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A zebrafish HCT116 xenograft model to predict anandamide outcomes on colorectal cancer

Colon cancer is one of the leading causes of death worldwide. In recent years, cannabinoids have been extensively studied for their potential anticancer effects and symptom management. Several in vitro studies reported anandamide’s (AEA) ability to block cancer cell proliferation and migration, but...

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Autores principales: Maradonna, Francesca, Fontana, Camilla M., Sella, Fiorenza, Giommi, Christian, Facchinello, Nicola, Rampazzo, Chiara, Caichiolo, Micol, Hoseinifar, Seyed Hossein, Dalla Valle, Luisa, Van Doan, Hien, Carnevali, Oliana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789132/
https://www.ncbi.nlm.nih.gov/pubmed/36564370
http://dx.doi.org/10.1038/s41419-022-05523-z
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author Maradonna, Francesca
Fontana, Camilla M.
Sella, Fiorenza
Giommi, Christian
Facchinello, Nicola
Rampazzo, Chiara
Caichiolo, Micol
Hoseinifar, Seyed Hossein
Dalla Valle, Luisa
Van Doan, Hien
Carnevali, Oliana
author_facet Maradonna, Francesca
Fontana, Camilla M.
Sella, Fiorenza
Giommi, Christian
Facchinello, Nicola
Rampazzo, Chiara
Caichiolo, Micol
Hoseinifar, Seyed Hossein
Dalla Valle, Luisa
Van Doan, Hien
Carnevali, Oliana
author_sort Maradonna, Francesca
collection PubMed
description Colon cancer is one of the leading causes of death worldwide. In recent years, cannabinoids have been extensively studied for their potential anticancer effects and symptom management. Several in vitro studies reported anandamide’s (AEA) ability to block cancer cell proliferation and migration, but evidence from in vivo studies is still lacking. Thus, in this study, the effects of AEA exposure in zebrafish embryos transplanted with HCT116 cells were evaluated. Totally, 48 hpf xenografts were exposed to 10 nM AEA, 10 nM AM251, one of the cannabinoid 1 receptor (CB1) antagonist/inverse agonists, and to AEA + AM251, to verify the specific effect of AEA treatment. AEA efficacy was evaluated by confocal microscopy, which demonstrated that these xenografts presented a smaller tumor size, reduced tumor angiogenesis, and lacked micrometastasis formation. To gain deeper evidence into AEA action, microscopic observations were completed by molecular analyses. RNA seq performed on zebrafish transcriptome reported the downregulation of genes involved in cell proliferation, angiogenesis, and the immune system. Conversely, HCT116 cell transcripts resulted not affected by AEA treatment. In vitro HCT116 culture, in fact, confirmed that AEA exposure did not affect cell proliferation and viability, thus suggesting that the reduced tumor size mainly depends on direct effects on the fish rather than on the transplanted cancer cells. AEA reduced cell proliferation and tumor angiogenesis, as suggested by socs3 and pcnp mRNAs and Vegfc protein levels, and exerted anti-inflammatory activity, as indicated by the reduction of il-11a, mhc1uba, and csf3b mRNA. Of note, are the results obtained in groups exposed to AM251, which presence nullifies AEA’s beneficial effects. In conclusion, this study promotes the efficacy of AEA in personalized cancer therapy, as suggested by its ability to drive tumor growth and metastasis, and strongly supports the use of zebrafish xenograft as an emerging model platform for cancer studies.
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spelling pubmed-97891322022-12-25 A zebrafish HCT116 xenograft model to predict anandamide outcomes on colorectal cancer Maradonna, Francesca Fontana, Camilla M. Sella, Fiorenza Giommi, Christian Facchinello, Nicola Rampazzo, Chiara Caichiolo, Micol Hoseinifar, Seyed Hossein Dalla Valle, Luisa Van Doan, Hien Carnevali, Oliana Cell Death Dis Article Colon cancer is one of the leading causes of death worldwide. In recent years, cannabinoids have been extensively studied for their potential anticancer effects and symptom management. Several in vitro studies reported anandamide’s (AEA) ability to block cancer cell proliferation and migration, but evidence from in vivo studies is still lacking. Thus, in this study, the effects of AEA exposure in zebrafish embryos transplanted with HCT116 cells were evaluated. Totally, 48 hpf xenografts were exposed to 10 nM AEA, 10 nM AM251, one of the cannabinoid 1 receptor (CB1) antagonist/inverse agonists, and to AEA + AM251, to verify the specific effect of AEA treatment. AEA efficacy was evaluated by confocal microscopy, which demonstrated that these xenografts presented a smaller tumor size, reduced tumor angiogenesis, and lacked micrometastasis formation. To gain deeper evidence into AEA action, microscopic observations were completed by molecular analyses. RNA seq performed on zebrafish transcriptome reported the downregulation of genes involved in cell proliferation, angiogenesis, and the immune system. Conversely, HCT116 cell transcripts resulted not affected by AEA treatment. In vitro HCT116 culture, in fact, confirmed that AEA exposure did not affect cell proliferation and viability, thus suggesting that the reduced tumor size mainly depends on direct effects on the fish rather than on the transplanted cancer cells. AEA reduced cell proliferation and tumor angiogenesis, as suggested by socs3 and pcnp mRNAs and Vegfc protein levels, and exerted anti-inflammatory activity, as indicated by the reduction of il-11a, mhc1uba, and csf3b mRNA. Of note, are the results obtained in groups exposed to AM251, which presence nullifies AEA’s beneficial effects. In conclusion, this study promotes the efficacy of AEA in personalized cancer therapy, as suggested by its ability to drive tumor growth and metastasis, and strongly supports the use of zebrafish xenograft as an emerging model platform for cancer studies. Nature Publishing Group UK 2022-12-23 /pmc/articles/PMC9789132/ /pubmed/36564370 http://dx.doi.org/10.1038/s41419-022-05523-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Maradonna, Francesca
Fontana, Camilla M.
Sella, Fiorenza
Giommi, Christian
Facchinello, Nicola
Rampazzo, Chiara
Caichiolo, Micol
Hoseinifar, Seyed Hossein
Dalla Valle, Luisa
Van Doan, Hien
Carnevali, Oliana
A zebrafish HCT116 xenograft model to predict anandamide outcomes on colorectal cancer
title A zebrafish HCT116 xenograft model to predict anandamide outcomes on colorectal cancer
title_full A zebrafish HCT116 xenograft model to predict anandamide outcomes on colorectal cancer
title_fullStr A zebrafish HCT116 xenograft model to predict anandamide outcomes on colorectal cancer
title_full_unstemmed A zebrafish HCT116 xenograft model to predict anandamide outcomes on colorectal cancer
title_short A zebrafish HCT116 xenograft model to predict anandamide outcomes on colorectal cancer
title_sort zebrafish hct116 xenograft model to predict anandamide outcomes on colorectal cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789132/
https://www.ncbi.nlm.nih.gov/pubmed/36564370
http://dx.doi.org/10.1038/s41419-022-05523-z
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