The Novel 5-Fluorouracil Loaded Ruthenium-based Nanocarriers Enhanced Anticancer and Apoptotic Efficiency while Reducing Multidrug Resistance in Colorectal Cancer Cells

ArticleAçık Erişim

Özet

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. © 2023, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/12227Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1007/s10895-023-03180-9Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorDanişman-Kalindemirtaş, Ferdane
dc.contributor.authorÖzerkan, Dilşad
dc.contributor.authorKariper, İshak Afşin
dc.contributor.authorBulut, Huri
dc.date.accessioned2026-10-18T20:27:09.144497839Z
dc.date.available2026-10-18T20:27:09.144497839Z
dc.date.issued2023
dc.description.abstractRecently, 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. © 2023, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
dc.identifier.doi10.1007/s10895-023-03180-9
dc.identifier.eissn1573-4994
dc.identifier.endpage1236
dc.identifier.issn1053-0509
dc.identifier.issue3
dc.identifier.pmid36811696
dc.identifier.scopus2-s2.0-85148522595
dc.identifier.startpage1227
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12227
dc.identifier.volume33
dc.identifier.wosWOS:000936252100002
dc.language.isoen
dc.publisherSpringer
dc.relation.ispartofJournal of Fluorescence
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subject5FU
dc.subjectApoptosis
dc.subjectColorectal cancer
dc.subjectCytotoxicity
dc.subjectRuthenium-based nanoparticles
dc.subjectAntineoplastic Agents
dc.subjectATP Binding Cassette Transporter, Subfamily G, Member 2
dc.subjectCell Line, Tumor
dc.subjectColorectal Neoplasms
dc.subjectFluorouracil
dc.subjectHCT116 Cells
dc.subjectHumans
dc.subjectNeoplasm Proteins
dc.subjectRuthenium
dc.subjectCancer cells
dc.subjectCell culture
dc.subjectDiseases
dc.subjectGene expression
dc.subjectantineoplastic agent
dc.subjectbreast cancer resistance protein
dc.subjecttumor protein
dc.subject5-fluorouracil
dc.subjectCell-be
dc.subjectCell/B.E
dc.subjectCell/BE
dc.subjectColorectal cancer cell
dc.subjectCytotoxic effects
dc.subjectMultidrug resistance
dc.subjectNanocarriers
dc.subjectRuthenium-based nanoparticle
dc.titleThe Novel 5-Fluorouracil Loaded Ruthenium-based Nanocarriers Enhanced Anticancer and Apoptotic Efficiency while Reducing Multidrug Resistance in Colorectal Cancer Cells
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus4
rdl.citation.wos4
rdl.departmentFaculty of Medicine, Department of Physiology, Erzincan Binali Yıldırım University, Erzincan, Turkey.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)