Ethanol extract of Vanilla planifolia stems reduces PAK6 expression and induces cell death in glioblastoma cells.
Hui Hua ChangAlice Y W ChangBing-Chen TsaiYu-Ju ChenSung-Ghun WuLi-Jyun ChenYi-Xuan LinYuan-Shuo HsuehPublished in: Journal of cellular and molecular medicine (2024)
Glioblastoma multiforme (GBM) is a malignant tumour with a poor prognosis. Therefore, potential treatment strategies and novel therapeutic targets have gained increased attention. Our data showed that the ethanol extract of Vanilla planifolia stem (VAS) significantly decreased the viability and the colony formation of GBM cells. Moreover, VAS induced the cleavage of MAP1LC3, a marker of autophagy. Further RNA-seq and bioinformatic analysis revealed 4248 differentially expressed genes (DEGs) between VAS-treated GBM cells and the control cells. Protein-protein interactions between DEGs with fold changes less than -3 and more than 5 were further analysed, and we found that 16 and 9 hub DEGs, respectively, were correlated with other DEGs. Further qPCR experiments confirmed that 14 hub DEGs was significantly downregulated and 9 hub DEGs was significantly upregulated. In addition, another significantly downregulated DEG, p21-activated kinase 6 (PAK6), was correlated with the overall survival of GBM patients. Further validation experiments confirmed that VAS significantly reduced the mRNA and protein expression of PAK6, which led to the abolition of cell viability and colony formation. These findings demonstrated that VAS reduced cell viability, suppressed colony formation and induced autophagy and revealed PAK6 and other DEGs as potential therapeutic targets for GBM treatment.
Keyphrases
- induced apoptosis
- cell death
- cell cycle arrest
- poor prognosis
- rna seq
- endoplasmic reticulum stress
- oxidative stress
- single cell
- signaling pathway
- long non coding rna
- newly diagnosed
- genome wide
- machine learning
- diabetic rats
- end stage renal disease
- network analysis
- cell proliferation
- climate change
- high resolution
- risk assessment
- mass spectrometry
- peritoneal dialysis
- tyrosine kinase
- dna binding
- protein kinase
- tandem mass spectrometry
- solid phase extraction