Acetylsalicylic acid and salicylic acid present anticancer properties against melanoma by promoting nitric oxide-dependent endoplasmic reticulum stress and apoptosis
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Nature Research
Abstract
Melanoma is the most aggressive and fatal type of skin cancer due to being highly proliferative. Acetylsalicylic acid (ASA; Aspirin) and salicylic acid (SA) are ancient drugs with multiple applications in medicine. Here, we showed that ASA and SA present anticancer effects against a murine model of implanted melanoma. These effects were also validated in 3D- and 2D-cultured melanoma B16F10 cells, where the drugs promoted pro-apoptotic effects. In both in vivo and in vitro models, SA and ASA triggered endoplasmic reticulum (ER) stress, which culminates with the upregulation of the pro-apoptotic transcription factor C/EBP homologous protein (CHOP). These effects are initiated by ASA/SA-triggered Akt/mTOR/AMPK-dependent activation of nitric oxide synthase 3 (eNOS), which increases nitric oxide and reactive oxygen species production inducing ER stress response. In the end, we propose that ASA and SA instigate anticancer effects by a novel mechanism, the activation of ER stress. © 2020, The Author(s).
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Amp-activated protein kinases, Animals, Antineoplastic agents, Apoptosis, Aspirin, Cell line, tumor, Disease models, animal, Endoplasmic reticulum stress, Male, Melanoma, Mice, inbred c57bl, Molecular targeted therapy, Nitric oxide, Nitric oxide synthase type iii, Proto-oncogene proteins c-akt, Salicylic acid, Skin neoplasms, Tor serine-threonine kinases, Up-regulation, Acetylsalicylic acid, Antineoplastic agent, Endothelial nitric oxide synthase, Hydroxymethylglutaryl coenzyme a reductase kinase, Protein kinase b, Target of rapamycin kinase, Animal, C57bl mouse, Disease model, Drug effect, Metabolism, Molecularly targeted therapy, Pathology, Skin tumor, Tumor cell line, Upregulation