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The Cytotoxicity of RNase-Derived Peptides

Bacterial ribonuclease binase exhibits a cytotoxic effect on tumor cells possessing certain oncogenes. The aim of this study was to identify the structural parts of the binase molecule that exert cytotoxicity. Out of five designed peptides, the peptides representing the binase regions 21–50 and 74–9...

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Autores principales: Ulyanova, Vera, Dudkina, Elena, Nadyrova, Alsu, Kalashnikov, Vladimir, Surchenko, Yulia, Ilinskaya, Olga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824363/
https://www.ncbi.nlm.nih.gov/pubmed/33375305
http://dx.doi.org/10.3390/biom11010016
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author Ulyanova, Vera
Dudkina, Elena
Nadyrova, Alsu
Kalashnikov, Vladimir
Surchenko, Yulia
Ilinskaya, Olga
author_facet Ulyanova, Vera
Dudkina, Elena
Nadyrova, Alsu
Kalashnikov, Vladimir
Surchenko, Yulia
Ilinskaya, Olga
author_sort Ulyanova, Vera
collection PubMed
description Bacterial ribonuclease binase exhibits a cytotoxic effect on tumor cells possessing certain oncogenes. The aim of this study was to identify the structural parts of the binase molecule that exert cytotoxicity. Out of five designed peptides, the peptides representing the binase regions 21–50 and 74–94 have the highest cytotoxic potential toward human cervical HeLa and breast BT-20 and MCF-7 cancer cells. The peptides B21–50 and B74–94 were not able to enter human lung adenocarcinoma A549 cells, unlike BT-20 cells, explaining their failure to inhibit A549 cell proliferation. The peptide B74–94 shares similarities with epidermal growth factor (EGF), suggesting the peptide’s specificity for EGF receptor overexpressed in BT-20 cells. Thus, the binase-derived peptides have the potential of being further developed as tumor-targeting peptides.
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spelling pubmed-78243632021-01-24 The Cytotoxicity of RNase-Derived Peptides Ulyanova, Vera Dudkina, Elena Nadyrova, Alsu Kalashnikov, Vladimir Surchenko, Yulia Ilinskaya, Olga Biomolecules Article Bacterial ribonuclease binase exhibits a cytotoxic effect on tumor cells possessing certain oncogenes. The aim of this study was to identify the structural parts of the binase molecule that exert cytotoxicity. Out of five designed peptides, the peptides representing the binase regions 21–50 and 74–94 have the highest cytotoxic potential toward human cervical HeLa and breast BT-20 and MCF-7 cancer cells. The peptides B21–50 and B74–94 were not able to enter human lung adenocarcinoma A549 cells, unlike BT-20 cells, explaining their failure to inhibit A549 cell proliferation. The peptide B74–94 shares similarities with epidermal growth factor (EGF), suggesting the peptide’s specificity for EGF receptor overexpressed in BT-20 cells. Thus, the binase-derived peptides have the potential of being further developed as tumor-targeting peptides. MDPI 2020-12-26 /pmc/articles/PMC7824363/ /pubmed/33375305 http://dx.doi.org/10.3390/biom11010016 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ulyanova, Vera
Dudkina, Elena
Nadyrova, Alsu
Kalashnikov, Vladimir
Surchenko, Yulia
Ilinskaya, Olga
The Cytotoxicity of RNase-Derived Peptides
title The Cytotoxicity of RNase-Derived Peptides
title_full The Cytotoxicity of RNase-Derived Peptides
title_fullStr The Cytotoxicity of RNase-Derived Peptides
title_full_unstemmed The Cytotoxicity of RNase-Derived Peptides
title_short The Cytotoxicity of RNase-Derived Peptides
title_sort cytotoxicity of rnase-derived peptides
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824363/
https://www.ncbi.nlm.nih.gov/pubmed/33375305
http://dx.doi.org/10.3390/biom11010016
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