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Contributions of inflammation and tumor microenvironment to neurofibroma tumorigenesis.

Contributions of inflammation and tumor microenvironment to neurofibroma tumorigenesis.
Author Information (click to view)

Liao CP, C Booker R, Brosseau JP, Chen Z, Mo J, Tchegnon E, Wang Y, Wade Clapp D, Q Le L,


Liao CP, C Booker R, Brosseau JP, Chen Z, Mo J, Tchegnon E, Wang Y, Wade Clapp D, Q Le L, (click to view)

Liao CP, C Booker R, Brosseau JP, Chen Z, Mo J, Tchegnon E, Wang Y, Wade Clapp D, Q Le L,

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The Journal of clinical investigation 2018 03 29() doi 10.1172/JCI99424

Abstract

Neurofibromatosis type 1 associates with multiple neoplasms and the Schwann cell tumor neurofibroma is the most prevalent. A hallmark feature of neurofibroma is mast cell infiltration which is recruited by chemoattractant stem cell factor (SCF) that has been suggested to sustain neurofibroma tumorigenesis. In this study, using new genetically engineered Scf mice, we decipher the contributions of tumor-derived SCF and mast cells to neurofibroma development. We demonstrate that mast cell infiltration is dependent on SCF from tumor Schwann cells. However, removal of mast cells by depleting this main SCF source only slightly affects neurofibroma progression. Other inflammation signatures show that all neurofibromas are associated with high levels of macrophages regardless of Scf status. These findings suggest an active inflammation in neurofibromas and partly explain why mast cell removal alone is not sufficient to relieve tumor burden in this experimental neurofibroma model. Furthermore, we show that plexiform neurofibromas are highly associated with injury-prone spinal nerves that are close to flexible vertebras. In summary, our study details the role of inflammation in neurofibromagenesis. These data paired with the observed tumor locations indicate that prevention of inflammation, and possibly nerve injury, are therapeutic approaches for neurofibroma prophylaxis and treatment that should be explored.

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