Mechanistic Insights about Sorafenib-, Valproic Acid- and Metformin-Induced Cell Death in Hepatocellular Carcinoma.
Edgar Xchel Franco-JuárezVianey González-VillasanaMaría Elena Camacho-MollLuisa Rendón-GarlantPatricia Nefertari Ramírez-FloresBeatriz Silva-RamírezKatia Peñuelas-UrquidesEthel Daniela Cabello-RuizFabiola Castorena-TorresMario Bermudez de LeonPublished in: International journal of molecular sciences (2024)
Hepatocellular carcinoma (HCC) is among the main causes of death by cancer worldwide, representing about 80-90% of all liver cancers. Treatments available for advanced HCC include atezolizumab, bevacizumab, sorafenib, among others. Atezolizumab and bevacizumab are immunological options recently incorporated into first-line treatments, along with sorafenib, for which great treatment achievements have been reached. However, sorafenib resistance is developed in most patients, and therapeutical combinations targeting cancer hallmark mechanisms and intracellular signaling have been proposed. In this review, we compiled evidence of the mechanisms of cell death caused by sorafenib administered alone or in combination with valproic acid and metformin and discussed them from a molecular perspective.
Keyphrases
- cell death
- papillary thyroid
- end stage renal disease
- squamous cell
- chronic kidney disease
- newly diagnosed
- ejection fraction
- prognostic factors
- cell cycle arrest
- squamous cell carcinoma
- childhood cancer
- oxidative stress
- peritoneal dialysis
- lymph node metastasis
- metastatic colorectal cancer
- high glucose
- drug delivery
- cancer therapy
- diabetic rats
- drug induced
- endothelial cells
- reactive oxygen species