Merlin/NF2 regulates angiogenesis in schwannomas through a Rac1/semaphorin 3F-dependent mechanism.

Abstract

Neurofibromatosis type 2 (NF2) is an autosomal-dominant multiple neoplasia syndrome that results from mutations in the NF2 tumor suppressor gene. Patients with NF2 develop hallmark schwannomas that require surgery or radiation, both of which have significant adverse effects. Recent studies have indicated that the tumor microenvironment-in particular, tumor blood vessels-of schwannomas may be an important therapeutic target. Furthermore, although much has been done to understand how merlin, the NF2 gene product, functions as a tumor suppressor gene in schwannoma cells, the functional role of merlin in the tumor microenvironment and the mechanism(s) by which merlin regulates angiogenesis to support schwannoma growth is largely unexplored. Here we report that the expression of semaphorin 3F (SEMA3F) was specifically downregulated in schwannoma cells lacking merlin/NF2. When we reintroduced SEMA3F in schwannoma cells, we observed normalized tumor blood vessels, reduced tumor burden, and extended survival in nude mice bearing merlin-deficient brain tumors. Next, using chemical inhibitors and gene knockdown with RNA interference, we found that merlin regulated expression of SEMA3F through Rho GTPase family member Rac1. This study shows that, in addition to the tumor-suppressing activity of merlin, it also functions to maintain physiological angiogenesis in the nervous system by regulating antiangiogenic factors such as SEMA3F. Restoring the relative balance of proangiogenic and antiangiogenic factors, such as increases in SEMA3F, in schwannoma microenvironment may represent a novel strategy to alleviate the clinical symptoms of NF2-related schwannomas.

• Authors: Hon-Kit Wong, Akio Shimizu, Nathaniel D Kirkpatrick, Igor Garkavtsev, Annie W Chan, Emmanuelle di Tomaso, Michael Klagsbrun, Rakesh K Jain
• Journal: Neoplasia (New York, N.Y.) (Neoplasia) Vol. 14 Issue 2 Pg. 84-94 (Feb 2012) ISSN: 1476-5586 [Electronic] United States
• PMID: 22431917 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Membrane Proteins
• Nerve Tissue Proteins
• Neurofibromin 2
• RAC1 protein, human
• SEMA3F protein, human
• Thrombospondins
• thrombospondin 2
• rac1 GTP-Binding Protein

Topics

• Animals
• Blood Vessels (metabolism)
• Brain Neoplasms (blood supply, metabolism, pathology)
• Cell Line, Tumor
• Down-Regulation
• Gene Expression Profiling
• Gene Expression Regulation, Neoplastic
• Human Umbilical Vein Endothelial Cells
• Humans
• Kaplan-Meier Estimate
• Membrane Proteins (genetics, metabolism)
• Mice
• Mice, Nude
• Neoplasm Transplantation
• Neovascularization, Pathologic
• Nerve Tissue Proteins (genetics, metabolism)
• Neurilemmoma (blood supply, metabolism, pathology)
• Neurofibromatosis 2 (metabolism, pathology)
• Neurofibromin 2 (genetics, metabolism)
• Permeability
• Signal Transduction
• Thrombospondins (genetics, metabolism)
• rac1 GTP-Binding Protein (metabolism)