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Time course of ovarian tumour growth in soft agar culture.

Single time point assessment is usually employed in the Human Tumour Cloning System as the only parameter for in vitro growth. This does not seem to give a fair expression of the dynamic biological properties of tumour growth and time dependent effects, e.g. of cytotoxic drugs. We studied the time c...

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Autores principales: Verheijen, R. H., Feitz, W. F., Kenemans, P., Vooys, G. P., Herman, C. J.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1985
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977227/
https://www.ncbi.nlm.nih.gov/pubmed/4063146
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author Verheijen, R. H.
Feitz, W. F.
Kenemans, P.
Vooys, G. P.
Herman, C. J.
author_facet Verheijen, R. H.
Feitz, W. F.
Kenemans, P.
Vooys, G. P.
Herman, C. J.
author_sort Verheijen, R. H.
collection PubMed
description Single time point assessment is usually employed in the Human Tumour Cloning System as the only parameter for in vitro growth. This does not seem to give a fair expression of the dynamic biological properties of tumour growth and time dependent effects, e.g. of cytotoxic drugs. We studied the time course of colony formation in temporal growth patterns (TGPs) and compared this method of growth evaluation with conventional single time point assessment in 57 samples of ovarian tumour cultures in the HTCS. A first advantage of the use of TGPs is that more cultures become evaluable, as this assessment over time can detect a rise in the number of colonies in dishes where colony-like clumps have initially been seeded. Thus only 28 of the cultures were evaluable for single time point assessment, whereas 57 were available for TGP evaluation. Growth was more often seen at TGP evaluation (14/57) than at single day assessment (8/57). Evaluation of growth over the course of time potentially allows detection of sensitivity to drugs. Furthermore TGPs reflect the dynamics of biological growth. These features cannot be studied in single time point assessment.
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spelling pubmed-19772272009-09-10 Time course of ovarian tumour growth in soft agar culture. Verheijen, R. H. Feitz, W. F. Kenemans, P. Vooys, G. P. Herman, C. J. Br J Cancer Research Article Single time point assessment is usually employed in the Human Tumour Cloning System as the only parameter for in vitro growth. This does not seem to give a fair expression of the dynamic biological properties of tumour growth and time dependent effects, e.g. of cytotoxic drugs. We studied the time course of colony formation in temporal growth patterns (TGPs) and compared this method of growth evaluation with conventional single time point assessment in 57 samples of ovarian tumour cultures in the HTCS. A first advantage of the use of TGPs is that more cultures become evaluable, as this assessment over time can detect a rise in the number of colonies in dishes where colony-like clumps have initially been seeded. Thus only 28 of the cultures were evaluable for single time point assessment, whereas 57 were available for TGP evaluation. Growth was more often seen at TGP evaluation (14/57) than at single day assessment (8/57). Evaluation of growth over the course of time potentially allows detection of sensitivity to drugs. Furthermore TGPs reflect the dynamics of biological growth. These features cannot be studied in single time point assessment. Nature Publishing Group 1985-11 /pmc/articles/PMC1977227/ /pubmed/4063146 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
Verheijen, R. H.
Feitz, W. F.
Kenemans, P.
Vooys, G. P.
Herman, C. J.
Time course of ovarian tumour growth in soft agar culture.
title Time course of ovarian tumour growth in soft agar culture.
title_full Time course of ovarian tumour growth in soft agar culture.
title_fullStr Time course of ovarian tumour growth in soft agar culture.
title_full_unstemmed Time course of ovarian tumour growth in soft agar culture.
title_short Time course of ovarian tumour growth in soft agar culture.
title_sort time course of ovarian tumour growth in soft agar culture.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977227/
https://www.ncbi.nlm.nih.gov/pubmed/4063146
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