Department of Surgical Oncology and General Surgery, The First Hospital of China Medical University, Shenyang, China.
Department of Thoracic Surgery, The First Hospital of China Medical University, Shenyang, China.
J Cell Physiol. 2019 Apr;234(4):4515-4527. doi: 10.1002/jcp.27269. Epub 2018 Sep 7.
Recent research suggests that the first-line oral antidiabetes drug metformin may prevent gastric cancer progression and improve prognosis. Many studies have also shown that long noncoding RNAs (lncRNAs) play important roles in many biological processes. Therefore, we aimed to explore whether lncRNAs participate in the mechanisms by which metformin affects gastric cancer cells. In the current study, we found that metformin significantly inhibited the cellular functions of gastric cancer cells through Cell Counting Kit-8 and invasion assays. We found that lncRNA H19 was greatly downregulated in gastric cancer cells treated with metformin using lncRNA microassays. Based on bioinformatics analyses of the Oncomine and The Cancer Genome Atlas databases, H19 is shown to be overexpressed in gastric cancer tissues, with increased expression of H19 relating to advanced pathological tumor stage and pathological tumor node metastasis stage, indicating that H19 may be associated with the invasive ability of gastric cancer. We knocked down H19 in AGS and SGC7901 cell lines and found that knocked-down H19 could decrease gastric cancer cell invasion and that metformin could not further decrease invasion after the knock down. Moreover, H19 depletion increased AMPK activation and decreased MMP9 expression, and metformin could not further activate AMPK or decrease MMP9 in H19 knocked-down gastric cancer cells. In summary, metformin has a profound antitumor effect on gastric cancer cells, and H19 is a key component in the process of metformin suppressing gastric cancer cell invasion.
最近的研究表明,一线口服降糖药二甲双胍可能预防胃癌进展并改善预后。许多研究还表明,长链非编码 RNA(lncRNA)在许多生物学过程中发挥重要作用。因此,我们旨在探讨 lncRNA 是否参与二甲双胍影响胃癌细胞的机制。在本研究中,我们发现二甲双胍通过细胞计数试剂盒-8 和侵袭实验显著抑制胃癌细胞的细胞功能。通过 lncRNA 微阵列实验,我们发现二甲双胍处理的胃癌细胞中 lncRNA H19 显著下调。基于 Oncomine 和癌症基因组图谱数据库的生物信息学分析,H19 在胃癌组织中表达上调,H19 的表达增加与晚期病理肿瘤分期和病理肿瘤淋巴结转移分期相关,表明 H19 可能与胃癌的侵袭能力相关。我们在 AGS 和 SGC7901 细胞系中敲低 H19,发现敲低 H19 可降低胃癌细胞侵袭,且敲低后二甲双胍不能进一步降低侵袭。此外,H19 耗竭可增加 AMPK 激活并降低 MMP9 表达,且 H19 敲低的胃癌细胞中二甲双胍不能进一步激活 AMPK 或降低 MMP9。综上所述,二甲双胍对胃癌细胞具有深刻的抗肿瘤作用,H19 是二甲双胍抑制胃癌细胞侵袭过程中的关键组成部分。