Huang Yao, Liu Wei, He Bing, Wang Lei, Zhang Fucheng, Shu Hao, Sun Luning
Department of Sports Medicine Center, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210029, China.
Department of Orthopaedics, the First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, China.
J Bone Oncol. 2020 Feb 4;21:100280. doi: 10.1016/j.jbo.2020.100280. eCollection 2020 Apr.
Osteosarcoma (OS) is a malignant bone tumor that frequently occurs in adolescents. It has a high rate of pulmonary metastasis and mortality. Previous studies have demonstrated that human bone marrow mesenchymal stem cells (hBMSCs) can promote the malignant progression in various tumors, including OS. Also, it is recognized that exosomes derived from hBMSCs (hBMSC-Exos) mediate cell-to-cell communication and exhibit similar effects on the development of various tumors. However, the role of hBMSC-Exos in the development of OS is still unclear and the underlying mechanism needs to be elucidated. Our results show that hBMSC-derived exosomes promote OS cell proliferation, migration, and invasion. Meanwhile, silencing autophagy-related gene 5 (ATG5) in OS cells abolishes the pro-tumor effects of hBMSC-Exos and Our present study demonstrates that hBMSC-Exos promotes tumorigenesis and metastasis by promoting oncogenic autophagy in OS.
骨肉瘤(OS)是一种常见于青少年的恶性骨肿瘤。它具有较高的肺转移率和死亡率。先前的研究表明,人骨髓间充质干细胞(hBMSCs)可促进包括OS在内的多种肿瘤的恶性进展。此外,人们认识到,源自hBMSCs的外泌体(hBMSC-Exos)介导细胞间通讯,并对各种肿瘤的发展表现出类似的作用。然而,hBMSC-Exos在OS发展中的作用仍不清楚,其潜在机制有待阐明。我们的结果表明,hBMSC衍生的外泌体促进OS细胞增殖、迁移和侵袭。同时,在OS细胞中沉默自噬相关基因5(ATG5)可消除hBMSC-Exos的促肿瘤作用。我们目前的研究表明,hBMSC-Exos通过促进OS中的致癌自噬来促进肿瘤发生和转移。