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Xanthatin inhibits STAT3 and NF-?B signalling by covalently binding to JAK and IKK kinases.


ABSTRACT: Aberrant activation of the signal transducer and activator of transcription 3 (STAT3) and the nuclear factor-?B (NF-?B) signalling pathways is associated with the development of cancer and inflammatory diseases. JAKs and IKKs are the key regulators in the STAT3 and NF-?B signalling respectively. Therefore, the two families of kinases have been the major targets for developing drugs to regulate the two signalling pathways. Here, we report a natural compound xanthatin from the traditional Chinese medicinal herb Xanthium L. as a potent inhibitor of both STAT3 and NF-?B signalling pathways. Our data demonstrated that xanthatin was a covalent inhibitor and its activities depended on its ?-methylene-?-butyrolactone group. It preferentially interacted with the Cys243 of JAK2 and the Cys412 and Cys464 of IKK? to inactivate their activities. In doing so, xanthatin preferentially inhibited the growth of cancer cell lines that have constitutively activated STAT3 and p65. These data suggest that xanthatin may be a promising anticancer and anti-inflammation drug candidate.

SUBMITTER: Liu M 

PROVIDER: S-EPMC6533482 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

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Xanthatin inhibits STAT3 and NF-κB signalling by covalently binding to JAK and IKK kinases.

Liu Man M   Xiao Cheng-Qian CQ   Sun Ming-Wei MW   Tan Min-Jia MJ   Hu Li-Hong LH   Yu Qiang Q  

Journal of cellular and molecular medicine 20190416 6


Aberrant activation of the signal transducer and activator of transcription 3 (STAT3) and the nuclear factor-κB (NF-κB) signalling pathways is associated with the development of cancer and inflammatory diseases. JAKs and IKKs are the key regulators in the STAT3 and NF-κB signalling respectively. Therefore, the two families of kinases have been the major targets for developing drugs to regulate the two signalling pathways. Here, we report a natural compound xanthatin from the traditional Chinese  ...[more]

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