A novel Diels–Alder adduct of mulberry leaves exerts anticancer effect through autophagy-mediated cell death

被引:0
|
作者
Yu-han Shu
Hua-hua Yuan
Meng-ting Xu
Ye-ting Hong
Cheng-cheng Gao
Zhi-pan Wu
Hao-te Han
Xin Sun
Rui-lan Gao
Si-fu Yang
Shou-xin Li
Jing-kui Tian
Jian-bin Zhang
机构
[1] College of Biomedical Engineering and Instrument Science,Department of Oncology
[2] Zhejiang University,Department of Hematology
[3] Clinical Research Institute,undefined
[4] Zhejiang Provincial People’s Hospital,undefined
[5] People’s Hospital of Hangzhou Medical College,undefined
[6] Hangzhou Medical College,undefined
[7] Zhejiang Provincial People’s Hospital,undefined
[8] People’s Hospital of Hangzhou Medical College,undefined
[9] The First Affiliated Hospital of Zhejiang Chinese Medical University,undefined
[10] Key Laboratory for Biomedical Engineering of Ministry of Education,undefined
[11] Zhejiang-Malaysia Joint Research Center for Traditional Medicine,undefined
[12] Zhejiang University,undefined
来源
Acta Pharmacologica Sinica | 2021年 / 42卷
关键词
Guangsangon E; autophagy; ER stress; respiratory cancer;
D O I
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中图分类号
学科分类号
摘要
Guangsangon E (GSE) is a novel Diels–Alder adduct isolated from leaves of Morus alba L, a traditional Chinese medicine widely applied in respiratory diseases. It is reported that GSE has cytotoxic effect on cancer cells. In our research, we investigated its anticancer effect on respiratory cancer and revealed that GSE induces autophagy and apoptosis in lung and nasopharyngeal cancer cells. We first observed that GSE inhibits cell proliferation and induces apoptosis in A549 and CNE1 cells. Meanwhile, the upregulation of autophagosome marker LC3 and increased formation of GFP–LC3 puncta demonstrates the induction of autophagy in GSE-treated cells. Moreover, GSE increases the autophagy flux by enhancing lysosomal activity and the fusion of autophagosomes and lysosomes. Next, we investigated that endoplasmic reticulum (ER) stress is involved in autophagy induction by GSE. GSE activates the ER stress through reactive oxygen species (ROS) accumulation, which can be blocked by ROS scavenger NAC. Finally, inhibition of autophagy attenuates GSE-caused cell death, termed as “autophagy-mediated cell death.” Taken together, we revealed the molecular mechanism of GSE against respiratory cancer, which demonstrates great potential of GSE in the treatment of representative cancer.
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页码:780 / 790
页数:10
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