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Cell Death Differ ; 21(12): 1914-24, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25124554

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, LXRß 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 LXRß, pannexin 1, NLRP3 and caspase-1 within the tumor cells. Our results demonstrate that LXRß, through pannexin 1 interaction, can specifically induce caspase-1-dependent colon cancer cell death by pyroptosis.


Subject(s)
Apoptosis , Orphan Nuclear Receptors/metabolism , Adenosine Triphosphate/metabolism , Animals , Antineoplastic Agents/pharmacology , Carrier Proteins/metabolism , Caspase 1/metabolism , Colonic Neoplasms/drug therapy , Colonic Neoplasms/metabolism , Connexins/metabolism , Drug Screening Assays, Antitumor , Female , HCT116 Cells , HEK293 Cells , HT29 Cells , Humans , Hydrocarbons, Fluorinated/pharmacology , Liver X Receptors , Mice, Inbred BALB C , NLR Family, Pyrin Domain-Containing 3 Protein , Neoplasm Transplantation , Nerve Tissue Proteins/metabolism , Orphan Nuclear Receptors/agonists , Sulfonamides/pharmacology , Tumor Burden/drug effects
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