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Preferential growth of bloodborne cancer cells in colonic anastomoses.

Intracardiac injection, in hooded Lister rats, of syngeneic MC28 sarcoma cells never induced tumour growth in normal bowel. Tumour growth occurred at the site of a colonic anastomosis if surgery preceded tumour injection but not if it followed tumour injection, even by as little as 1 h. Maximum enha...

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Autores principales: Skipper, D., Jeffrey, M. J., Cooper, A. J., Taylor, I., Alexander, P.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246463/
https://www.ncbi.nlm.nih.gov/pubmed/3408643
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author Skipper, D.
Jeffrey, M. J.
Cooper, A. J.
Taylor, I.
Alexander, P.
author_facet Skipper, D.
Jeffrey, M. J.
Cooper, A. J.
Taylor, I.
Alexander, P.
author_sort Skipper, D.
collection PubMed
description Intracardiac injection, in hooded Lister rats, of syngeneic MC28 sarcoma cells never induced tumour growth in normal bowel. Tumour growth occurred at the site of a colonic anastomosis if surgery preceded tumour injection but not if it followed tumour injection, even by as little as 1 h. Maximum enhancement of tumour growth occurred when the healing process had progressed between 2 and 8 days, with a peak at 5 to 7 days. The enhancing effect was largely over by the time the healing had progressed 14 days. The syngeneic OES5 breast carcinoma also grew at colonic anastomoses when surgery preceded tumour injection by 5 days, but not in normal colon. The MC28 sarcoma also grew at ileal anastomoses but not in the normal ileum after intracardiac injection. By injecting radiolabelled sarcoma cells, an estimate of the probability of a single bloodborne tumour cell lodging at a colonic anastomosis and leading to a tumour deposit was calculated to be of the order of 1:43 whereas the probability of the cell lodging in normal colon and causing a deposit is less than 1:4 x 10(4). IMAGES:
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spelling pubmed-22464632009-09-10 Preferential growth of bloodborne cancer cells in colonic anastomoses. Skipper, D. Jeffrey, M. J. Cooper, A. J. Taylor, I. Alexander, P. Br J Cancer Research Article Intracardiac injection, in hooded Lister rats, of syngeneic MC28 sarcoma cells never induced tumour growth in normal bowel. Tumour growth occurred at the site of a colonic anastomosis if surgery preceded tumour injection but not if it followed tumour injection, even by as little as 1 h. Maximum enhancement of tumour growth occurred when the healing process had progressed between 2 and 8 days, with a peak at 5 to 7 days. The enhancing effect was largely over by the time the healing had progressed 14 days. The syngeneic OES5 breast carcinoma also grew at colonic anastomoses when surgery preceded tumour injection by 5 days, but not in normal colon. The MC28 sarcoma also grew at ileal anastomoses but not in the normal ileum after intracardiac injection. By injecting radiolabelled sarcoma cells, an estimate of the probability of a single bloodborne tumour cell lodging at a colonic anastomosis and leading to a tumour deposit was calculated to be of the order of 1:43 whereas the probability of the cell lodging in normal colon and causing a deposit is less than 1:4 x 10(4). IMAGES: Nature Publishing Group 1988-06 /pmc/articles/PMC2246463/ /pubmed/3408643 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
Skipper, D.
Jeffrey, M. J.
Cooper, A. J.
Taylor, I.
Alexander, P.
Preferential growth of bloodborne cancer cells in colonic anastomoses.
title Preferential growth of bloodborne cancer cells in colonic anastomoses.
title_full Preferential growth of bloodborne cancer cells in colonic anastomoses.
title_fullStr Preferential growth of bloodborne cancer cells in colonic anastomoses.
title_full_unstemmed Preferential growth of bloodborne cancer cells in colonic anastomoses.
title_short Preferential growth of bloodborne cancer cells in colonic anastomoses.
title_sort preferential growth of bloodborne cancer cells in colonic anastomoses.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246463/
https://www.ncbi.nlm.nih.gov/pubmed/3408643
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