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Growth of human digestive-tumour xenografts in athymic nude rats.

The athymic nude rat rnu/rnu has been established as an in vivo model for the acceptance of human digestive-tumour xenografts. We report the successful xenografting of 7/12 (58%) primary explants from patients with digestive cancer. Successful xenografting also occurred in 21/25 (84%) pancreatic tum...

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Autores principales: Davies, G., Duke, D., Grant, A. G., Kelly, S. A., Hermon-Taylor, J.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1981
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010503/
https://www.ncbi.nlm.nih.gov/pubmed/7459238
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author Davies, G.
Duke, D.
Grant, A. G.
Kelly, S. A.
Hermon-Taylor, J.
author_facet Davies, G.
Duke, D.
Grant, A. G.
Kelly, S. A.
Hermon-Taylor, J.
author_sort Davies, G.
collection PubMed
description The athymic nude rat rnu/rnu has been established as an in vivo model for the acceptance of human digestive-tumour xenografts. We report the successful xenografting of 7/12 (58%) primary explants from patients with digestive cancer. Successful xenografting also occurred in 21/25 (84%) pancreatic tumours derived from a pancreatic exocrine adenocarcinoma (GER) maintained in cell culture; 2 of those have been successfully passaged in nude rats. The simultaneous implantation of these tumours into nude mice led to an almost identical take rate. Passage of one colonic and one pancreatic xenograft from nude rats into nude mice, and transplantation back into nude rats, increased the take rates. The critical period for the establishment of primary tumour growth was usually 28-42 days. The xenografts maintained histological and cytological characteristics of the primary explants or of the original tumour from which the cell line derived. The karyotype of the cell line was also maintained in the solid tumour. Three murine tumours were successfully grown as xenografts. Despite their immunoincompetence, the rats in this study showed no increased morbidity or mortality when kept in conventional conditions, compared with animals housed in isolators. The athymic nude rat will become a valuable complementary tool to the nude mouse for the establishment and maintenance of human digestive tumours and for surgical and serial serological studies. IMAGES:
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spelling pubmed-20105032009-09-10 Growth of human digestive-tumour xenografts in athymic nude rats. Davies, G. Duke, D. Grant, A. G. Kelly, S. A. Hermon-Taylor, J. Br J Cancer Research Article The athymic nude rat rnu/rnu has been established as an in vivo model for the acceptance of human digestive-tumour xenografts. We report the successful xenografting of 7/12 (58%) primary explants from patients with digestive cancer. Successful xenografting also occurred in 21/25 (84%) pancreatic tumours derived from a pancreatic exocrine adenocarcinoma (GER) maintained in cell culture; 2 of those have been successfully passaged in nude rats. The simultaneous implantation of these tumours into nude mice led to an almost identical take rate. Passage of one colonic and one pancreatic xenograft from nude rats into nude mice, and transplantation back into nude rats, increased the take rates. The critical period for the establishment of primary tumour growth was usually 28-42 days. The xenografts maintained histological and cytological characteristics of the primary explants or of the original tumour from which the cell line derived. The karyotype of the cell line was also maintained in the solid tumour. Three murine tumours were successfully grown as xenografts. Despite their immunoincompetence, the rats in this study showed no increased morbidity or mortality when kept in conventional conditions, compared with animals housed in isolators. The athymic nude rat will become a valuable complementary tool to the nude mouse for the establishment and maintenance of human digestive tumours and for surgical and serial serological studies. IMAGES: Nature Publishing Group 1981-01 /pmc/articles/PMC2010503/ /pubmed/7459238 Text en https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Davies, G.
Duke, D.
Grant, A. G.
Kelly, S. A.
Hermon-Taylor, J.
Growth of human digestive-tumour xenografts in athymic nude rats.
title Growth of human digestive-tumour xenografts in athymic nude rats.
title_full Growth of human digestive-tumour xenografts in athymic nude rats.
title_fullStr Growth of human digestive-tumour xenografts in athymic nude rats.
title_full_unstemmed Growth of human digestive-tumour xenografts in athymic nude rats.
title_short Growth of human digestive-tumour xenografts in athymic nude rats.
title_sort growth of human digestive-tumour xenografts in athymic nude rats.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010503/
https://www.ncbi.nlm.nih.gov/pubmed/7459238
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