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Palabras clave – provistas por la editorial

cell adhesion; plasma medicine; oncology; cold atmospheric plasma; selectivity; plasma-treated liquid; dielectric barrier discharge; pancreatic cancer; pancreatic stellate cells; immunogenic cell death; dendritic cells; cell communication; extracellular matrix (ECM); reactive oxygen and nitrogen species (ROS); tumour microenvironment (TME); extracellular vesicles; communication junctions; three-dimensional in vitro culture models; apoptosis; breast cancer; genome-wide expression; reactive oxygen species; anticancer drugs; screening; tumor spheroids; combination therapy; kINPen; reactive oxygen and nitrogen species; ROS; cancer; non-thermal atmospheric pressure plasma (NTP); indirect treatment; plasma-treated phosphate-buffered saline; electroporation; electric pulses; pulsed electric field amplitude; melanoma; long-lived reactive species; bone cancer; osteosarcoma; reactive species; plasma-activated liquid; Ringer’s saline; organotypic model; nonthermal biocompatible plasma; soft jet plasma; human glioblastoma; p38/MAPK pathway; tissue penetration; non-thermal plasma; non-invasive plasma treatment (NIPP); cervical intraepithelial neoplasia (CIN); Raman imaging; Raman microspectroscopy; Plasma lipid interactions; cold physical plasma; radiation therapy; radio-frequency discharge; PARP-inhibitor; olaparib; DNA-damage; gold quantum dots; plasma; nanomaterials; cellular uptake; invasiveness; cold atmospheric pressure plasma; plasma-activated Ringer’s lactate solution; ovarian cancer; cytotoxicity; plasma-activated liquids; multicellular tumor spheroids; long-lived reactive oxygen and nitrogen species; high frequency electrosurgery; plasma treatment; cold atmospheric plasma (CAP); free radicals; cancer selectivity; cervical cancer treatment; cervical intraepithelial neoplasia; cholangiocarcinoma; cold plasma; innovative therapy; tumor cells; macrophages; plasma selectivity; plasma jet; n/a