Exploiting zebrafish xenografts for testing the in vivo antitumorigenic activity of microcin E492 against human colorectal cancer cells
Author
dc.contributor.author
Varas Poblete, Macarena
Author
dc.contributor.author
Muñoz Montecinos, Carlos
Author
dc.contributor.author
Kallens, Violeta
Author
dc.contributor.author
Simon Zegers, María Valeska
Author
dc.contributor.author
Allende Connelly, Miguel
Author
dc.contributor.author
Marcoleta Caldera, Andrés
Author
dc.contributor.author
Lagos Mónaco, Rosalba
Admission date
dc.date.accessioned
2020-05-15T16:30:24Z
Available date
dc.date.available
2020-05-15T16:30:24Z
Publication date
dc.date.issued
2020
Cita de ítem
dc.identifier.citation
Frontiers in Microbiology (2020) 11: article 405
es_ES
Identifier
dc.identifier.other
10.3389/fmicb.2020.00405
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/174763
Abstract
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One of the approaches to address cancer treatment is to develop new drugs not only to obtain compounds with less side effects, but also to have a broader set of alternatives to tackle the resistant forms of this pathology. In this regard, growing evidence supports the use of bacteria-derived peptides such as bacteriocins, which have emerged as promising anti-cancer molecules. In addition to test the activity of these molecules on cancer cells in culture, their in vivo antitumorigenic properties must be validated in animal models. Although the standard approach for such assays employs experiments in nude mice, at the initial stages of testing, the use of high-throughput animal models would permit rapid proof-of-concept experiments, screening a high number of compounds, and thus increasing the possibilities of finding new anti-cancer molecules. A validated and promising alternative animal model are zebrafish larvae harboring xenografts of human cancer cells. Here, we addressed the anti-cancer properties of the antibacterial peptide microcin E492 (MccE492), a bacteriocin produced by Klebsiella pneumoniae, showing that this peptide has a marked cytotoxic effect on human colorectal cancer cells in vitro. Furthermore, we developed a zebrafish xenograft model using these cells to test the antitumor effect of MccE492 in vivo, demonstrating that intratumor injection of this peptide significantly reduced the tumor cell mass. Our results provide, for the first time, evidence of the in vivo antitumoral properties of a bacteriocin tested in an animal model. This evidence strongly supports the potential of this bacteriocin for the development of novel anti-cancer therapies.
es_ES
Patrocinador
dc.description.sponsorship
Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT)
CONICYT FONDECYT
1140430
3170449
FONDAP
15090007