Cargando…
The human tumour cloning assay in the management of breast cancer patients.
A tumour cloning system was used to cultivate breast cancer specimens. Fifty-six percent of 87 samples were adequate for evaluation, showing clonal growth in about one third (35%). Effusions yielded significantly better growth than solid specimens, the median colony numbers being 64 and 18 respectiv...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1985
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977099/ https://www.ncbi.nlm.nih.gov/pubmed/4027163 |
_version_ | 1782135190371434496 |
---|---|
author | Dittrich, C. Jakesz, R. Wrba, F. Havelec, L. Haas, O. Spona, J. Holzner, H. Kolb, R. Moser, K. |
author_facet | Dittrich, C. Jakesz, R. Wrba, F. Havelec, L. Haas, O. Spona, J. Holzner, H. Kolb, R. Moser, K. |
author_sort | Dittrich, C. |
collection | PubMed |
description | A tumour cloning system was used to cultivate breast cancer specimens. Fifty-six percent of 87 samples were adequate for evaluation, showing clonal growth in about one third (35%). Effusions yielded significantly better growth than solid specimens, the median colony numbers being 64 and 18 respectively. An attempt was made to examine whether there was any association between parameters accepted as prognostic factors for breast cancer and clonal growth in vitro. No correlation was found between preoperative tumour burden, histopathologic grading, menopausal status or overall survival and clonal growth in vitro, whereas we observed an inverse trend between progesterone receptor content of the tumours and their growth potential (P less than 0.01). In those few cases where in vitro and in vivo data could be compared, a high accuracy of the predicted sensitivities was found with respect to chemotherapy, but not in relation to hormonal treatment. A statistically significant higher overall chemosensitivity was associated with the absence of oestrogen receptors (P less than 0.01). |
format | Text |
id | pubmed-1977099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1985 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19770992009-09-10 The human tumour cloning assay in the management of breast cancer patients. Dittrich, C. Jakesz, R. Wrba, F. Havelec, L. Haas, O. Spona, J. Holzner, H. Kolb, R. Moser, K. Br J Cancer Research Article A tumour cloning system was used to cultivate breast cancer specimens. Fifty-six percent of 87 samples were adequate for evaluation, showing clonal growth in about one third (35%). Effusions yielded significantly better growth than solid specimens, the median colony numbers being 64 and 18 respectively. An attempt was made to examine whether there was any association between parameters accepted as prognostic factors for breast cancer and clonal growth in vitro. No correlation was found between preoperative tumour burden, histopathologic grading, menopausal status or overall survival and clonal growth in vitro, whereas we observed an inverse trend between progesterone receptor content of the tumours and their growth potential (P less than 0.01). In those few cases where in vitro and in vivo data could be compared, a high accuracy of the predicted sensitivities was found with respect to chemotherapy, but not in relation to hormonal treatment. A statistically significant higher overall chemosensitivity was associated with the absence of oestrogen receptors (P less than 0.01). Nature Publishing Group 1985-08 /pmc/articles/PMC1977099/ /pubmed/4027163 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 Dittrich, C. Jakesz, R. Wrba, F. Havelec, L. Haas, O. Spona, J. Holzner, H. Kolb, R. Moser, K. The human tumour cloning assay in the management of breast cancer patients. |
title | The human tumour cloning assay in the management of breast cancer patients. |
title_full | The human tumour cloning assay in the management of breast cancer patients. |
title_fullStr | The human tumour cloning assay in the management of breast cancer patients. |
title_full_unstemmed | The human tumour cloning assay in the management of breast cancer patients. |
title_short | The human tumour cloning assay in the management of breast cancer patients. |
title_sort | human tumour cloning assay in the management of breast cancer patients. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977099/ https://www.ncbi.nlm.nih.gov/pubmed/4027163 |
work_keys_str_mv | AT dittrichc thehumantumourcloningassayinthemanagementofbreastcancerpatients AT jakeszr thehumantumourcloningassayinthemanagementofbreastcancerpatients AT wrbaf thehumantumourcloningassayinthemanagementofbreastcancerpatients AT havelecl thehumantumourcloningassayinthemanagementofbreastcancerpatients AT haaso thehumantumourcloningassayinthemanagementofbreastcancerpatients AT sponaj thehumantumourcloningassayinthemanagementofbreastcancerpatients AT holznerh thehumantumourcloningassayinthemanagementofbreastcancerpatients AT kolbr thehumantumourcloningassayinthemanagementofbreastcancerpatients AT moserk thehumantumourcloningassayinthemanagementofbreastcancerpatients AT dittrichc humantumourcloningassayinthemanagementofbreastcancerpatients AT jakeszr humantumourcloningassayinthemanagementofbreastcancerpatients AT wrbaf humantumourcloningassayinthemanagementofbreastcancerpatients AT havelecl humantumourcloningassayinthemanagementofbreastcancerpatients AT haaso humantumourcloningassayinthemanagementofbreastcancerpatients AT sponaj humantumourcloningassayinthemanagementofbreastcancerpatients AT holznerh humantumourcloningassayinthemanagementofbreastcancerpatients AT kolbr humantumourcloningassayinthemanagementofbreastcancerpatients AT moserk humantumourcloningassayinthemanagementofbreastcancerpatients |