Small molecule GL-V9 protects against colitis-associated colorectal cancer by limiting NLRP3 inflammasome through autophagy

Emerging evidence suggests that NLRP3 inflammasome provides a link between colitis-associated colorectal cancer and inflammatory bowel diseases. Autophagy is induced in macrophages by AMPK activation and regulates NLRP3 inflammasome to maintain intracellular homeostasis. Here we report that a small-...

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Veröffentlicht in:Oncoimmunology 2018-01, Vol.7 (1), p.e1375640
Hauptverfasser: Zhao, Yue, Guo, Qinglong, Zhao, Kai, Zhou, Yuxin, Li, Wenjun, Pan, Chuyue, Qiang, Lei, Li, Zhiyu, Lu, Na
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Sprache:eng
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Zusammenfassung:Emerging evidence suggests that NLRP3 inflammasome provides a link between colitis-associated colorectal cancer and inflammatory bowel diseases. Autophagy is induced in macrophages by AMPK activation and regulates NLRP3 inflammasome to maintain intracellular homeostasis. Here we report that a small-molecule AMPK activator (GL-V9) exerts potent anti-inflammatory effects on macrophages in vitro and in vivo, which trigger autophagy to degraded NLRP3 inflammasome. Treatment with GL-V9 protected against colitis and tumorigenesis in colitis-associated colorectal cancer. This suggests that GL-V9 may be an interesting candidate for clinical evaluation in the treatment of colitis-associated colorectal cancer.
ISSN:2162-4011
2162-402X
2162-402X
DOI:10.1080/2162402X.2017.1375640