[HTML][HTML] Liver X receptor β activation induces pyroptosis of human and murine colon cancer cells

V Derangere, A Chevriaux, F Courtaut… - Cell Death & …, 2014 - nature.com
V Derangere, A Chevriaux, F Courtaut, M Bruchard, H Berger, F Chalmin, SZ Causse…
Cell Death & Differentiation, 2014nature.com
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 …
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.
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