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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7824363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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