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Assessing the Antitumor Potential of Variants of the Extracellular Carbohydrate Polymer from Synechocystis ΔsigF Mutant

Cancer is a leading cause of death worldwide with a huge societal and economic impact. Clinically effective and less expensive anticancer agents derived from natural sources can help to overcome limitations and negative side effects of chemotherapy and radiotherapy. Previously, we showed that the ex...

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Autores principales: Mota, Rita, Lima, Raquel T., Flores, Carlos, Silva, Juliana F., Cruz, Beatriz, Alves, Bárbara, Pinto, Marta T., Adessi, Alessandra, Pereira, Sara B., De Philippis, Roberto, Soares, Paula, Tamagnini, Paula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057057/
https://www.ncbi.nlm.nih.gov/pubmed/36987163
http://dx.doi.org/10.3390/polym15061382
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author Mota, Rita
Lima, Raquel T.
Flores, Carlos
Silva, Juliana F.
Cruz, Beatriz
Alves, Bárbara
Pinto, Marta T.
Adessi, Alessandra
Pereira, Sara B.
De Philippis, Roberto
Soares, Paula
Tamagnini, Paula
author_facet Mota, Rita
Lima, Raquel T.
Flores, Carlos
Silva, Juliana F.
Cruz, Beatriz
Alves, Bárbara
Pinto, Marta T.
Adessi, Alessandra
Pereira, Sara B.
De Philippis, Roberto
Soares, Paula
Tamagnini, Paula
author_sort Mota, Rita
collection PubMed
description Cancer is a leading cause of death worldwide with a huge societal and economic impact. Clinically effective and less expensive anticancer agents derived from natural sources can help to overcome limitations and negative side effects of chemotherapy and radiotherapy. Previously, we showed that the extracellular carbohydrate polymer of a Synechocystis ΔsigF overproducing mutant displayed a strong antitumor activity towards several human tumor cell lines, by inducing high levels of apoptosis through p53 and caspase-3 activation. Here, the ΔsigF polymer was manipulated to obtain variants that were tested in a human melanoma (Mewo) cell line. Our results demonstrated that high molecular mass fractions were important for the polymer bioactivity, and that the reduction of the peptide content generated a variant with enhanced in vitro antitumor activity. This variant, and the original ΔsigF polymer, were further tested in vivo using the chick chorioallantoic membrane (CAM) assay. Both polymers significantly decreased xenografted CAM tumor growth and affected tumor morphology, by promoting less compact tumors, validating their antitumor potential in vivo. This work contributes with strategies for the design and testing tailored cyanobacterial extracellular polymers and further strengths the relevance of evaluating this type of polymers for biotechnological/biomedical applications.
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spelling pubmed-100570572023-03-30 Assessing the Antitumor Potential of Variants of the Extracellular Carbohydrate Polymer from Synechocystis ΔsigF Mutant Mota, Rita Lima, Raquel T. Flores, Carlos Silva, Juliana F. Cruz, Beatriz Alves, Bárbara Pinto, Marta T. Adessi, Alessandra Pereira, Sara B. De Philippis, Roberto Soares, Paula Tamagnini, Paula Polymers (Basel) Article Cancer is a leading cause of death worldwide with a huge societal and economic impact. Clinically effective and less expensive anticancer agents derived from natural sources can help to overcome limitations and negative side effects of chemotherapy and radiotherapy. Previously, we showed that the extracellular carbohydrate polymer of a Synechocystis ΔsigF overproducing mutant displayed a strong antitumor activity towards several human tumor cell lines, by inducing high levels of apoptosis through p53 and caspase-3 activation. Here, the ΔsigF polymer was manipulated to obtain variants that were tested in a human melanoma (Mewo) cell line. Our results demonstrated that high molecular mass fractions were important for the polymer bioactivity, and that the reduction of the peptide content generated a variant with enhanced in vitro antitumor activity. This variant, and the original ΔsigF polymer, were further tested in vivo using the chick chorioallantoic membrane (CAM) assay. Both polymers significantly decreased xenografted CAM tumor growth and affected tumor morphology, by promoting less compact tumors, validating their antitumor potential in vivo. This work contributes with strategies for the design and testing tailored cyanobacterial extracellular polymers and further strengths the relevance of evaluating this type of polymers for biotechnological/biomedical applications. MDPI 2023-03-10 /pmc/articles/PMC10057057/ /pubmed/36987163 http://dx.doi.org/10.3390/polym15061382 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mota, Rita
Lima, Raquel T.
Flores, Carlos
Silva, Juliana F.
Cruz, Beatriz
Alves, Bárbara
Pinto, Marta T.
Adessi, Alessandra
Pereira, Sara B.
De Philippis, Roberto
Soares, Paula
Tamagnini, Paula
Assessing the Antitumor Potential of Variants of the Extracellular Carbohydrate Polymer from Synechocystis ΔsigF Mutant
title Assessing the Antitumor Potential of Variants of the Extracellular Carbohydrate Polymer from Synechocystis ΔsigF Mutant
title_full Assessing the Antitumor Potential of Variants of the Extracellular Carbohydrate Polymer from Synechocystis ΔsigF Mutant
title_fullStr Assessing the Antitumor Potential of Variants of the Extracellular Carbohydrate Polymer from Synechocystis ΔsigF Mutant
title_full_unstemmed Assessing the Antitumor Potential of Variants of the Extracellular Carbohydrate Polymer from Synechocystis ΔsigF Mutant
title_short Assessing the Antitumor Potential of Variants of the Extracellular Carbohydrate Polymer from Synechocystis ΔsigF Mutant
title_sort assessing the antitumor potential of variants of the extracellular carbohydrate polymer from synechocystis δsigf mutant
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057057/
https://www.ncbi.nlm.nih.gov/pubmed/36987163
http://dx.doi.org/10.3390/polym15061382
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