Cargando…
Development of a new metastatic human breast carcinoma xenograft line.
Xenografts originated from human tumours offer the most appropriate research material for in vivo experimental research. However, primary human breast carcinomas are difficult to grow when transplanted in athymic mice: tumour take is less than 15%. Recently, we have achieved 60% tumour take by injec...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1998
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2149914/ https://www.ncbi.nlm.nih.gov/pubmed/9484817 |
_version_ | 1782144549558157312 |
---|---|
author | Mehta, R. R. Graves, J. M. Shilkaitis, A. Das Gupta, T. K. |
author_facet | Mehta, R. R. Graves, J. M. Shilkaitis, A. Das Gupta, T. K. |
author_sort | Mehta, R. R. |
collection | PubMed |
description | Xenografts originated from human tumours offer the most appropriate research material for in vivo experimental research. However, primary human breast carcinomas are difficult to grow when transplanted in athymic mice: tumour take is less than 15%. Recently, we have achieved 60% tumour take by injecting tumour cell suspensions mixed with Matrigel. Human breast xenografts originated from primary breast carcinoma also frequently show the potential to metastasize spontaneously. In the present study, we generated a human breast carcinoma xenograft line (UISO-BCA-NMT-18) that shows 100% tumorigenicity and 80-100% lung metastasis when transplanted s.c. in athymic mice. We have studied in detail the characteristics of the xenograft and the patient's tumour from which the xenograft line originated. Both the xenograft and the patient's tumour showed intense staining for mutant p53 nuclear protein, and high expression of U-PA, PAI and u-PAR. In vivo growth of the xenograft is stimulated by exogenous supplementation of oestrogen. This xenograft is continuously growing in mice and has shown 80-100% metastasis for the last three successive in vivo passages. This well-characterized, oestrogen-responsive, metastatic breast carcinoma xenograft line will provide excellent research material for metastasis-related research. IMAGES: |
format | Text |
id | pubmed-2149914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-21499142009-09-10 Development of a new metastatic human breast carcinoma xenograft line. Mehta, R. R. Graves, J. M. Shilkaitis, A. Das Gupta, T. K. Br J Cancer Research Article Xenografts originated from human tumours offer the most appropriate research material for in vivo experimental research. However, primary human breast carcinomas are difficult to grow when transplanted in athymic mice: tumour take is less than 15%. Recently, we have achieved 60% tumour take by injecting tumour cell suspensions mixed with Matrigel. Human breast xenografts originated from primary breast carcinoma also frequently show the potential to metastasize spontaneously. In the present study, we generated a human breast carcinoma xenograft line (UISO-BCA-NMT-18) that shows 100% tumorigenicity and 80-100% lung metastasis when transplanted s.c. in athymic mice. We have studied in detail the characteristics of the xenograft and the patient's tumour from which the xenograft line originated. Both the xenograft and the patient's tumour showed intense staining for mutant p53 nuclear protein, and high expression of U-PA, PAI and u-PAR. In vivo growth of the xenograft is stimulated by exogenous supplementation of oestrogen. This xenograft is continuously growing in mice and has shown 80-100% metastasis for the last three successive in vivo passages. This well-characterized, oestrogen-responsive, metastatic breast carcinoma xenograft line will provide excellent research material for metastasis-related research. IMAGES: Nature Publishing Group 1998-02 /pmc/articles/PMC2149914/ /pubmed/9484817 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 Mehta, R. R. Graves, J. M. Shilkaitis, A. Das Gupta, T. K. Development of a new metastatic human breast carcinoma xenograft line. |
title | Development of a new metastatic human breast carcinoma xenograft line. |
title_full | Development of a new metastatic human breast carcinoma xenograft line. |
title_fullStr | Development of a new metastatic human breast carcinoma xenograft line. |
title_full_unstemmed | Development of a new metastatic human breast carcinoma xenograft line. |
title_short | Development of a new metastatic human breast carcinoma xenograft line. |
title_sort | development of a new metastatic human breast carcinoma xenograft line. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2149914/ https://www.ncbi.nlm.nih.gov/pubmed/9484817 |
work_keys_str_mv | AT mehtarr developmentofanewmetastatichumanbreastcarcinomaxenograftline AT gravesjm developmentofanewmetastatichumanbreastcarcinomaxenograftline AT shilkaitisa developmentofanewmetastatichumanbreastcarcinomaxenograftline AT dasguptatk developmentofanewmetastatichumanbreastcarcinomaxenograftline |