Perezone and its phenyl glycine derivative induce cytotoxicity via caspases on human glial cancer cells.
M Mirian Estévez-CarmonaMaría Teresa Ramírez-ApanMontserrat Zaragoza-OjedaAnita Vega-MirandaFrancisco Arenas-HuerteroWilliam F ReynoldsMarco A Obregón-MendozaPublished in: Natural product research (2023)
The new phenyl glycine derivative of perezone was obtained in a single reaction step in ca . 80% yield which showed remarkable cytotoxic activity against the astrocytoma U-251 cell line. After 24 h of exposure, both perezone (IC 50 = 6.83 ± 1.64 µM) and its phenyl glycine derivative (2.60 ± 1.69 µM) showed cytotoxic effect on U-251 cells but were five times less cytotoxic on the non-tumoral SVGp12 cell line (IC 50 = 28.54 ± 1.59 and 31.87 ± 1.54 µM respectively). Both compounds induced cellular morphological changes (pyknosis or cytoplasmic vacuolization) and increased the expression of caspases 3, 8, and 9 genes related to apoptosis. In the acute toxicity study, phenyl glycine perezone (DL 50 = 2000 mg/Kg) demonstrated to be less toxic than perezone (DL 50 = 500 mg/Kg). Phenylglycine-perezone can envisage a beneficial therapeutic potential.
Keyphrases
- cell cycle arrest
- oxidative stress
- drug induced
- endothelial cells
- induced apoptosis
- poor prognosis
- cell death
- endoplasmic reticulum stress
- liver failure
- neuropathic pain
- genome wide
- spinal cord injury
- water soluble
- binding protein
- gene expression
- extracorporeal membrane oxygenation
- aortic dissection
- dna methylation
- spinal cord
- acute respiratory distress syndrome
- transcription factor