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dc.contributor.authorFrantz, William Tyler
dc.contributor.authorCeol, Craig J.
dc.date2022-08-11T08:09:56.000
dc.date.accessioned2022-08-23T16:49:26Z
dc.date.available2022-08-23T16:49:26Z
dc.date.issued2020-05-22
dc.date.submitted2020-06-05
dc.identifier.citation<p>Frantz WT, Ceol CJ. From Tank to Treatment: Modeling Melanoma in Zebrafish. Cells. 2020 May 22;9(5):E1289. doi: 10.3390/cells9051289. PMID: 32455885. <a href="https://doi.org/10.3390/cells9051289">Link to article on publisher's site</a></p>
dc.identifier.issn2073-4409 (Linking)
dc.identifier.doi10.3390/cells9051289
dc.identifier.pmid32455885
dc.identifier.urihttp://hdl.handle.net/20.500.14038/41460
dc.description.abstractMelanoma is the deadliest form of skin cancer and one of few cancers with a growing incidence. A thorough understanding of its pathogenesis is fundamental to developing new strategies to combat mortality and morbidity. Zebrafish-due in large part to their tractable genetics, conserved pathways, and optical properties-have emerged as an excellent system to model melanoma. Zebrafish have been used to study melanoma from a single tumor initiating cell, through metastasis, remission, and finally into relapse. In this review, we examine seminal zebrafish studies that have advanced our understanding of melanoma.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=32455885&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rights© 2020 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/).
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectMelanoma
dc.subjectgenetics
dc.subjectmelanocytes
dc.subjectmicroenvironment
dc.subjectmodeling
dc.subjectxenografts
dc.subjectzebrafish
dc.subjectAnimal Experimentation and Research
dc.subjectCancer Biology
dc.subjectDisease Modeling
dc.subjectGenetics and Genomics
dc.subjectMolecular Biology
dc.subjectNeoplasms
dc.titleFrom Tank to Treatment: Modeling Melanoma in Zebrafish
dc.typeJournal Article
dc.source.journaltitleCells
dc.source.volume9
dc.source.issue5
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=5258&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/4239
dc.identifier.contextkey17992629
refterms.dateFOA2022-08-23T16:49:26Z
html.description.abstract<p>Melanoma is the deadliest form of skin cancer and one of few cancers with a growing incidence. A thorough understanding of its pathogenesis is fundamental to developing new strategies to combat mortality and morbidity. Zebrafish-due in large part to their tractable genetics, conserved pathways, and optical properties-have emerged as an excellent system to model melanoma. Zebrafish have been used to study melanoma from a single tumor initiating cell, through metastasis, remission, and finally into relapse. In this review, we examine seminal zebrafish studies that have advanced our understanding of melanoma.</p>
dc.identifier.submissionpathoapubs/4239
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.contributor.departmentDepartment of Molecular, Cell, and Cancer Biology
dc.contributor.departmentProgram in Molecular Medicine


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© 2020 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/).
Except where otherwise noted, this item's license is described as © 2020 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/).