Fraxetin inhibits proliferation and induces apoptosis of bladder cancer through the Akt pathway in vitro and in vivo

Author:

Weng Mingfang1ORCID,Deng Zhen1,Huang Shuijing2,Lin Xiaowen3,Xu Na1,Sun Xinghui1,Wu Weizhen1,Lu Jun4,Wang Dong14

Affiliation:

1. Department of Urology 900TH Hospital of Joint Logistics Support Force, Fujian Medical University Fuzhou China

2. Department of Neurosurgery The First Affiliated Hospital of Fujian Medical University Fuzhou China

3. Department of Vascular Surgery Fujian Provincial People's Hospital Fuzhou China

4. Fujian Provincial Key Laboratory of Transplant Biology, Dongfang Hospital (900TH Hospital of Joint Logistics Support Force) Xiamen University Fuzhou China

Abstract

AbstractFraxetin, a natural compound extracted from the Chinese herb Cortex Fraxini, is reported to boast extensive antitumor properties in various cancers. However, whether fraxetin exhibited an anticancer effect on bladder cancer remains unknown. In this study, cell counting kit‐8 was utilized to detect cell viability. Flow cytometry analysis was performed for cell apoptosis analysis. Western blot analysis and real‐time PCR were used to ascertain gene expression analysis. A mouse bladder cancer xenograft model was established and subjected to fraxetin treatment. Fraxetin reduced the viability of bladder cancer cells, induced apoptosis in vitro, and inhibited the growth of bladder cancer in vivo. Fraxetin inhibited the Akt pathway in J82 cells. In conclusion, the growth inhibitory properties of fraxetin against bladder cancer may be mediated via an Akt inhibitory effect and cell apoptosis promotion.

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Toxicology,Molecular Biology,Molecular Medicine,Biochemistry,General Medicine

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