Synthesis and biological evaluation of matrine derivatives containing benzo-α-pyrone structure as potent anti-lung cancer agents

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作者
Lichuan Wu
Guizhen Wang
Shuaibing Liu
Jinrui Wei
Sen Zhang
Ming Li
Guangbiao Zhou
Lisheng Wang
机构
[1] School of Chemistry and Chemical Engineering,
[2] Guangxi University,undefined
[3] State Key Laboratory of Membrane Biology,undefined
[4] Institute of Zoology,undefined
[5] Chinese Academy of Sciences,undefined
[6] Guangxi Scientific Research Center of Traditional Chinese Medicine,undefined
[7] Guangxi University of Chinese Medicine,undefined
[8] Key Laboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Sciences and Yunnan Province,undefined
[9] Kunming Institute of Zoology,undefined
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摘要
Matrine, an active component of root extracts from Sophora flavescens Ait, is the main chemical ingredient of Fufang Kushen injection which was approved by Chinese FDA (CFDA) in 1995 as an anticancer drug to treat non-small cell lung cancer and liver cancer in combination with other anticancer drugs. Owning to its druggable potential, matrine is considered as an ideal lead compound for modification. We delineate herein the synthesis and anticancer effects of 17 matrine derivatives bearing benzo-α-pyrone structures. The results of cell viability assays indicated that most of the target compounds showed improved anticancer effects. Further studies showed that compound 5i could potently inhibit lung cancer cell proliferation in vitro and in vivo with no obvious side effects. Moreover, compound 5i could induce G1 cell cycle arrest and autophagy in lung cancer cells through up-regulating P27, down-regulating CDK4 and cyclinD1 and attenuating PI3K/Akt/mTOR pathway. Suppression of autophagy attenuated 5i induced proliferation inhibition. Collectively, our results infer that matrine derivative 5i bears therapeutic potentials for lung cancer.
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