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Patched Knockout Mouse Models of Basal Cell Carcinoma

Basal cell carcinoma (BCC) is the most common human tumor. Mutations in the hedgehog (HH) receptor Patched (PTCH) are the main cause of BCC. Due to their high and increasing incidence, BCC are becoming all the more important for the health care system. Adequate animal models are required for the imp...

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Autores principales: Nitzki, Frauke, Becker, Marco, Frommhold, Anke, Schulz-Schaeffer, Walter, Hahn, Heidi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3449132/
https://www.ncbi.nlm.nih.gov/pubmed/23024864
http://dx.doi.org/10.1155/2012/907543
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author Nitzki, Frauke
Becker, Marco
Frommhold, Anke
Schulz-Schaeffer, Walter
Hahn, Heidi
author_facet Nitzki, Frauke
Becker, Marco
Frommhold, Anke
Schulz-Schaeffer, Walter
Hahn, Heidi
author_sort Nitzki, Frauke
collection PubMed
description Basal cell carcinoma (BCC) is the most common human tumor. Mutations in the hedgehog (HH) receptor Patched (PTCH) are the main cause of BCC. Due to their high and increasing incidence, BCC are becoming all the more important for the health care system. Adequate animal models are required for the improvement of current treatment strategies. A good model should reflect the situation in humans (i.e., BCC initiation due to Ptch mutations on an immunocompetent background) and should allow for (i) BCC induction at a defined time point, (ii) analysis of defined BCC stages, and (iii) induction of BCC in 100% of animals. In addition, it should be easy to handle. Here, we compare several currently existing conventional and conditional Ptch knockout mouse models for BCC and their potential use in preclinical research. In addition, we provide new data using conditional Ptch (flox/flox) mice and the K5-Cre-ER (T+/−) driver.
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spelling pubmed-34491322012-09-28 Patched Knockout Mouse Models of Basal Cell Carcinoma Nitzki, Frauke Becker, Marco Frommhold, Anke Schulz-Schaeffer, Walter Hahn, Heidi J Skin Cancer Review Article Basal cell carcinoma (BCC) is the most common human tumor. Mutations in the hedgehog (HH) receptor Patched (PTCH) are the main cause of BCC. Due to their high and increasing incidence, BCC are becoming all the more important for the health care system. Adequate animal models are required for the improvement of current treatment strategies. A good model should reflect the situation in humans (i.e., BCC initiation due to Ptch mutations on an immunocompetent background) and should allow for (i) BCC induction at a defined time point, (ii) analysis of defined BCC stages, and (iii) induction of BCC in 100% of animals. In addition, it should be easy to handle. Here, we compare several currently existing conventional and conditional Ptch knockout mouse models for BCC and their potential use in preclinical research. In addition, we provide new data using conditional Ptch (flox/flox) mice and the K5-Cre-ER (T+/−) driver. Hindawi Publishing Corporation 2012 2012-09-13 /pmc/articles/PMC3449132/ /pubmed/23024864 http://dx.doi.org/10.1155/2012/907543 Text en Copyright © 2012 Frauke Nitzki et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Nitzki, Frauke
Becker, Marco
Frommhold, Anke
Schulz-Schaeffer, Walter
Hahn, Heidi
Patched Knockout Mouse Models of Basal Cell Carcinoma
title Patched Knockout Mouse Models of Basal Cell Carcinoma
title_full Patched Knockout Mouse Models of Basal Cell Carcinoma
title_fullStr Patched Knockout Mouse Models of Basal Cell Carcinoma
title_full_unstemmed Patched Knockout Mouse Models of Basal Cell Carcinoma
title_short Patched Knockout Mouse Models of Basal Cell Carcinoma
title_sort patched knockout mouse models of basal cell carcinoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3449132/
https://www.ncbi.nlm.nih.gov/pubmed/23024864
http://dx.doi.org/10.1155/2012/907543
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