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Botulinum toxin in cancer therapy—current perspectives and limitations

ABSTRACT: Different serotypes of botulinum toxins (BoNTs) act upon different types of SNARE proteins. This property is used in aesthetic medicine to treat certain eye disorders such as crossed eyes (strabismus) and uncontrolled blinking (blepharospasm), to treat muscle spasms or movement disorders,...

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Autores principales: Grenda, Tomasz, Grenda, Anna, Krawczyk, Paweł, Kwiatek, Krzysztof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8763801/
https://www.ncbi.nlm.nih.gov/pubmed/34951660
http://dx.doi.org/10.1007/s00253-021-11741-w
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author Grenda, Tomasz
Grenda, Anna
Krawczyk, Paweł
Kwiatek, Krzysztof
author_facet Grenda, Tomasz
Grenda, Anna
Krawczyk, Paweł
Kwiatek, Krzysztof
author_sort Grenda, Tomasz
collection PubMed
description ABSTRACT: Different serotypes of botulinum toxins (BoNTs) act upon different types of SNARE proteins. This property is used in aesthetic medicine to treat certain eye disorders such as crossed eyes (strabismus) and uncontrolled blinking (blepharospasm), to treat muscle spasms or movement disorders, and, for the two last decades, more and more often, to provide support in cancer therapy, especially so as to obtain analgesic effects upon spastic conditions. The limited literature data also suggests that the addition of BoNTs to the culture of cancer cell lines reduces cell growth, and mitotic activity, and promotes their apoptosis. BoNTs have several advantages that can be emphasized: BoNTs act on both perfusion and oxygenation; moreover, BoNTs are considered to be safe and free of systemic side effects upon administration. Recently, advances in molecular biology techniques have allowed a wide variety of novel BoNT constructs with alternative functions. These constructs could be assessed as potential new classes of anti-cancer drugs. This creates new potential perspectives in the wider use of non-toxic modified BoNT constructs in cancer therapy. In the light of the mentioned premises and existing literature reports, the aim of this review is to summarize current data and reports considering BoNT use in cancer therapy. KEY POINTS: •Botulinum toxin (BoNTs) may be useful in cancer treatment. •Botulinum toxin can serve as an analgesic after cancer radiotherapy. •Botulinum toxin has the ability to inhibit tumor growth and promote apoptosis of neoplastic cells.
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spelling pubmed-87638012022-01-31 Botulinum toxin in cancer therapy—current perspectives and limitations Grenda, Tomasz Grenda, Anna Krawczyk, Paweł Kwiatek, Krzysztof Appl Microbiol Biotechnol Mini-Review ABSTRACT: Different serotypes of botulinum toxins (BoNTs) act upon different types of SNARE proteins. This property is used in aesthetic medicine to treat certain eye disorders such as crossed eyes (strabismus) and uncontrolled blinking (blepharospasm), to treat muscle spasms or movement disorders, and, for the two last decades, more and more often, to provide support in cancer therapy, especially so as to obtain analgesic effects upon spastic conditions. The limited literature data also suggests that the addition of BoNTs to the culture of cancer cell lines reduces cell growth, and mitotic activity, and promotes their apoptosis. BoNTs have several advantages that can be emphasized: BoNTs act on both perfusion and oxygenation; moreover, BoNTs are considered to be safe and free of systemic side effects upon administration. Recently, advances in molecular biology techniques have allowed a wide variety of novel BoNT constructs with alternative functions. These constructs could be assessed as potential new classes of anti-cancer drugs. This creates new potential perspectives in the wider use of non-toxic modified BoNT constructs in cancer therapy. In the light of the mentioned premises and existing literature reports, the aim of this review is to summarize current data and reports considering BoNT use in cancer therapy. KEY POINTS: •Botulinum toxin (BoNTs) may be useful in cancer treatment. •Botulinum toxin can serve as an analgesic after cancer radiotherapy. •Botulinum toxin has the ability to inhibit tumor growth and promote apoptosis of neoplastic cells. Springer Berlin Heidelberg 2021-12-24 2022 /pmc/articles/PMC8763801/ /pubmed/34951660 http://dx.doi.org/10.1007/s00253-021-11741-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Mini-Review
Grenda, Tomasz
Grenda, Anna
Krawczyk, Paweł
Kwiatek, Krzysztof
Botulinum toxin in cancer therapy—current perspectives and limitations
title Botulinum toxin in cancer therapy—current perspectives and limitations
title_full Botulinum toxin in cancer therapy—current perspectives and limitations
title_fullStr Botulinum toxin in cancer therapy—current perspectives and limitations
title_full_unstemmed Botulinum toxin in cancer therapy—current perspectives and limitations
title_short Botulinum toxin in cancer therapy—current perspectives and limitations
title_sort botulinum toxin in cancer therapy—current perspectives and limitations
topic Mini-Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8763801/
https://www.ncbi.nlm.nih.gov/pubmed/34951660
http://dx.doi.org/10.1007/s00253-021-11741-w
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