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Differences in the expression of mucus-associated antigens between proximal and distal human colon adenocarcinomas.

An immunohistological study showed differences in the expression of mucus-associated gastric M1 and intestinal M3 antigens between the proximal (100 cases) and distal (200 cases) colonic adenocarcinomas. Such a regional difference was not observed in the normal colon. A total of 55% and 78% of proxi...

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Autores principales: Bara, J., Nardelli, J., Gadenne, C., Prade, M., Burtin, P.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1984
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976769/
https://www.ncbi.nlm.nih.gov/pubmed/6324842
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author Bara, J.
Nardelli, J.
Gadenne, C.
Prade, M.
Burtin, P.
author_facet Bara, J.
Nardelli, J.
Gadenne, C.
Prade, M.
Burtin, P.
author_sort Bara, J.
collection PubMed
description An immunohistological study showed differences in the expression of mucus-associated gastric M1 and intestinal M3 antigens between the proximal (100 cases) and distal (200 cases) colonic adenocarcinomas. Such a regional difference was not observed in the normal colon. A total of 55% and 78% of proximal tumours produced M1 and M3 antigens, respectively (versus 13% and 47% in the distal tumours). The high percentage of M1 positive proximal cancers could be explained by the higher percentage (i) of mucus-producing tumours, such as signet ring cell (6% vs 1%) or mucinous adenocarcinomas (29% vs 11%); and (ii) of M1(+) well-differentiated adenocarcinomas (45% vs 8.5%) and the presence of undifferentiated carcinoma producing M1 antigens (12% vs 0%). These latter carcinomas were found in older patients (mean age 78 years vs 66 years). These results suggest that, on the proximal side, the stem cells were more often engaged in a differentiation process involving the expression of M antigens than were those of the distal side. Moreover, the proximal stem cells more frequently produce a foetal differentiation program showing simultaneous expression of M3 and M1 antigens (in 48% of proximal tumours, vs 11.5% for the distal side). Around 12% of proximal adenocarcinomas (vs 2% of distal tumours) contained stem cells engaged in a cell differentiation program not observed in the normal adult or foetal colon, involving the predominant expression of M1 antigens associated with an undifferential histological pattern. IMAGES:
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spelling pubmed-19767692009-09-10 Differences in the expression of mucus-associated antigens between proximal and distal human colon adenocarcinomas. Bara, J. Nardelli, J. Gadenne, C. Prade, M. Burtin, P. Br J Cancer Research Article An immunohistological study showed differences in the expression of mucus-associated gastric M1 and intestinal M3 antigens between the proximal (100 cases) and distal (200 cases) colonic adenocarcinomas. Such a regional difference was not observed in the normal colon. A total of 55% and 78% of proximal tumours produced M1 and M3 antigens, respectively (versus 13% and 47% in the distal tumours). The high percentage of M1 positive proximal cancers could be explained by the higher percentage (i) of mucus-producing tumours, such as signet ring cell (6% vs 1%) or mucinous adenocarcinomas (29% vs 11%); and (ii) of M1(+) well-differentiated adenocarcinomas (45% vs 8.5%) and the presence of undifferentiated carcinoma producing M1 antigens (12% vs 0%). These latter carcinomas were found in older patients (mean age 78 years vs 66 years). These results suggest that, on the proximal side, the stem cells were more often engaged in a differentiation process involving the expression of M antigens than were those of the distal side. Moreover, the proximal stem cells more frequently produce a foetal differentiation program showing simultaneous expression of M3 and M1 antigens (in 48% of proximal tumours, vs 11.5% for the distal side). Around 12% of proximal adenocarcinomas (vs 2% of distal tumours) contained stem cells engaged in a cell differentiation program not observed in the normal adult or foetal colon, involving the predominant expression of M1 antigens associated with an undifferential histological pattern. IMAGES: Nature Publishing Group 1984-04 /pmc/articles/PMC1976769/ /pubmed/6324842 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
Bara, J.
Nardelli, J.
Gadenne, C.
Prade, M.
Burtin, P.
Differences in the expression of mucus-associated antigens between proximal and distal human colon adenocarcinomas.
title Differences in the expression of mucus-associated antigens between proximal and distal human colon adenocarcinomas.
title_full Differences in the expression of mucus-associated antigens between proximal and distal human colon adenocarcinomas.
title_fullStr Differences in the expression of mucus-associated antigens between proximal and distal human colon adenocarcinomas.
title_full_unstemmed Differences in the expression of mucus-associated antigens between proximal and distal human colon adenocarcinomas.
title_short Differences in the expression of mucus-associated antigens between proximal and distal human colon adenocarcinomas.
title_sort differences in the expression of mucus-associated antigens between proximal and distal human colon adenocarcinomas.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976769/
https://www.ncbi.nlm.nih.gov/pubmed/6324842
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