Aspirin activates resolution pathways to reprogram T cell and macrophage responses in colitis-associated colorectal cancer

Autor: Roberta De Matteis, Magdalena B. Flak, Maria Gonzalez-Nunez, Shani Austin-Williams, Francesco Palmas, Romain A. Colas, Jesmond Dalli
Jazyk: angličtina
Rok vydání: 2022
Předmět:
Zdroj: De Matteis, R, Flak, M B, Gonzales-Nunez, M, Austin-Williams, S, Palmas, F, Colas, R A & Dalli, J 2022, ' Aspirin activates resolution pathways to reprogram T cell and macrophage responses in colitis-associated colorectal cancer ', Science Advances, vol. 8, no. 5, eabl5420 . https://doi.org/10.1126/sciadv.abl5420
DOI: 10.1126/sciadv.abl5420
Popis: Inflammation is linked with carcinogenesis in many types of cancer including colorectal cancer (CRC). Aspirin is recommended for the prevention of CRC, although the mechanism(s) mediating its immunomodulatory actions remain incompletely understood. Here, we demonstrate that aspirin increased concentrations of the immune-regulatory aspirin-triggered specialized proresolving mediators (AT-SPMs), including AT-lipoxin A 4 and AT-resolvin D1, in colonic tissues during inflammation-associated CRC (I-CRC). Aspirin also down-regulated the expression of the checkpoint protein programmed cell death protein-1 in macrophages and CD8 + T cells from the colonic mucosa. Inhibition of AT-SPM biosynthesis or knockout of the AT-SPM receptor Alx/Fpr2 reversed the immunomodulatory actions of aspirin on macrophages and CD8 + T cells and abrogated its protective effects during I-CRC. Furthermore, treatment of mice with AT-SPM recapitulated the immune-directed actions of aspirin during I-CRC. Together, these findings elucidate a central role for AT-SPM in mediating the immune-directed actions of aspirin in regulating I-CRC progression.
Databáze: OpenAIRE