Cold argon plasma as adjuvant tumour therapy on progressive head and neck cancer: A preclinical study

dc.bibliographicCitation.firstPage2061
dc.bibliographicCitation.issue10
dc.bibliographicCitation.journalTitleApplied Scienceseng
dc.bibliographicCitation.volume9
dc.contributor.authorHasse, Sybille
dc.contributor.authorSeebauer, Christian
dc.contributor.authorWende, Kristian
dc.contributor.authorSchmidt, Anke
dc.contributor.authorMetelmann, Hans-Robert
dc.contributor.authorWoedtke, Thomas von
dc.contributor.authorBekeschus, Sander
dc.date.accessioned2022-12-05T09:41:59Z
dc.date.available2022-12-05T09:41:59Z
dc.date.issued2019
dc.description.abstractInvestigating cold argon plasma (CAP) for medical applications is a rapidly growing, innovative field of research. The controllable supply of reactive oxygen and nitrogen species through CAP has the potential for utilization in tumour treatment. Maxillofacial surgery is limited if tumours grow on vital structures such as the arteria carotis. Here CAP could be considered as an option for adjuvant intraoperative tumour therapy especially in the case of squamous cell carcinoma of the head and neck. Further preclinical research is necessary to investigate the efficacy of this technology for future clinical applications in cancer treatment. Initially, a variety of in vitro assays was performed on two cell lines that served as surrogate for the squamous cell carcinoma (SCC) and healthy tissue, respectively. Cell viability, motility and the activation of apoptosis in SCC cells (HNO97) was compared with those in normal HaCaT keratinocytes. In addition, induction of apoptosis in ex vivo CAP treated human tissue biopsies of patients with tumours of the head and neck was monitored and compared to healthy control tissue of the same patient. In response to CAP treatment, normal HaCaT keratinocytes differed significantly from their malignant counterpart HNO97 cells in cell motility only whereas cell viability remained similar. Moreover, CAP treatment of tumour tissue induced more apoptotic cells than in healthy tissue that was accompanied by elevated extracellular cytochrome c levels. This study promotes a future role of CAP as an adjuvant intraoperative tumour therapy option in the treatment of head and neck cancer. Moreover, patient-derived tissue explants complement in vitro examinations in a meaningful way to reflect an antitumoral role of CAP. © 2019 by the authors.eng
dc.description.versionpublishedVersion
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/10504
dc.identifier.urihttp://dx.doi.org/10.34657/9540
dc.language.isoeng
dc.publisherBasel : MDPI
dc.relation.doihttps://doi.org/10.3390/app9102061
dc.relation.essn2076-3417
dc.rights.licenseCC BY 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc600
dc.subject.otherApoptosiseng
dc.subject.otherCold argon plasmaeng
dc.subject.otherHead and neck squamous cell carcinomaeng
dc.subject.otherKeratinocyteseng
dc.subject.otherPlasma medicineeng
dc.titleCold argon plasma as adjuvant tumour therapy on progressive head and neck cancer: A preclinical studyeng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccess
wgl.contributorINP
wgl.subjectMedizin, Gesundheitger
wgl.typeZeitschriftenartikelger
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