Cargando…

Response and recovery kinetics of a solid tumour after irradiation.

The effects of local tumour radiation over the dose range 7.5-30 Gy on the growth and cell kinetics of rat hepatoma H-4-II-E have been investigated. A plot of growth delays against log surviving fraction was linear below a fraction of 0.03, but failed to extrapolate to the origin. Following a single...

Descripción completa

Detalles Bibliográficos
Autores principales: Rowley, R., Hopkins, H. A., Betsill, W. L., Ritenour, E. R., Looney, W. B.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1980
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010441/
https://www.ncbi.nlm.nih.gov/pubmed/7437290
_version_ 1782136322766405632
author Rowley, R.
Hopkins, H. A.
Betsill, W. L.
Ritenour, E. R.
Looney, W. B.
author_facet Rowley, R.
Hopkins, H. A.
Betsill, W. L.
Ritenour, E. R.
Looney, W. B.
author_sort Rowley, R.
collection PubMed
description The effects of local tumour radiation over the dose range 7.5-30 Gy on the growth and cell kinetics of rat hepatoma H-4-II-E have been investigated. A plot of growth delays against log surviving fraction was linear below a fraction of 0.03, but failed to extrapolate to the origin. Following a single dose of 15 Gy to the tumour, DNA-precursor incorporation, labelling and mitotic indices were depressed for 7 days. Tumour cellularity, measured as DNA/g tumour, was reduced and the rate of increase of total clonogenic cells slower than after complete tumour recovery. From Day 7 to Day 9 all indices of proliferation recovered to about control levels, clonogenic cell numbers increased more rapidly and tumour cellularity was restored. Repopulation of the tumour therefore appeared to take place mainly after Day 7. Incorporation of [3H]-TdR into tumour DNA reached twice the control values on Day 9. The rate of tumour growth accelerated after the initial decrease, and maximum tumour growth rate was also twice the control values on Day 13. Accelerated growth rates in irradiated tumours, above those of control tumours, occurred 10-16 days after treatment. The effectiveness of sequential therapy may therefore be improved if given during this period of of accelerated tumour growth. IMAGES:
format Text
id pubmed-2010441
institution National Center for Biotechnology Information
language English
publishDate 1980
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-20104412009-09-10 Response and recovery kinetics of a solid tumour after irradiation. Rowley, R. Hopkins, H. A. Betsill, W. L. Ritenour, E. R. Looney, W. B. Br J Cancer Research Article The effects of local tumour radiation over the dose range 7.5-30 Gy on the growth and cell kinetics of rat hepatoma H-4-II-E have been investigated. A plot of growth delays against log surviving fraction was linear below a fraction of 0.03, but failed to extrapolate to the origin. Following a single dose of 15 Gy to the tumour, DNA-precursor incorporation, labelling and mitotic indices were depressed for 7 days. Tumour cellularity, measured as DNA/g tumour, was reduced and the rate of increase of total clonogenic cells slower than after complete tumour recovery. From Day 7 to Day 9 all indices of proliferation recovered to about control levels, clonogenic cell numbers increased more rapidly and tumour cellularity was restored. Repopulation of the tumour therefore appeared to take place mainly after Day 7. Incorporation of [3H]-TdR into tumour DNA reached twice the control values on Day 9. The rate of tumour growth accelerated after the initial decrease, and maximum tumour growth rate was also twice the control values on Day 13. Accelerated growth rates in irradiated tumours, above those of control tumours, occurred 10-16 days after treatment. The effectiveness of sequential therapy may therefore be improved if given during this period of of accelerated tumour growth. IMAGES: Nature Publishing Group 1980-10 /pmc/articles/PMC2010441/ /pubmed/7437290 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
Rowley, R.
Hopkins, H. A.
Betsill, W. L.
Ritenour, E. R.
Looney, W. B.
Response and recovery kinetics of a solid tumour after irradiation.
title Response and recovery kinetics of a solid tumour after irradiation.
title_full Response and recovery kinetics of a solid tumour after irradiation.
title_fullStr Response and recovery kinetics of a solid tumour after irradiation.
title_full_unstemmed Response and recovery kinetics of a solid tumour after irradiation.
title_short Response and recovery kinetics of a solid tumour after irradiation.
title_sort response and recovery kinetics of a solid tumour after irradiation.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010441/
https://www.ncbi.nlm.nih.gov/pubmed/7437290
work_keys_str_mv AT rowleyr responseandrecoverykineticsofasolidtumourafterirradiation
AT hopkinsha responseandrecoverykineticsofasolidtumourafterirradiation
AT betsillwl responseandrecoverykineticsofasolidtumourafterirradiation
AT ritenourer responseandrecoverykineticsofasolidtumourafterirradiation
AT looneywb responseandrecoverykineticsofasolidtumourafterirradiation