| Literature DB >> 25124554 |
V Derangère1, A Chevriaux2, F Courtaut3, M Bruchard3, H Berger3, F Chalmin3, S Z Causse4, E Limagne3, F Végran3, S Ladoire1, B Simon5, W Boireau5, A Hichami3, L Apetoh1, G Mignot4, F Ghiringhelli1, C Rébé2.
Abstract
Liver X receptors (LXRs) have been proposed to have some anticancer properties, through molecular mechanisms that remain elusive. Here we report for the first time that LXR ligands induce caspase-1-dependent cell death of colon cancer cells. Caspase-1 activation requires Nod-like-receptor pyrin domain containing 3 (NLRP3) inflammasome and ATP-mediated P2 × 7 receptor activation. Surprisingly, LXRβ is mainly located in the cytoplasm and has a non-genomic role by interacting with pannexin 1 leading to ATP secretion. Finally, LXR ligands have an antitumoral effect in a mouse colon cancer model, dependent on the presence of LXRβ, pannexin 1, NLRP3 and caspase-1 within the tumor cells. Our results demonstrate that LXRβ, through pannexin 1 interaction, can specifically induce caspase-1-dependent colon cancer cell death by pyroptosis.Entities:
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Year: 2014 PMID: 25124554 PMCID: PMC4227150 DOI: 10.1038/cdd.2014.117
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 15.828