Kato Kiyohito, Iwama Hisakazu, Yamashita Takuma, Kobayashi Kiyoyuki, Fujihara Shintaro, Fujimori Takayuki, Kamada Hideki, Kobara Hideki, Masaki Tsutomu
Department of Gastroenterology and Neurology, Faculty of Medicine, Kagawa University, Kita-gun, Kagawa Prefecture 761-0793, Japan.
Life Science Research Center, Kagawa University, Kita-gun, Kagawa Prefecture 761-0793, Japan.
Oncol Rep. 2016 Mar;35(3):1582-92. doi: 10.3892/or.2015.4496. Epub 2015 Dec 17.
Recent studies suggest that metformin, which is a commonly used oral anti-hyperglycemic agent of the biguanide family, may reduce cancer risk and improve prognosis, yet the detailed mechanisms by which metformin affects various types of cancers, including pancreatic cancer, remain unknown. The aim of the present study was to evaluate the effects of metformin on human pancreatic cancer cell proliferation in vitro and in vivo, and to study microRNAs (miRNAs) associated with the antitumor effect of metformin. We used the human pancreatic cancer cell lines Panc1, PK1 and PK9 to study the effects of metformin on human pancreatic cancer cells. Athymic nude mice bearing xenograft tumors were treated with or without metformin. Tumor growth was recorded after 5 weeks, and the expression of cell cycle-related proteins was determined. In addition, we used miRNA microarray tips to explore the differences in the levels of miRNAs in Panc1 cells and xenograft tumors treated with metformin or without. Metformin inhibited the proliferation of Panc1, PK1 and PK9 cells in vitro. This inhibition was accompanied by a strong decrease in G1 cyclins (particularly in cyclin D1) and retinoblastoma protein (Rb) phosphorylation. In addition, metformin reduced the phosphorylation of epidermal growth factor receptor (EGFR), particularly the phosphorylation of EGFR at Tyr845, and insulin-like growth factor 1 receptor (IGF-1R) in vitro and in vivo. miRNA expression was markedly altered by the treatment with metformin in vitro and in vivo. Our results revealed that metformin inhibits human pancreatic cancer cell proliferation and tumor growth, possibly by suppressing the cell cycle-related molecules via alteration of miRNAs.
近期研究表明,二甲双胍作为双胍类家族常用的口服抗高血糖药物,可能降低癌症风险并改善预后,然而二甲双胍影响包括胰腺癌在内的各类癌症的具体机制仍不清楚。本研究的目的是评估二甲双胍在体外和体内对人胰腺癌细胞增殖的影响,并研究与二甲双胍抗肿瘤作用相关的微小RNA(miRNA)。我们使用人胰腺癌细胞系Panc1、PK1和PK9来研究二甲双胍对人胰腺癌细胞的影响。对携带异种移植瘤的无胸腺裸鼠进行有无二甲双胍的处理。5周后记录肿瘤生长情况,并测定细胞周期相关蛋白的表达。此外,我们使用miRNA微阵列芯片来探究经二甲双胍处理和未经处理的Panc1细胞及异种移植瘤中miRNA水平的差异。二甲双胍在体外抑制Panc1、PK1和PK9细胞的增殖。这种抑制伴随着G1期细胞周期蛋白(特别是细胞周期蛋白D1)和视网膜母细胞瘤蛋白(Rb)磷酸化的显著降低。此外,二甲双胍在体外和体内均降低了表皮生长因子受体(EGFR)的磷酸化,尤其是Tyr845位点的EGFR磷酸化,以及胰岛素样生长因子1受体(IGF-1R)的磷酸化。在体外和体内,二甲双胍处理均显著改变了miRNA的表达。我们的结果显示,二甲双胍可能通过改变miRNA来抑制细胞周期相关分子,从而抑制人胰腺癌细胞的增殖和肿瘤生长。