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


ABSTRACT: 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 invitro 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.

SUBMITTER: Zhao Y 

PROVIDER: S-EPMC5739552 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

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

Zhao Yue Y   Guo Qinglong Q   Zhao Kai K   Zhou Yuxin Y   Li Wenjun W   Pan Chuyue C   Qiang Lei L   Li Zhiyu Z   Lu Na N  

Oncoimmunology 20170921 1


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 <i>in</i><i>vitro</i> and <i>in vivo</i>, which trigger autophagy to degraded NLRP3 inflammasome. Treatment with  ...[more]

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