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...

Descripción completa

Detalles Bibliográficos
Autores principales: Bolger, B. S., Cooke, T. G., Symonds, R. P., MacLean, A. B., Stanton, P. D.
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