dc.contributor.author | Wigner, Paulina | |
dc.contributor.author | Zielinski, Krzysztof | |
dc.contributor.author | Łabieniec-Watała, Magdalena | |
dc.contributor.author | Marczak, Agnieszka | |
dc.contributor.author | Szwed, Marzena | |
dc.date.accessioned | 2021-12-16T11:58:43Z | |
dc.date.available | 2021-12-16T11:58:43Z | |
dc.date.issued | 2021 | |
dc.identifier.citation | Wigner, P., Zielinski, K., Labieniec-Watala, M. et al. Doxorubicin–transferrin conjugate alters mitochondrial homeostasis and energy metabolism in human breast cancer cells. Sci Rep 11, 4544 (2021). https://doi.org/10.1038/s41598-021-84146-4 | pl_PL |
dc.identifier.uri | http://hdl.handle.net/11089/40077 | |
dc.description.abstract | Doxorubicin (DOX) is considered one of the most powerful chemotherapeutic agents but its clinical use has several limitations, including cardiomyopathy and cellular resistance to the drug. By using transferrin (Tf) as a drug carrier, however, the adverse effects of doxorubicin as well as drug resistance can be reduced. The main objective of this study was to determine the exact nature and extent to which mitochondrial function is influenced by DOX–Tf conjugate treatment, specifically in human breast adenocarcinoma cells. We assessed the potential of DOX–Tf conjugate as a drug delivery system, monitoring its cytotoxicity using the MTT assay and ATP measurements. Moreover, we measured the alterations of mitochondrial function and oxidative stress markers. The effect of DOX–Tf was the most pronounced in MDA-MB-231, triple-negative breast cancer cells, whereas non-cancer endothelial HUVEC-ST cells were more resistant to DOX–Tf conjugate than to free DOX treatment. A different sensitivity of two investigate breast cancer cell lines corresponded to the functionality of their cellular antioxidant systems and expression of estrogen receptors. Our data also revealed that conjugate treatment mediated free radical generation and altered the mitochondrial bioenergetics in breast cancer cells. | pl_PL |
dc.description.sponsorship | This work was supported in part by Grant No. B1511000001026.02 of the University of Lodz, Poland. | pl_PL |
dc.language.iso | en | pl_PL |
dc.publisher | Springer Nature | pl_PL |
dc.relation.ispartofseries | Scientific Reports;11 | |
dc.rights | Uznanie autorstwa 4.0 Międzynarodowe | * |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.subject | biochemistry | pl_PL |
dc.subject | biophysics | pl_PL |
dc.subject | biotechnology | pl_PL |
dc.subject | cancer | pl_PL |
dc.subject | cell biology | pl_PL |
dc.subject | chemical biology | pl_PL |
dc.subject | drug discovery | pl_PL |
dc.subject | molecular biology | pl_PL |
dc.title | Doxorubicin–transferrin conjugate alters mitochondrial homeostasis and energy metabolism in human breast cancer cells | pl_PL |
dc.type | Article | pl_PL |
dc.page.number | 14 | pl_PL |
dc.contributor.authorAffiliation | Department of Medical Biophysics, Institute of Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland | pl_PL |
dc.contributor.authorAffiliation | Department of Medical Biophysics, Institute of Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland | pl_PL |
dc.contributor.authorAffiliation | Department of Medical Biophysics, Institute of Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland | pl_PL |
dc.contributor.authorAffiliation | Department of Medical Biophysics, Institute of Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland | pl_PL |
dc.contributor.authorAffiliation | Department of Medical Biophysics, Institute of Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland | pl_PL |
dc.identifier.eissn | 2045-2322 | |
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dc.identifier.doi | 10.1038/s41598-021-84146-4 | |
dc.relation.volume | 4544 | pl_PL |
dc.discipline | nauki biologiczne | pl_PL |