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Systematic heterogeneity and prognostic significance of cell proliferation in colorectal cancer.
The prognosis of colorectal cancer has not significantly changed during the last 30 years. While evaluation of tumour cell proliferation may provide prognostic information, results obtained so far have been contradictory Heterogeneity in tumour cell proliferation may explain these contradictions. Wi...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1998
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150107/ https://www.ncbi.nlm.nih.gov/pubmed/9528835 |
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author | Palmqvist, R. Oberg, A. Bergström, C. Rutegård, J. N. Zackrisson, B. Stenling, R. |
author_facet | Palmqvist, R. Oberg, A. Bergström, C. Rutegård, J. N. Zackrisson, B. Stenling, R. |
author_sort | Palmqvist, R. |
collection | PubMed |
description | The prognosis of colorectal cancer has not significantly changed during the last 30 years. While evaluation of tumour cell proliferation may provide prognostic information, results obtained so far have been contradictory Heterogeneity in tumour cell proliferation may explain these contradictions. With in vivo injection of iododeoxyuridine (IdUrd), estimation of labelling index (LI), S-phase transit time (Ts) and potential doubling time (Tpot) may be performed from a single sample. A total of 109 colorectal cancers were studied after in vivo injection of IdUrd before surgical removal. From each cancer, four to eight samples were processed for both flow cytometrical (FCM) and immunohistochemical (IHC) visualization of IdUrd incorporation. LI/IHC was morphometrically quantified at both the luminal border and the invasive margin of these tumours. LI was significantly higher at the luminal border compared with the invasive margin, although they were correlated with each other. Using combined IHC and FCM methods, rapidly growing colorectal cancers (high LI and/or low Tpot) showed an increased survival (significant for LI at the invasive margin and for Tpot at both the invasive margin and the luminal border) in the entire unselected material and for radically removed Dukes' B tumours. FCM data alone did not discriminate for survival, with the exception of Ts in diploid and radically removed Dukes' B tumours. IMAGES: |
format | Text |
id | pubmed-2150107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-21501072009-09-10 Systematic heterogeneity and prognostic significance of cell proliferation in colorectal cancer. Palmqvist, R. Oberg, A. Bergström, C. RutegÃ¥rd, J. N. Zackrisson, B. Stenling, R. Br J Cancer Research Article The prognosis of colorectal cancer has not significantly changed during the last 30 years. While evaluation of tumour cell proliferation may provide prognostic information, results obtained so far have been contradictory Heterogeneity in tumour cell proliferation may explain these contradictions. With in vivo injection of iododeoxyuridine (IdUrd), estimation of labelling index (LI), S-phase transit time (Ts) and potential doubling time (Tpot) may be performed from a single sample. A total of 109 colorectal cancers were studied after in vivo injection of IdUrd before surgical removal. From each cancer, four to eight samples were processed for both flow cytometrical (FCM) and immunohistochemical (IHC) visualization of IdUrd incorporation. LI/IHC was morphometrically quantified at both the luminal border and the invasive margin of these tumours. LI was significantly higher at the luminal border compared with the invasive margin, although they were correlated with each other. Using combined IHC and FCM methods, rapidly growing colorectal cancers (high LI and/or low Tpot) showed an increased survival (significant for LI at the invasive margin and for Tpot at both the invasive margin and the luminal border) in the entire unselected material and for radically removed Dukes' B tumours. FCM data alone did not discriminate for survival, with the exception of Ts in diploid and radically removed Dukes' B tumours. IMAGES: Nature Publishing Group 1998-03 /pmc/articles/PMC2150107/ /pubmed/9528835 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 Palmqvist, R. Oberg, A. Bergström, C. Rutegård, J. N. Zackrisson, B. Stenling, R. Systematic heterogeneity and prognostic significance of cell proliferation in colorectal cancer. |
title | Systematic heterogeneity and prognostic significance of cell proliferation in colorectal cancer. |
title_full | Systematic heterogeneity and prognostic significance of cell proliferation in colorectal cancer. |
title_fullStr | Systematic heterogeneity and prognostic significance of cell proliferation in colorectal cancer. |
title_full_unstemmed | Systematic heterogeneity and prognostic significance of cell proliferation in colorectal cancer. |
title_short | Systematic heterogeneity and prognostic significance of cell proliferation in colorectal cancer. |
title_sort | systematic heterogeneity and prognostic significance of cell proliferation in colorectal cancer. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150107/ https://www.ncbi.nlm.nih.gov/pubmed/9528835 |
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