Components of the eIF4F complex are potential therapeutic targets for malignant peripheral nerve sheath tumors and vestibular schwannomas. Issue 9 (1st September 2016)

• Record Type: Journal Article
• Authors: Oblinger, Janet L.; Burns, Sarah S.; Akhmametyeva, Elena M.; Huang, Jie; Pan, Li; Ren, Yulin; Shen, Rulong; Miles-Markley, Beth; Moberly, Aaron C.; Kinghorn, A. Douglas; Welling, D. Bradley; Chang, Long-Sheng
• Is Part Of: Neuro-oncology. Volume 18:Issue 9(2016:Sep.)
• Page Start: 1265
• Page End: 1277
• Publication Date: 2016-09-01
• Subjects: eIF4F complex -- malignant peripheral nerve sheath tumor (MPNST) -- orthotopic mouse models -- silvestrol -- vestibular schwannoma (VS); Brain Neoplasms -- Periodicals; Brain -- Tumors -- Periodicals; Brain -- Cancer -- Periodicals; Nervous system -- Cancer -- Periodicals; 616.99481
• DOI: 10.1093/neuonc/now032
• Languages: English
• ISSNs: 1522-8517

Abstract

Abstract: Background: The eukaryotic initiation factor 4F (eIF4F) complex plays a pivotal role in protein translation initiation; however, its importance in malignant and benign Schwann cell tumors has not been explored, and whether blocking eIF4F function is effective for treating these tumors is not known. Methods: Immunostaining was performed on human malignant peripheral nerve sheath tumors (MPNSTs) and vestibular schwannomas (VSs) for eIF4F components. The role of eIF4A and eIF4E in cell growth was assessed by RNA interference. Various natural compounds were screened for their growth-inhibitory activity. Flow cytometry and Western blotting were performed to characterize the action of silvestrol, and its antitumor activity was verified in orthotopic mouse models. Results: MPNSTs and VSs frequently overexpressed eIF4A, eIF4E, and/or eIF4G. Depletion of eIF4A1, eIF4A2, and eIF4E substantially reduced MPNST cell growth. From screening a panel of plant-derived compounds, the eIF4A inhibitor silvestrol was identified as a leading agent with nanomolar IC50 values in MPNST and VS cells. Silvestrol induced G2 /M arrest in both NF1 -deficient and NF1 -expressing MPNST cells and primary VS cells. Silvestrol consistently decreased the levels of multiple cyclins, Aurora A, and mitogenic kinases AKT and ERKs. Silvestrol treatment dramatically suppressed tumor growth in mouse models for NF1 −/− MPNST and Nf2 −/− schwannoma. This decreased tumor growth was accompanied by elevated phospho-histone H3 and TUNEL labeling, consistent with G2 /M arrest and apoptosis in silvestrol-treated tumor cells. Conclusions: The eIF4F complex is a potential therapeutic target in MPNSTs and VS, and silvestrol may be a promising agent for treating these tumors.