Cargando…
Measurement of cell kinetics in cervical tumours using bromodeoxyuridine.
The pre-treatment cell kinetics of 120 cervical tumours were assessed following the in vivo labelling with the thymidine analogue Bromodeoxyuridine (BrdUrd). In 89% both static and temporal kinetic parameters could be measured. Through the analysis of multiple biopsies from each tumour marked intra...
Autores principales: | , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1993
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968308/ https://www.ncbi.nlm.nih.gov/pubmed/8318408 |
_version_ | 1782134711613652992 |
---|---|
author | Bolger, B. S. Cooke, T. G. Symonds, R. P. MacLean, A. B. Stanton, P. D. |
author_facet | Bolger, B. S. Cooke, T. G. Symonds, R. P. MacLean, A. B. Stanton, P. D. |
author_sort | Bolger, B. S. |
collection | PubMed |
description | The pre-treatment cell kinetics of 120 cervical tumours were assessed following the in vivo labelling with the thymidine analogue Bromodeoxyuridine (BrdUrd). In 89% both static and temporal kinetic parameters could be measured. Through the analysis of multiple biopsies from each tumour marked intra tumour heterogeneity was demonstrated. The median values for the most highly labelled sample analysed for each tumour were; S-phase duration (Ts) 12.1 h, BrdUrd labelling index (CLI) 9.5% and potential tumour doubling time 4.4 days. There was a significant elevation in CLI, but no difference in Ts, between tumour and non-neoplastic cervical tissue. There was a significant elevation in CLI, advanced stage and large size tumours. Although a significant elevation in CLI was found in aneuploid tumours this is likely to represent the systemic bias of the calculation methods, with no difference being seen between aneuploid and diploid tumours when BrdUrd labelling was measured with-out reference to the nuclei DNA content. The majority of these patients were treated with radiotherapy and cell kinetic data will be correlated with treatment response when adequate follow up has been achieved. |
format | Text |
id | pubmed-1968308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1993 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19683082009-09-10 Measurement of cell kinetics in cervical tumours using bromodeoxyuridine. Bolger, B. S. Cooke, T. G. Symonds, R. P. MacLean, A. B. Stanton, P. D. Br J Cancer Research Article The pre-treatment cell kinetics of 120 cervical tumours were assessed following the in vivo labelling with the thymidine analogue Bromodeoxyuridine (BrdUrd). In 89% both static and temporal kinetic parameters could be measured. Through the analysis of multiple biopsies from each tumour marked intra tumour heterogeneity was demonstrated. The median values for the most highly labelled sample analysed for each tumour were; S-phase duration (Ts) 12.1 h, BrdUrd labelling index (CLI) 9.5% and potential tumour doubling time 4.4 days. There was a significant elevation in CLI, but no difference in Ts, between tumour and non-neoplastic cervical tissue. There was a significant elevation in CLI, advanced stage and large size tumours. Although a significant elevation in CLI was found in aneuploid tumours this is likely to represent the systemic bias of the calculation methods, with no difference being seen between aneuploid and diploid tumours when BrdUrd labelling was measured with-out reference to the nuclei DNA content. The majority of these patients were treated with radiotherapy and cell kinetic data will be correlated with treatment response when adequate follow up has been achieved. Nature Publishing Group 1993-07 /pmc/articles/PMC1968308/ /pubmed/8318408 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 Bolger, B. S. Cooke, T. G. Symonds, R. P. MacLean, A. B. Stanton, P. D. Measurement of cell kinetics in cervical tumours using bromodeoxyuridine. |
title | Measurement of cell kinetics in cervical tumours using bromodeoxyuridine. |
title_full | Measurement of cell kinetics in cervical tumours using bromodeoxyuridine. |
title_fullStr | Measurement of cell kinetics in cervical tumours using bromodeoxyuridine. |
title_full_unstemmed | Measurement of cell kinetics in cervical tumours using bromodeoxyuridine. |
title_short | Measurement of cell kinetics in cervical tumours using bromodeoxyuridine. |
title_sort | measurement of cell kinetics in cervical tumours using bromodeoxyuridine. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968308/ https://www.ncbi.nlm.nih.gov/pubmed/8318408 |
work_keys_str_mv | AT bolgerbs measurementofcellkineticsincervicaltumoursusingbromodeoxyuridine AT cooketg measurementofcellkineticsincervicaltumoursusingbromodeoxyuridine AT symondsrp measurementofcellkineticsincervicaltumoursusingbromodeoxyuridine AT macleanab measurementofcellkineticsincervicaltumoursusingbromodeoxyuridine AT stantonpd measurementofcellkineticsincervicaltumoursusingbromodeoxyuridine |