基础医学与临床 ›› 2024, Vol. 44 ›› Issue (1): 8-15.doi: 10.16352/j.issn.1001-6325.2024.01.0008

• 研究论文 • 上一篇    下一篇

miR-139-5p增强二甲双胍抑制正常糖培养下人胰腺癌细胞系PANC-1增殖

余洁1#, 马明磊2#, 张化冰1, 平凡1, 李伟1, 许岭翎1, 李玉秀1*   

  1. 1.中国医学科学院 北京协和医学院 北京协和医院 内分泌科 国家卫生健康委员会内分泌重点实验室,北京 100730;
    2.首都医科大学附属北京世纪坛医院 内分泌科,北京 100038
  • 收稿日期:2023-05-17 修回日期:2023-11-30 出版日期:2024-01-05 发布日期:2023-12-25
  • 通讯作者: *:liyuxiu@medmail.com.cn
  • 作者简介:#对本文有相同贡献
  • 基金资助:
    国家自然科学基金(82100947);中国医学科学院医学与健康科技创新工程(CIFMS2021-I2M-1-002)

miR-139-5p enhances the inhibition effect of metformin on cell proliferation of pancreatic cancer cell line PANC-1 cultured in normal-glucose medium

YU Jie1#, MA Minglei2#, ZHANG Huabing1, PING Fan1, LI Wei1, XU Lingling1, LI Yuxiu1*   

  1. 1. Department of Endocrinology, Key Laboratory of Endocrinology of National Health Commission, Peking Union Medical College Hospital, CAMS & PUMC, Beijing 100730;
    2. Department of Endocrinology, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China
  • Received:2023-05-17 Revised:2023-11-30 Online:2024-01-05 Published:2023-12-25
  • Contact: *:liyuxiu@medmail.com.cn

摘要: 目的 研究不同葡萄糖浓度培养条件下,二甲双胍(Met)对人胰腺癌细胞系PANC-1增殖的影响,并确定miR-139-5p是否参与此过程。方法 采用梯度浓度的二甲双胍(0、5、10、20 mmol/L)分别在25 mmol/L葡萄糖[高糖(HG)组]或5 mmol/L葡萄糖[正常糖(NG)组]培养条件下处理PANC-1细胞。培养48 h后,检测细胞的增殖、凋亡、迁移及细胞周期。通过RT-qPCR检测miR-139-5p的表达情况,同时将miR-139-5p模拟物转染到PANC-1细胞中以明确其作用。结果 无论是在HG,还是NG培养条件下,二甲双胍均可抑制PANC-1细胞的增殖、促进细胞凋亡(P<0.05),并诱导细胞周期阻滞在S期和G2/M期(P<0.05)。在NG培养条件下,二甲双胍的抗增殖和促凋亡作用更显著(P<0.05)。此外,仅在NG培养条件下,二甲双胍使miR-139-5p的表达上调(P<0.001),且miR-139-5p模拟物可以抑制该培养条件下无二甲双胍干预下PANC-1细胞的增殖(P<0.05),并增强5 mmol/L二甲双胍的抗增殖作用和10 mmol/L二甲双胍的促凋亡作用(P<0.05)。结论 在正常糖培养条件下,二甲双胍对PANC-1细胞增殖的抑制、对细胞凋亡的诱导以及细胞周期阻滞作用均较高糖培养条件下更为显著。这些作用部分可能与上调miR-139-5p有关。

关键词: 胰腺癌, 二甲双胍, 葡萄糖, 微RNA, miR-139-5p

Abstract: Objective To investigate the effects of metformin(Met) on the proliferation of pancreatic cancer cells under different glucose concentration culture conditions, and to find the potential role of miR-139-5p in the process. Methods PANC-1 cells were treated with different concentrations of metformin(0/5/10/20 mmol/L) in 25 mmol/L(high-glucose group,HG) or 5 mmol/L(normal-glucose group,NG) glucose culture, cell proliferation, apoptosis, migration and cell cycle were detected after 48 h. The expression of miR-139-5p was quantitatively detected by RT-qPCR, and the miR-139-5p mimics were transfected into PANC-1 cells to clarify the role of miR-139-5p. Results Metformin inhibited the proliferation, promoted apoptosis, and induced S phase and G2/M phase arrest of PANC-1 cells under in high glucose and normal glucose culture conditions, and its anti-proliferation and pro-apoptosis effects were more significant in the normal glucose groups. The expression of miR-139-5p was up-regulated by metformin treatment in normal but not in high glucose culture. Further studies showed that miR-139-5p mimics inhibited of PANC-1 cells proliferation without metformin pre-incubation and enhanced the anti-proliferation effect of 5 mmol/L metformin. The pro-apoptotic effect of 10 mmol/L metformin in normal glucose culture conditions. Conclusions In normal-glucose culture conditions, metformin can inhibit proliferation, induce apoptosis and cell cycle arrest of PANC-1 cells more significantly than in higher-glucose culture, which may be partly related to the up-regulation of miR-139-5p.

Key words: pancreatic cancer, metformin, glucose, microRNA, miR-139-5p

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