field of obstetrics and gynaecology, publishing a broad range of original, peer-reviewed papers, from scientific and clinical research to reviews relevant to practice. It also includes occasional supplements on clinical symposia. The journal is read widely by trainees in our specialty and we acknowledge a major role in education in Obstetrics and Gynaecology. Past and present editors have recognized the difficulties that junior doctors encounter in achieving their first publications and spend time advising authors during their initial attempts at submission. The journal continues to attract a world-wide readership thanks to the emphasis on practical applicability and its excellent record of drawing on an international base of authors.
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