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Expression of MUC1 mucins inversely correlated with post-surgical survival of renal cell carcinoma patients

Surgical specimens of the normal kidney and of renal cell carcinoma (RCC) tissues at different stages of progression and of various histological grades were examined for the expression of MUC1 mucins with sialylated carbohydrates (sialylated MUC1 mucins) using a monoclonal antibody MY.1E12. Immunohi...

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Autores principales: Fujita, K, Denda, K, Yamamoto, M, Matsumoto, T, Fujime, M, Irimura, T
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363005/
https://www.ncbi.nlm.nih.gov/pubmed/10390012
http://dx.doi.org/10.1038/sj.bjc.6690355
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author Fujita, K
Denda, K
Yamamoto, M
Matsumoto, T
Fujime, M
Irimura, T
author_facet Fujita, K
Denda, K
Yamamoto, M
Matsumoto, T
Fujime, M
Irimura, T
author_sort Fujita, K
collection PubMed
description Surgical specimens of the normal kidney and of renal cell carcinoma (RCC) tissues at different stages of progression and of various histological grades were examined for the expression of MUC1 mucins with sialylated carbohydrates (sialylated MUC1 mucins) using a monoclonal antibody MY.1E12. Immunohistochemical studies revealed that the binding sites for this antibody were localized to the apical side of the epithelial cells of the distal convoluted tubules, Henle's loops and collecting ducts. However, proximal convoluted tubules, where RCC is considered to originate, were not stained. This antibody also bound strongly to RCC at advanced stages of progression and at metastatic sites, and to RCC of histologically high grades (undifferentiated). The epitope, presumably sialylated MUC1 mucin, was detected not only along the surface of the cell membranes but also in the cytoplasm. The level of expression of sialylated MUC1 mucins was inversely correlated with the survival of the patients with RCC and the disease-free survival period after curative surgery. Western blot analysis demonstrated that the electrophoretic mobility of sialylated MUC1 mucins of RCC was greater than that from the normal kidney. It is suggested that high levels of expression of sialylated MUC1 mucins in certain human RCC populations correlate with the aggressiveness of the disease, such as the tendency to form metastasis. © 1999 Cancer Research Campaign
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spelling pubmed-23630052009-09-10 Expression of MUC1 mucins inversely correlated with post-surgical survival of renal cell carcinoma patients Fujita, K Denda, K Yamamoto, M Matsumoto, T Fujime, M Irimura, T Br J Cancer Regular Article Surgical specimens of the normal kidney and of renal cell carcinoma (RCC) tissues at different stages of progression and of various histological grades were examined for the expression of MUC1 mucins with sialylated carbohydrates (sialylated MUC1 mucins) using a monoclonal antibody MY.1E12. Immunohistochemical studies revealed that the binding sites for this antibody were localized to the apical side of the epithelial cells of the distal convoluted tubules, Henle's loops and collecting ducts. However, proximal convoluted tubules, where RCC is considered to originate, were not stained. This antibody also bound strongly to RCC at advanced stages of progression and at metastatic sites, and to RCC of histologically high grades (undifferentiated). The epitope, presumably sialylated MUC1 mucin, was detected not only along the surface of the cell membranes but also in the cytoplasm. The level of expression of sialylated MUC1 mucins was inversely correlated with the survival of the patients with RCC and the disease-free survival period after curative surgery. Western blot analysis demonstrated that the electrophoretic mobility of sialylated MUC1 mucins of RCC was greater than that from the normal kidney. It is suggested that high levels of expression of sialylated MUC1 mucins in certain human RCC populations correlate with the aggressiveness of the disease, such as the tendency to form metastasis. © 1999 Cancer Research Campaign Nature Publishing Group 1999-04 /pmc/articles/PMC2363005/ /pubmed/10390012 http://dx.doi.org/10.1038/sj.bjc.6690355 Text en Copyright © 1999 Cancer Research Campaign 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 Regular Article
Fujita, K
Denda, K
Yamamoto, M
Matsumoto, T
Fujime, M
Irimura, T
Expression of MUC1 mucins inversely correlated with post-surgical survival of renal cell carcinoma patients
title Expression of MUC1 mucins inversely correlated with post-surgical survival of renal cell carcinoma patients
title_full Expression of MUC1 mucins inversely correlated with post-surgical survival of renal cell carcinoma patients
title_fullStr Expression of MUC1 mucins inversely correlated with post-surgical survival of renal cell carcinoma patients
title_full_unstemmed Expression of MUC1 mucins inversely correlated with post-surgical survival of renal cell carcinoma patients
title_short Expression of MUC1 mucins inversely correlated with post-surgical survival of renal cell carcinoma patients
title_sort expression of muc1 mucins inversely correlated with post-surgical survival of renal cell carcinoma patients
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363005/
https://www.ncbi.nlm.nih.gov/pubmed/10390012
http://dx.doi.org/10.1038/sj.bjc.6690355
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