Chen Bin, Yu Jing, Wang Qianqian, Zhao Yuanyuan, Sun Li, Xu Changgen, Zhao Xiangdong, Shen Bo, Wang Mei, Xu Wenrong, Zhu Wei
School of Medicine, Jiangsu University, Zhenjiang, Jiangsu, China.
The Xuyi People's Hospital, Xuyi, Jiangsu, China.
Stem Cells Int. 2018 Jul 18;2018:9501747. doi: 10.1155/2018/9501747. eCollection 2018.
The clinical application of human bone marrow mesenchymal stem cells (hBM-MSCs) has generated a great deal of interest because of their potential use in regenerative medicine and tissue engineering. However, safety concerns over hBM-MSCs limit their clinical application. In this study, we observed that hBM-MSC-conditioned medium (hBM-MSC-CM) promotes gastric cancer development via upregulation of c-Myc. Our results showed that c-Myc was upregulated in MGC-803 and BGC-823 cells after hBM-MSC-CM treatment. Moreover, we found that the c-Myc inhibitor JQ1 and c-Myc siRNA decreased the expression of c-Myc in hBM-MSC-CM-treated tumor cells . Additionally, hBM-MSC-CM enhanced the migration and glucose uptake of gastric cancer cells. studies showed that JQ1 inhibited hBM-MSC-CM-induced gastric cancer growth. These results indicated that hBM-MSC-CM induced gastric cancer growth via upregulation of c-Myc, which may be a potential risk factor and/or a therapeutic target for clinical applications.
人骨髓间充质干细胞(hBM-MSCs)因其在再生医学和组织工程中的潜在应用而在临床应用方面引起了广泛关注。然而,对hBM-MSCs的安全性担忧限制了它们的临床应用。在本研究中,我们观察到hBM-MSC条件培养基(hBM-MSC-CM)通过上调c-Myc促进胃癌发展。我们的结果表明,hBM-MSC-CM处理后,MGC-803和BGC-823细胞中的c-Myc上调。此外,我们发现c-Myc抑制剂JQ1和c-Myc siRNA降低了hBM-MSC-CM处理的肿瘤细胞中c-Myc的表达。此外,hBM-MSC-CM增强了胃癌细胞的迁移和葡萄糖摄取。研究表明,JQ1抑制hBM-MSC-CM诱导的胃癌生长。这些结果表明,hBM-MSC-CM通过上调c-Myc诱导胃癌生长,这可能是临床应用中的潜在危险因素和/或治疗靶点。