Tseng Hui-Hwa, Chen You-Zuo, Chou Nan-Hua, Chen Yen-Chih, Wu Chao-Chuan, Liu Li-Feng, Yang Yi-Fang, Yeh Chung-Yu, Kung Mei-Lang, Tu Ya-Ting, Tsai Kuo-Wang
Division of Anatomic Pathology, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 23124, Taiwan.
Department of Medical Education and Research, Kaohsiung Veterans General Hospital, Kaohsiung 81362, Taiwan.
Mol Ther Oncolytics. 2021 Aug 19;22:180-194. doi: 10.1016/j.omto.2021.08.006. eCollection 2021 Sep 24.
Long noncoding RNAs (lncRNAs) are a group of nonprotein coding transcripts that play a critical role in cancer progression. However, the role of lncRNA in metformin-induced inhibition of cell growth and its biological function in gastric cancer remain largely unknown. In this study, we identified an oncogenic lncRNA, Loc100506691, the expression of which was decreased in gastric cancer cells with metformin treatment. Moreover, Loc100506691 was significantly overexpressed in gastric cancer compared with adjacent normal tissues (p < 0.001), and high Loc100506691 expression was significantly correlated with poor survival of patients with gastric cancer. Additionally, Loc100506691 knockdown could significantly suppress gastric cancer cell growth , and ectopic Loc100506691 expression accelerated tumor growth in an mouse model. Analysis of the cell cycle revealed that Loc100506691 knockdown induced cell cycle arrest at the G2/M phase by impairing cell entry from the G2/M to G1 phase. Loc100506691 negatively regulated CHAC1 expression by modulating miR-26a-5p/miR-330-5p expression, and CHAC1 knockdown markedly attenuated Loc100506691 knockdown-induced gastric cancer cell growth and motility suppression. We concluded that anti-proliferative effects of metformin in gastric cancer may be partially caused by suppression of the Loc100506691-miR-26a-5p/miR-330-5p-CHAC1 axis.
长链非编码RNA(lncRNAs)是一类非蛋白质编码转录本,在癌症进展中起关键作用。然而,lncRNA在二甲双胍诱导的细胞生长抑制中的作用及其在胃癌中的生物学功能仍 largely未知。在本研究中,我们鉴定出一种致癌lncRNA,即Loc100506691,在接受二甲双胍治疗的胃癌细胞中其表达降低。此外,与相邻正常组织相比,Loc100506691在胃癌中显著过表达(p < 0.001),且Loc100506691高表达与胃癌患者的不良生存显著相关。此外,敲低Loc100506691可显著抑制胃癌细胞生长,而异位表达Loc100506691可加速小鼠模型中的肿瘤生长。细胞周期分析显示,敲低Loc100506691通过损害细胞从G2/M期进入G1期诱导细胞周期停滞在G2/M期。Loc100506691通过调节miR-26a-5p/miR-330-5p的表达负向调节CHAC1的表达,敲低CHAC1可显著减弱敲低Loc100506691诱导的胃癌细胞生长和运动抑制。我们得出结论,二甲双胍在胃癌中的抗增殖作用可能部分是由抑制Loc100506691-miR-26a-5p/miR-330-5p-CHAC1轴引起的。