Title:Aesculetin Inhibits Proliferation and Induces Mitochondrial Apoptosis in Bladder
Cancer Cells by Suppressing the MEK/ERK Signaling Pathway
Volume: 23
Issue: 4
Author(s): Li Han, Peiwu Li, Xu Fu, Zhenzhen Huang and Wen Yin*
Affiliation:
- Department of Pharmacy, Lanzhou
University Second Hospital, Lanzhou, China
Keywords:
Bladder cancer, aesculetin, MEK/ERK, proliferation, apoptosis, migration and invasion.
Abstract:
Background: Aesculetin (AE), a natural coumarin derivative found in traditional medicinal herbs, has a
variety of pharmacological effects. However, the role of AE and its molecular mechanisms of action on bladder cancer
remains undefined.
Objective: The study aims to explore the anti-tumor effects of AE on bladder cancer cells and the associated molecular
mechanisms.
Methods: We performed a Cell Counting Kit-8 assay to examine the inhibitory effects of AE on 5637 and T24 cells.
The anti-tumor effects of AE on 5637 cells were evaluated by performing colony formation, living/dead cell staining,
apoptosis, cell cycle, migration and invasion assays. The expression levels of related proteins were determined using
western blotting.
Results: The viability of 5637 and T24 cells was decreased by AE. AE significantly inhibited colony formation, arrested
the cell cycle at the G0/G1 phase, decreased migration and invasion, decreased the mitochondrial membrane potential
and increased apoptosis in 5637 cells. Western blotting results showed the release of cytochrome C from mitochondria;
the activation of caspase-9 and caspase-3; decrease in CDK4, CCND1, MMP2 and MMP9 levels and an
increase in the BAX/BCL-2 protein ratio after treatment with AE. AE also downregulated the levels of p-ERK and p-
MEK proteins. Pre-treatment with U0126 significantly enhanced the anti-tumor effects of AE.
Conclusions: AE inhibited the proliferation and induced the apoptosis of bladder cancer cells through the MEK/ERK
pathway. These findings provide possible therapeutic strategies for bladder cancer.