Cargando…

Enteric Glia Play a Critical Role in Promoting the Development of Colorectal Cancer

Enteric glia are a distinct population of peripheral glial cells in the enteric nervous system that regulate intestinal homeostasis, epithelial barrier integrity, and gut defense. Given these unique attributes, we investigated the impact of enteric glia depletion on tumor development in azoxymethane...

Descripción completa

Detalles Bibliográficos
Autores principales: Yuan, Robert, Bhattacharya, Nupur, Kenkel, Justin A., Shen, Jeanne, DiMaio, Michael A., Bagchi, Sreya, Prestwood, Tyler R., Habtezion, Aida, Engleman, Edgar G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691584/
https://www.ncbi.nlm.nih.gov/pubmed/33282743
http://dx.doi.org/10.3389/fonc.2020.595892
Descripción
Sumario:Enteric glia are a distinct population of peripheral glial cells in the enteric nervous system that regulate intestinal homeostasis, epithelial barrier integrity, and gut defense. Given these unique attributes, we investigated the impact of enteric glia depletion on tumor development in azoxymethane/dextran sodium sulfate (AOM/DSS)-treated mice, a classical model of colorectal cancer (CRC). Depleting GFAP(+) enteric glia resulted in a profoundly reduced tumor burden in AOM/DSS mice and additionally reduced adenomas in the Apc(Min)(/+) mouse model of familial adenomatous polyposis, suggesting a tumor-promoting role for these cells at an early premalignant stage. This was confirmed in further studies of AOM/DSS mice, as enteric glia depletion did not affect the properties of established malignant tumors but did result in a marked reduction in the development of precancerous dysplastic lesions. Surprisingly, the protective effect of enteric glia depletion was not dependent on modulation of anti-tumor immunity or intestinal inflammation. These findings reveal that GFAP(+) enteric glia play a critical pro-tumorigenic role during early CRC development and identify these cells as a potential target for CRC prevention.