NLRP3 inflammasome in fibroblasts links tissue damage with inflammation in breast cancer progression and metastasis
Menée in vitro et à l'aide de modèles murins de cancer mammaire, cette étude met en évidence un mécanisme par lequel les fibroblastes associés au cancer, en détectant les motifs moléculaires associés aux dégâts tissulaires, activent NLPR3, une protéine impliquée dans le processus inflammatoire, et favorisent la progression tumorale ainsi que le développement de métastases
Cancer-Associated Fibroblasts (CAFs) were shown to orchestrate tumour-promoting inflammation in multiple malignancies, including breast cancer. However, the molecular pathways that govern the inflammatory role of CAFs are poorly characterised. In this study we found that fibroblasts sense damage-associated molecular patterns (DAMPs), and in response activate the NLRP3 inflammasome pathway, resulting in instigation of pro-inflammatory signalling and secretion of IL-1β. This upregulation was evident in CAFs in mouse and in human breast carcinomas. Moreover, CAF-derived inflammasome signalling facilitated tumour growth and metastasis, which was attenuated when NLRP3 or IL-1β were specifically ablated. Functionally, CAF-derived inflammasome promoted tumour progression and metastasis by modulating the tumour microenvironment towards an immune suppressive milieu and by upregulating the expression of adhesion molecules on endothelial cells. Our findings elucidate a mechanism by which CAFs promote breast cancer progression and metastasis, by linking the physiological tissue damage response of fibroblasts with tumour-promoting inflammation.