Dorandish Sadaf, Atali Sarah, Ray Ravel, Al Khashali Hind, Coleman Kai-Ling, Guthrie Jeffrey, Heyl Deborah, Evans Hedeel Guy
Chemistry Department, Eastern Michigan University, Ypsilanti, MI 48197, USA.
Int J Mol Sci. 2021 Jun 30;22(13):7059. doi: 10.3390/ijms22137059.
Brain-derived neurotrophic factor (BDNF), a member of the neurotrophin family, has been linked to several human malignancies and shown to promote tumorigenesis. The purpose of this study was to explore the relative abundance of pro-brain-derived neurotrophic factor (proBDNF) and mature BDNF (mBDNF) in A549 (p53 wild-type) and H1299 (p53-null) lung cancer cell media. Higher levels of proBDNF were detected in the media of A549 cells than in H1299 cell media. Using inhibitors, we found that the levels of proBDNF and mBDNF in the media are likely regulated by PI3K, AKT, and NFκB. However, the largest change in these levels resulted from MMP2/9 inhibition. Blocking p53 function in A549 cells resulted in increased mBDNF and decreased proBDNF, suggesting a role for p53 in regulating these levels. The ratio of proBDNF/mBDNF was not affected by MMP2 knockdown but increased in the media of both cell lines upon knockdown of MMP9. Downregulation of either MMP2 or MMP9 by siRNA showed that MMP9 siRNA treatment of either A549 or H1299 cells resulted in decreased cell viability and increased apoptosis, an effect diminished upon the same treatment with proBDNF immunodepleted media, suggesting that MMP9 regulates the cytotoxic effects induced by proBDNF in lung cancer cells.
脑源性神经营养因子(BDNF)是神经营养因子家族的一员,与多种人类恶性肿瘤相关,并已证明可促进肿瘤发生。本研究的目的是探讨A549(p53野生型)和H1299(p53缺失型)肺癌细胞培养基中前脑源性神经营养因子(proBDNF)和成熟BDNF(mBDNF)的相对丰度。在A549细胞培养基中检测到的proBDNF水平高于H1299细胞培养基。使用抑制剂,我们发现培养基中proBDNF和mBDNF的水平可能受PI3K、AKT和NFκB调节。然而,这些水平的最大变化是由MMP2/9抑制引起的。在A549细胞中阻断p53功能导致mBDNF增加和proBDNF减少,表明p53在调节这些水平中起作用。proBDNF/mBDNF的比值不受MMP2敲低的影响,但在两种细胞系的培养基中,MMP9敲低后该比值增加。通过siRNA下调MMP2或MMP9表明,用MMP9 siRNA处理A549或H1299细胞会导致细胞活力降低和凋亡增加,在用proBDNF免疫耗尽的培养基进行相同处理后,这种效应减弱,表明MMP9调节proBDNF在肺癌细胞中诱导的细胞毒性作用。