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Clonogenic cell survival in cryopreserved human tumour cells.

Cells from 3 human tumours have been grown in soft agar contained in Millipore diffusion chambers and implanted i.p. in mice. Clonal growth was obtained from fresh biopsy samples, from cryopreserved tissue, and from xenografts of the tissues in immune-suppressed mice. The radiosensitivities of a mel...

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Detalles Bibliográficos
Autores principales: Selby, P. J., Steel, G. G.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1981
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010530/
https://www.ncbi.nlm.nih.gov/pubmed/7470378
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author Selby, P. J.
Steel, G. G.
author_facet Selby, P. J.
Steel, G. G.
author_sort Selby, P. J.
collection PubMed
description Cells from 3 human tumours have been grown in soft agar contained in Millipore diffusion chambers and implanted i.p. in mice. Clonal growth was obtained from fresh biopsy samples, from cryopreserved tissue, and from xenografts of the tissues in immune-suppressed mice. The radiosensitivities of a melanoma and an ovarian carcinoma were evaluated by in vitro irradiation before assay for colony formation. Xenografting did not modify the radiosensitivity of the melanoma. Cells from another tumour were exposed to Adriamycin or cyclophosphamide whilst contained within i.p. diffusion chambers; the sensitivity was similar for cryopreserved and xenografted cells. The results encourage further attempts to quantify the sensitivity of human tumour cells by these methods.
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spelling pubmed-20105302009-09-10 Clonogenic cell survival in cryopreserved human tumour cells. Selby, P. J. Steel, G. G. Br J Cancer Research Article Cells from 3 human tumours have been grown in soft agar contained in Millipore diffusion chambers and implanted i.p. in mice. Clonal growth was obtained from fresh biopsy samples, from cryopreserved tissue, and from xenografts of the tissues in immune-suppressed mice. The radiosensitivities of a melanoma and an ovarian carcinoma were evaluated by in vitro irradiation before assay for colony formation. Xenografting did not modify the radiosensitivity of the melanoma. Cells from another tumour were exposed to Adriamycin or cyclophosphamide whilst contained within i.p. diffusion chambers; the sensitivity was similar for cryopreserved and xenografted cells. The results encourage further attempts to quantify the sensitivity of human tumour cells by these methods. Nature Publishing Group 1981-02 /pmc/articles/PMC2010530/ /pubmed/7470378 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
Selby, P. J.
Steel, G. G.
Clonogenic cell survival in cryopreserved human tumour cells.
title Clonogenic cell survival in cryopreserved human tumour cells.
title_full Clonogenic cell survival in cryopreserved human tumour cells.
title_fullStr Clonogenic cell survival in cryopreserved human tumour cells.
title_full_unstemmed Clonogenic cell survival in cryopreserved human tumour cells.
title_short Clonogenic cell survival in cryopreserved human tumour cells.
title_sort clonogenic cell survival in cryopreserved human tumour cells.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010530/
https://www.ncbi.nlm.nih.gov/pubmed/7470378
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