内科理论与实践 ›› 2021, Vol. 16 ›› Issue (02): 121-125.doi: 10.16138/j.1673-6087.2021.02.011

• 论著 • 上一篇    下一篇

胰腺癌血清微RNA-486-3p的异常表达及对细胞增殖、凋亡的影响

李晓丽1, 李为光2(), 钱爱华2, 曹国良1   

  1. 1.上海交通大学医学院附属第九人民医院老年病科,上海 200011
    2.上海交通大学医学院附属瑞金医院消化科,上海 200025
  • 收稿日期:2020-12-04 出版日期:2021-04-25 发布日期:2022-07-26
  • 通讯作者: 李为光 E-mail:liweiguang2006@126.com

The serum level of microRNA-486-3p and its effects on proliferation and apoptosis of pancreatic cancer cells

LI Xiaoli1, LI Weiguang2(), QIAN Aihua2, CAO Guoliang1   

  1. 1. Department of Geratology,Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200011, China
    2. Department of Gastroenterology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China
  • Received:2020-12-04 Online:2021-04-25 Published:2022-07-26
  • Contact: LI Weiguang E-mail:liweiguang2006@126.com

摘要:

目的:研究胰腺癌患者血清微RNA(microRNA,miRNA/miR)-486-3p的表达情况及其在体外实验中对人胰腺癌细胞增殖、凋亡的影响。方法:于消化科、胰腺外科及老年科病房收集确诊胰腺癌患者21例为试验组,20名健康成人为对照组,留取外周血并分离血清,实时定量聚合酶链反应(polymerase chain reaction,PCR)检测血清中miR-486-3p的表达水平;体外实验采用细胞计数试剂盒8(cell-counting kit 8,CCK-8)法和流式细胞仪分别检测miR-486-3p对人胰腺癌细胞增殖、细胞凋亡的影响。结果:与健康对照组相比,胰腺癌患者血清中miR-486-3p的表达水平明显升高(50.73±0.82比34.80±0.74,P<0.05); 体外实验中采用干扰小RNA(small interfering RNA,siRNA)瞬时转染的方法增高miR-486-3p的表达,使得人胰腺癌细胞SW1990和PANC-1的增殖能力明显增强(2.77±0.07比2.05±0.06,P<0.05;2.81±0.04比1.89±0.04,P<0.05);抑制miR-486-3p则可明显减少胰腺癌细胞的增殖(1.71±0.03比2.07±0.05,P<0.05;1.61±0.03比2.20±0.07,P<0.05);增高miR-486-3p的表达可明显减少细胞凋亡(24.1%±1.14%比45.9%±1.11%,P<0.05;21.9%±0.25%比42.3%±1.62%,P<0.05)。结论:胰腺癌患者血清中miR-486-3p较健康对照组明显升高,可促进胰腺癌细胞的增殖并抑制细胞凋亡而发挥促癌作用。

关键词: 胰腺癌, 血清微RNA-486-3p, 细胞增殖和凋亡

Abstract:

Objective To investigate the serum level of microRNA-486-3p (miR-486-3p) and its effects on proliferation and apoptosis of pancreatic cancer cells. Methods Twenty-one patients with pancreatic cancer and twenty healthy controls were enrolled. Real-time polymerase chain reaction(PCR) was used to detect the serum miR-486-3p. The effects of miR-486-3p on pancreatic cancer cells proliferation and apoptosis were respectively examined by cell counting kit 8(CCK8) assay and flow cytometry assay. Results Compared with healthy controls,serum level of miR-486-3p was significantly up-regulated in patients with pancreatic cancer (50.73±0.82 vs 34.80±0.74, P<0.05); The proliferation of pancreatic cancer cells were significantly up-regulated (SW1990: 2.77±0.07 vs 2.05±0.06, P<0.05; PANC-1: 2.81±0.04 vs1.89±0.04, P<0.05) and the apoptosis rates were suppressed by forced expression of miR-486-3p(24.1%±1.14% vs 45.9%±1.11%, P<0.05; 21.9%±0.25% vs 42.3%±1.62%, P<0.05), while inhibition of miR-486-3p significantly down-regulated the proliferation of pancreatic cancer cells(SW1990: 1.71±0.03 vs 2.07±0.05, P<0.05; PANC-1: 1.61±0.03 vs 2.20±0.07, P<0.05). Conclusions The serum miR-486-3p were significantly up-regulated in patients with pancreatic cancer; MiR-486-3p may function as a tumor-promoter by promoting cell proliferation and suppressing apoptosis in pancreatic cancer cells.

Key words: Pancreatic cancer, Serum microRNA-486-3p, Cell proliferation and apoptosis

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