Yayın: The Novel 5-Fluorouracil Loaded Ruthenium-based Nanocarriers Enhanced Anticancer and Apoptotic Efficiency while Reducing Multidrug Resistance in Colorectal Cancer Cells
| dc.contributor.author | Danisman-Kalindemirtas, Ferdane | |
| dc.contributor.author | Ozerkan, Dilsad | |
| dc.contributor.author | Kariper, Ishak Afsin | |
| dc.contributor.author | Bulut, Huri | |
| dc.date.accessioned | 2026-01-05T23:15:43Z | |
| dc.date.issued | 2023-02-22 | |
| dc.description.abstract | Recently, nanocarriers have been made to eliminate the disadvantages of chemotherapeutic agents by nanocarriers. Nanocarriers show their efficacy through their targeted and controlled release. In this study, 5-fluorouracil (5FU) was loaded into ruthenium (Ru)-based nanocarrier (5FU-RuNPs) for the first time to eliminate the disadvantages of 5FU, and its cytotoxic and apoptotic effects on HCT116 colorectal cancer cells were compared with free 5FU. 5FU-RuNPs with a size of approximately 100 nm showed a 2.61-fold higher cytotoxic effect compared to free 5FU. Apoptotic cells were detected by Hoechst/propidium iodide double staining, and the expression levels of BAX/Bcl-2 and p53 proteins, in which apoptosis occurred intrinsically, were revealed. In addition, 5FU-RuNPs was also found to reduce multidrug resistance (MDR) according to BCRP/ABCG2 gene expression levels. When all the results were evaluated, the fact that Ru-based nanocarriers alone did not cause cytotoxicity proved that they were ideal nanocarriers. Moreover, 5FU-RuNPs did not show any significant effect on the cell viability of normal human epithelial cell lines BEAS-2B. Consequently, the 5FU-RuNPs synthesized for the first time may be ideal candidates for cancer treatment because they can minimize the potential drawbacks of free 5FU. | |
| dc.description.uri | https://doi.org/10.1007/s10895-023-03180-9 | |
| dc.description.uri | https://pubmed.ncbi.nlm.nih.gov/36811696 | |
| dc.description.uri | https://avesis.erciyes.edu.tr/publication/details/1bec02e3-529f-40c2-b245-e4ff41e01d89/oai | |
| dc.description.uri | https://hdl.handle.net/20.500.12713/5549 | |
| dc.identifier.doi | 10.1007/s10895-023-03180-9 | |
| dc.identifier.eissn | 1573-4994 | |
| dc.identifier.endpage | 1236 | |
| dc.identifier.issn | 1053-0509 | |
| dc.identifier.openaire | doi_dedup___::98a513baa16ebde1b719062fd98730e3 | |
| dc.identifier.pubmed | 36811696 | |
| dc.identifier.scopus | 2-s2.0-85148522595 | |
| dc.identifier.startpage | 1227 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12597/43676 | |
| dc.identifier.volume | 33 | |
| dc.identifier.wos | 000936252100002 | |
| dc.language.iso | eng | |
| dc.publisher | Springer Science and Business Media LLC | |
| dc.relation.ispartof | Journal of Fluorescence | |
| dc.rights | CLOSED | |
| dc.subject | Colorectal Cancer | |
| dc.subject | Ruthenium-Based Nanoparticles | |
| dc.subject | Cytotoxicity | |
| dc.subject | Antineoplastic Agents | |
| dc.subject | Apoptosis | |
| dc.subject | HCT116 Cells | |
| dc.subject | Ruthenium | |
| dc.subject | Neoplasm Proteins | |
| dc.subject | Cell Line, Tumor | |
| dc.subject | Humans | |
| dc.subject | ATP Binding Cassette Transporter, Subfamily G, Member 2 | |
| dc.subject | Fluorouracil | |
| dc.subject | Colorectal Neoplasms | |
| dc.subject | fu | |
| dc.subject.sdg | 3. Good health | |
| dc.title | The Novel 5-Fluorouracil Loaded Ruthenium-based Nanocarriers Enhanced Anticancer and Apoptotic Efficiency while Reducing Multidrug Resistance in Colorectal Cancer Cells | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
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| local.import.source | OpenAire | |
| local.indexed.at | WOS | |
| local.indexed.at | Scopus | |
| local.indexed.at | PubMed |
