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Quantitation of MHC antigen expression on colorectal tumours and its association with tumour progression.
A flow cytometric technique has been established for accurately quantitating the cell surface density of MHC antigens and the percentage of cells expressing MHC antigens in 38 colorectal tumours. Thirty-four percent of tumours were partially or completely negative for HLA-ABC antigen expression. Alt...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1987
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2001827/ https://www.ncbi.nlm.nih.gov/pubmed/3689659 |
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author | Durrant, L. G. Ballantyne, K. C. Armitage, N. C. Robins, R. A. Marksman, R. Hardcastle, J. D. Baldwin, R. W. |
author_facet | Durrant, L. G. Ballantyne, K. C. Armitage, N. C. Robins, R. A. Marksman, R. Hardcastle, J. D. Baldwin, R. W. |
author_sort | Durrant, L. G. |
collection | PubMed |
description | A flow cytometric technique has been established for accurately quantitating the cell surface density of MHC antigens and the percentage of cells expressing MHC antigens in 38 colorectal tumours. Thirty-four percent of tumours were partially or completely negative for HLA-ABC antigen expression. Although the quantity of HLA-ABC antigens varied widely, there was no correlation between the density of HLA-ABC antigens, or the percentage of cells expressing these antigens and clinicopathological stage. Fifty percent of the colorectal tumours expressed HLA-DR with varying antigen densities. All of the poorly differentiated tumours expressed HLA-DR but there was no correlation between expression of HLA-DR and clinicopathological stage. The aneuploid tumours expressed more HLA-ABC and HLA-DR antigens on a higher percentage of cells than the diploid tumours. Abnormal expression of the tumour associated antigens CEA, Y haptenic blood group and 791T p72 also correlated with expression of HLA-ABC and HLA-DR antigens on colorectal tumours. The majority of early derived in vitro dividing cells failed to express both HLA-ABC and HLA-DR antigens although they expressed high levels of tumour associated antigens. If there is a correlation between in vitro and in vivo growth perhaps tumours are maintained and seeded by MHC antigen negative cells. |
format | Text |
id | pubmed-2001827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1987 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20018272009-09-10 Quantitation of MHC antigen expression on colorectal tumours and its association with tumour progression. Durrant, L. G. Ballantyne, K. C. Armitage, N. C. Robins, R. A. Marksman, R. Hardcastle, J. D. Baldwin, R. W. Br J Cancer Research Article A flow cytometric technique has been established for accurately quantitating the cell surface density of MHC antigens and the percentage of cells expressing MHC antigens in 38 colorectal tumours. Thirty-four percent of tumours were partially or completely negative for HLA-ABC antigen expression. Although the quantity of HLA-ABC antigens varied widely, there was no correlation between the density of HLA-ABC antigens, or the percentage of cells expressing these antigens and clinicopathological stage. Fifty percent of the colorectal tumours expressed HLA-DR with varying antigen densities. All of the poorly differentiated tumours expressed HLA-DR but there was no correlation between expression of HLA-DR and clinicopathological stage. The aneuploid tumours expressed more HLA-ABC and HLA-DR antigens on a higher percentage of cells than the diploid tumours. Abnormal expression of the tumour associated antigens CEA, Y haptenic blood group and 791T p72 also correlated with expression of HLA-ABC and HLA-DR antigens on colorectal tumours. The majority of early derived in vitro dividing cells failed to express both HLA-ABC and HLA-DR antigens although they expressed high levels of tumour associated antigens. If there is a correlation between in vitro and in vivo growth perhaps tumours are maintained and seeded by MHC antigen negative cells. Nature Publishing Group 1987-10 /pmc/articles/PMC2001827/ /pubmed/3689659 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 Durrant, L. G. Ballantyne, K. C. Armitage, N. C. Robins, R. A. Marksman, R. Hardcastle, J. D. Baldwin, R. W. Quantitation of MHC antigen expression on colorectal tumours and its association with tumour progression. |
title | Quantitation of MHC antigen expression on colorectal tumours and its association with tumour progression. |
title_full | Quantitation of MHC antigen expression on colorectal tumours and its association with tumour progression. |
title_fullStr | Quantitation of MHC antigen expression on colorectal tumours and its association with tumour progression. |
title_full_unstemmed | Quantitation of MHC antigen expression on colorectal tumours and its association with tumour progression. |
title_short | Quantitation of MHC antigen expression on colorectal tumours and its association with tumour progression. |
title_sort | quantitation of mhc antigen expression on colorectal tumours and its association with tumour progression. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2001827/ https://www.ncbi.nlm.nih.gov/pubmed/3689659 |
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