Deciphering the genotoxic and cytotoxic properties of teicoplanin: a combined laboratory and computational investigation
dc.authorid | Berber, Ahmet Ali / 0000-0002-2036-6929 | |
dc.authorid | Alıravcı, Işıl Deniz / 0000-0002-4740-1579 | |
dc.authorid | Akıncı Kenanoğlu, Nihan / 0000-0002-3917-6412 | |
dc.contributor.author | Berber, Ahmet Ali | |
dc.contributor.author | Alıravcı, Işıl Deniz | |
dc.contributor.author | Akıncı Kenanoğlu, Nihan | |
dc.contributor.author | Demir, Şefika Nur | |
dc.date.accessioned | 2025-05-29T02:57:46Z | |
dc.date.available | 2025-05-29T02:57:46Z | |
dc.date.issued | 2025 | |
dc.department | Çanakkale Onsekiz Mart Üniversitesi | |
dc.description.abstract | In this study, the mutagenicity and carcinogenicity of the teicoplanin antibiotic were first investigated using the Vega Hub and Toxtree software through in silico prediction. The cytotoxic and genotoxic effects were evaluated using in vitro assays, including the mitotic index (MI), micronucleus (MN), nuclear division index (NDI), and Comet Assay (CA) in human lymphocytes. In the in vitro studies, both 24-hour and 48-hour exposures were conducted for MI, and teicoplanin significantly decreased MI compared to the control at all concentrations. In addition, a significant increase was detected in the MN frequency compared to the negative control at all concentrations. In the Comet assay, tail length significantly increased compared to the control at all concentrations except for 5.6 mu g/mL, while tail moment and comet tail intensity significantly increased at all concentrations compared to the control. In conclusion, within the concentration range used in this study, teicoplanin was found to have cytotoxic and genotoxic effects. | |
dc.description.sponsorship | Scientific Research Projects coordination unit of Canakkale Onsekiz Mart university [thD-2022-3964] | |
dc.description.sponsorship | this study was supported by the Scientific Research Projects coordination unit of Canakkale Onsekiz Mart university under project number thD-2022-3964. | |
dc.identifier.doi | 10.1080/01480545.2025.2502446 | |
dc.identifier.issn | 0148-0545 | |
dc.identifier.issn | 1525-6014 | |
dc.identifier.pmid | 40337791 | |
dc.identifier.scopus | 2-s2.0-105004431993 | |
dc.identifier.scopusquality | Q1 | |
dc.identifier.uri | https://doi.org/10.1080/01480545.2025.2502446 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12428/30173 | |
dc.identifier.wos | WOS:001484065700001 | |
dc.identifier.wosquality | Q3 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | |
dc.publisher | Taylor & Francis Ltd | |
dc.relation.ispartof | Drug and Chemical Toxicology | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.snmz | KA_WOS_20250529 | |
dc.subject | Genotoxicity | |
dc.subject | cytotoxicity | |
dc.subject | micronucleus | |
dc.subject | mitotic index | |
dc.subject | comet | |
dc.subject | teicoplanin | |
dc.subject | in silico | |
dc.title | Deciphering the genotoxic and cytotoxic properties of teicoplanin: a combined laboratory and computational investigation | |
dc.type | Article |
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