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Home > Literature List > Narciclasine induces autophagy‐dependent apoptosis in triple‐negative breast cancer cells by regulating the AMPK‐ULK1 axis

Narciclasine induces autophagy‐dependent apoptosis in triple‐negative breast cancer cells by regulating the AMPK‐ULK1 axis

Journal name: Cell Proliferation
Literature No.:
Literature Url: https://doi.org/10.1111/cpr.12518
Date publication:28 August 2018
Objectives

Autophagy and apoptosis are major types of eukaryotic programmed cell death, and regulating these processes holds promise for treating cancers. In this study, we explored the regulation mechanisms of narciclasine to autophagy and apoptosis processes in triple‐negative breast cancer.

Materials and Methods

Effects of narciclasine on proliferation, apoptosis, and autophagy of HCC‐1937 and MDA‐MB‐231 triple‐negative breast cancer (TNBC) cells were assessed using transmission electronic microscopy, flow cytometry following staining with Annexin V‐FITC and propidium iodide, RNA sequencing, real‐time PCR, and Western blotting. The ability of narciclasine to inhibit growth of human HCC1937 TNBC xenografts in mice was assessed, and potential mechanisms of inhibition were explored using immunohistochemistry.

Results

Narciclasine inhibited TNBC cell proliferation and induced autophagy‐dependent apoptosis in a dose‐dependent manner. These apoptotic effects could be reversed using autophagy inhibitors, including an AMPK inhibitor and ULK1 siRNA. Consistent with these in vitro results, narciclasine significantly inhibited TNBC tumour growth in mice by upregulating autophagy‐dependent apoptosis.

Conclusions

Our findings suggest that narciclasine regulates the AMPK‐ULK1 signalling axis to promote autophagy‐dependent apoptosis, demonstrating therapeutic potential against TNBC.

… 2 | MATERIALS AND METHODS 2.1 | Chemicals and reagents Narciclasine was purchased from Biopurify Phytochemical (Chengdu, China), dissolved in dimethyl sulphoxide (DMSO) to make stock solutions, and diluted to final concentrations in culture medium …  
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