Electrochemotherapy with Mitomycin C Potentiates Apoptosis Death by Inhibiting Autophagy in Squamous Carcinoma Cells.
Maria CondelloGloria D'AvackRosa VonaEnrico Pierluigi SpugniniLicia ScaccoStefania MeschiniPublished in: Cancers (2021)
We investigated the chemosensitizing effect of electroporation (EP), which, using electrical pulses, permeabilizes cancer cells to drugs. The study involved two human hypopharyngeal and tongue carcinoma cell lines. The surface and intracytoplasmic expression of P-gp were evaluated by flow cytometry, demonstrating that both lines were intrinsically resistant. After establishing the optimal dose of mitomycin C (MMC) to be used, in combination with EP, we showed, by both MTT assay and optical and electron scanning microscopy, the potentiating cytotoxic effect of EP with MMC compared to single treatments. Flow cytometry showed that the cytotoxicity of EP + MMC was due to the induction of apoptosis. In addition to verifying the release of cytochrome C in EP + MMC samples, we performed an expression analysis of caspase-3, caspase-9, Akt, pAkt, HMGB1, LC3I, LC3II, p62, Beclin1, and associated proteins with both apoptotic and autophagic phenomena. Our results were confirmed by two veterinary patients in whom the EP + MMC combination was used to control margins after the resection of corneal squamous carcinoma. In conclusion, we affirmed that the effect for which EP enhances MMC treatment is due to the inhibition of the autophagic process induced by the drug in favor of apoptosis.
Keyphrases
- cell death
- flow cytometry
- cell cycle arrest
- endoplasmic reticulum stress
- oxidative stress
- poor prognosis
- high resolution
- signaling pathway
- induced apoptosis
- end stage renal disease
- high grade
- endothelial cells
- chronic kidney disease
- low grade
- high throughput
- emergency department
- newly diagnosed
- simultaneous determination
- optical coherence tomography
- ejection fraction
- binding protein
- combination therapy
- peritoneal dialysis
- adverse drug
- pi k akt
- liquid chromatography
- atomic force microscopy
- electron transfer
- single cell