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Zebrafish as a Model Organism for the Development of Drugs for Skin Cancer
Skin cancer, which includes melanoma and squamous cell carcinoma, represents the most common type of cutaneous malignancy worldwide, and its incidence is expected to rise in the near future. This condition derives from acquired genetic dysregulation of signaling pathways involved in the proliferatio...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536038/ https://www.ncbi.nlm.nih.gov/pubmed/28718799 http://dx.doi.org/10.3390/ijms18071550 |
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author | Bootorabi, Fatemeh Manouchehri, Hamed Changizi, Reza Barker, Harlan Palazzo, Elisabetta Saltari, Annalisa Parikka, Mataleena Pincelli, Carlo Aspatwar, Ashok |
author_facet | Bootorabi, Fatemeh Manouchehri, Hamed Changizi, Reza Barker, Harlan Palazzo, Elisabetta Saltari, Annalisa Parikka, Mataleena Pincelli, Carlo Aspatwar, Ashok |
author_sort | Bootorabi, Fatemeh |
collection | PubMed |
description | Skin cancer, which includes melanoma and squamous cell carcinoma, represents the most common type of cutaneous malignancy worldwide, and its incidence is expected to rise in the near future. This condition derives from acquired genetic dysregulation of signaling pathways involved in the proliferation and apoptosis of skin cells. The development of animal models has allowed a better understanding of these pathomechanisms, with the possibility of carrying out toxicological screening and drug development. In particular, the zebrafish (Danio rerio) has been established as one of the most important model organisms for cancer research. This model is particularly suitable for live cell imaging and high-throughput drug screening in a large-scale fashion. Thanks to the recent advances in genome editing, such as the clustered regularly-interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) methodologies, the mechanisms associated with cancer development and progression, as well as drug resistance can be investigated and comprehended. With these unique tools, the zebrafish represents a powerful platform for skin cancer research in the development of target therapies. Here, we will review the advantages of using the zebrafish model for drug discovery and toxicological and phenotypical screening. We will focus in detail on the most recent progress in the field of zebrafish model generation for the study of melanoma and squamous cell carcinoma (SCC), including cancer cell injection and transgenic animal development. Moreover, we will report the latest compounds and small molecules under investigation in melanoma zebrafish models. |
format | Online Article Text |
id | pubmed-5536038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-55360382017-08-04 Zebrafish as a Model Organism for the Development of Drugs for Skin Cancer Bootorabi, Fatemeh Manouchehri, Hamed Changizi, Reza Barker, Harlan Palazzo, Elisabetta Saltari, Annalisa Parikka, Mataleena Pincelli, Carlo Aspatwar, Ashok Int J Mol Sci Review Skin cancer, which includes melanoma and squamous cell carcinoma, represents the most common type of cutaneous malignancy worldwide, and its incidence is expected to rise in the near future. This condition derives from acquired genetic dysregulation of signaling pathways involved in the proliferation and apoptosis of skin cells. The development of animal models has allowed a better understanding of these pathomechanisms, with the possibility of carrying out toxicological screening and drug development. In particular, the zebrafish (Danio rerio) has been established as one of the most important model organisms for cancer research. This model is particularly suitable for live cell imaging and high-throughput drug screening in a large-scale fashion. Thanks to the recent advances in genome editing, such as the clustered regularly-interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) methodologies, the mechanisms associated with cancer development and progression, as well as drug resistance can be investigated and comprehended. With these unique tools, the zebrafish represents a powerful platform for skin cancer research in the development of target therapies. Here, we will review the advantages of using the zebrafish model for drug discovery and toxicological and phenotypical screening. We will focus in detail on the most recent progress in the field of zebrafish model generation for the study of melanoma and squamous cell carcinoma (SCC), including cancer cell injection and transgenic animal development. Moreover, we will report the latest compounds and small molecules under investigation in melanoma zebrafish models. MDPI 2017-07-18 /pmc/articles/PMC5536038/ /pubmed/28718799 http://dx.doi.org/10.3390/ijms18071550 Text en © 2017 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 | Review Bootorabi, Fatemeh Manouchehri, Hamed Changizi, Reza Barker, Harlan Palazzo, Elisabetta Saltari, Annalisa Parikka, Mataleena Pincelli, Carlo Aspatwar, Ashok Zebrafish as a Model Organism for the Development of Drugs for Skin Cancer |
title | Zebrafish as a Model Organism for the Development of Drugs for Skin Cancer |
title_full | Zebrafish as a Model Organism for the Development of Drugs for Skin Cancer |
title_fullStr | Zebrafish as a Model Organism for the Development of Drugs for Skin Cancer |
title_full_unstemmed | Zebrafish as a Model Organism for the Development of Drugs for Skin Cancer |
title_short | Zebrafish as a Model Organism for the Development of Drugs for Skin Cancer |
title_sort | zebrafish as a model organism for the development of drugs for skin cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536038/ https://www.ncbi.nlm.nih.gov/pubmed/28718799 http://dx.doi.org/10.3390/ijms18071550 |
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