Key Laboratory of Stem Cells and Regenerative Medicine, Institute of Molecular and Clinical Medicine, Kunming Medical University, Kunming, Yunnan, P.R. China.
Oncol Rep. 2013 Dec;30(6):2719-24. doi: 10.3892/or.2013.2746. Epub 2013 Sep 20.
High-grade glioma is incurable and is associated with a short survival time and a poor prognosis. There are two forms of brain-derived neurotrophic factor (BDNF), proBDNF and mature BDNF, which exert opposite effects. Their diverse actions are mediated through two different transmembrane receptor signalling systems: p75NTR and TrkB. The important roles of the BDNF/TrkB signalling system in tumour cell proliferation and survival have been demonstrated. However, few studies have been able to distinguish mature BDNF from proBDNF due to the limitation of specific antibodies. Using specific proBDNF antibodies, we demonstrated that the proBDNF/p75NTR pathway appears to inhibit malignant glioma cell growth and migration. In the present study using specific mature BDNF antibodies, we found that mature BDNF inhibited C6 glioma cell apoptosis and increased cell growth and migration in vitro. Our data suggest that the counterbalance between mature BDNF and proBDNF may regulate tumour growth.
高级别神经胶质瘤是无法治愈的,患者生存时间短,预后差。脑源性神经营养因子 (BDNF) 有两种形式,即前体 BDNF 和成熟 BDNF,它们发挥着相反的作用。它们的不同作用是通过两种不同的跨膜受体信号系统介导的:p75NTR 和 TrkB。BDNF/TrkB 信号系统在肿瘤细胞增殖和存活中的重要作用已经得到证实。然而,由于特异性抗体的限制,很少有研究能够区分成熟 BDNF 和前体 BDNF。使用特异性前体 BDNF 抗体,我们证明前体 BDNF/p75NTR 途径似乎可以抑制恶性神经胶质瘤细胞的生长和迁移。在本研究中,使用特异性成熟 BDNF 抗体,我们发现成熟 BDNF 抑制 C6 神经胶质瘤细胞凋亡,并增加体外细胞生长和迁移。我们的数据表明,成熟 BDNF 和前体 BDNF 之间的平衡可能调节肿瘤生长。