Molecular analyses reveal inflammatory mediators in the solid component and cyst fluid of human adamantinomatous craniopharyngioma Journal Article


Authors: Donson, A. M.; Apps, J.; Griesinger, A. M.; Amani, V.; Witt, D. A.; Anderson, R. C. E.; Niazi, T. N.; Grant, G.; Souweidane, M.; Johnston, J. M.; Jackson, E. M.; Kleinschmidt-DeMasters, B. K.; Handler, M. H.; Tan, A. C.; Gore, L.; Virasami, A.; Gonzalez-Meljem, J. M.; Jacques, T. S.; Martinez-Barbera, J. P.; Foreman, N. K.; Hankinson, T. C.; for the Advancing Treatment for Pediatric Craniopharyngioma, Consortium
Article Title: Molecular analyses reveal inflammatory mediators in the solid component and cyst fluid of human adamantinomatous craniopharyngioma
Abstract: Pediatric adamantinomatous craniopharyngioma (ACP) is a highly solid and cystic tumor, often causing substantial damage to critical neuroendocrine structures such as the hypothalamus, pituitary gland, and optic apparatus. Paracrine signaling mechanisms driving tumor behavior have been hypothesized, with IL-6R overexpression identified as a potential therapeutic target. To identify potential novel therapies, we characterized inflammatory and immunomodulatory factors in ACP cyst fluid and solid tumor components. Cytometric bead analysis revealed a highly pro-inflammatory cytokine pattern in fluid from ACP compared to fluids from another cystic pediatric brain tumor, pilocytic astrocytoma. Cytokines and chemokines with particularly elevated concentrations in ACPs were IL-6, CXCL1 (GRO), CXCL8 (IL-8) and the immunosuppressive cytokine IL-10. These data were concordant with solid tumor compartment transcriptomic data from a larger cohort of ACPs, other pediatric brain tumors and normal brain. The majority of receptors for these cytokines and chemokines were also over-expressed in ACPs. In addition to IL-10, the established immunosuppressive factor IDO-1 was overexpressed by ACPs at the mRNA and protein levels. These data indicate that ACP cyst fluids and solid tumor components are characterized by an inflammatory cytokine and chemokine expression pattern. Further study regarding selective cytokine blockade may inform novel therapeutic interventions. © 2017 American Association of Neuropathologists, Inc. All rights reserved.
Keywords: child; preschool child; child, preschool; genetics; clinical trial; metabolism; cohort studies; gene expression profiling; interleukin 6 receptor; cyst fluid; cohort analysis; pathology; physiology; gene expression regulation; gene expression regulation, neoplastic; cytokine; immunology; cytokines; messenger rna; rna, messenger; microarray analysis; multicenter study; immunomodulation; craniopharyngioma; indoleamine 2,3 dioxygenase; indoleamine-pyrrole 2,3,-dioxygenase; hypophysis tumor; il-6; pituitary neoplasms; adamantinomatous craniopharyngioma; receptors, interleukin-6; inflammatory; humans; human; male; female; craniopharyngioma cyst; indoleamine 2,3-dioxygenase 1, human
Journal Title: Journal of Neuropathology and Experimental Neurology
Volume: 76
Issue: 9
ISSN: 0022-3069
Publisher: Oxford University Press  
Date Published: 2017-09-01
Start Page: 779
End Page: 788
Language: English
DOI: 10.1093/jnen/nlx061
PUBMED: 28859336
PROVIDER: scopus
PMCID: PMC6005018
DOI/URL:
Notes: Article -- Export Date: 2 November 2017 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors