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A critical appraisal of the immunohistochemical detection of the c-myc oncogene product in colorectal cancer.

Expression of c-myc was studied immunohistochemically in 100 colorectal carcinomas, using a monoclonal antibody, Myc 1-6E10, which is purported to recognize the oncoprotein (p62c-myc) in paraffin-embedded material. In normal epithelium, maturing crypt cells and terminally differentiated surface cell...

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Autores principales: Jones, D. J., Ghosh, A. K., Moore, M., Schofield, P. F.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1987
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2002390/
https://www.ncbi.nlm.nih.gov/pubmed/3325094
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author Jones, D. J.
Ghosh, A. K.
Moore, M.
Schofield, P. F.
author_facet Jones, D. J.
Ghosh, A. K.
Moore, M.
Schofield, P. F.
author_sort Jones, D. J.
collection PubMed
description Expression of c-myc was studied immunohistochemically in 100 colorectal carcinomas, using a monoclonal antibody, Myc 1-6E10, which is purported to recognize the oncoprotein (p62c-myc) in paraffin-embedded material. In normal epithelium, maturing crypt cells and terminally differentiated surface cells were positive, and proliferating basal crypt cells negative. All carcinomas stained positively, but intensity was independent of histological differentiation, Dukes' stage, DNA ploidy and survival. Staining was predominantly cytoplasmic despite the suspected nuclear location of p62c-myc and there was considerable staining of fibroblasts. When staining was compared in frozen and paraffin-embedded sections fixed in different ways, different patterns were observed. Acetone-fixed frozen sections exhibited weak nuclear and cytoplasmic staining or were negative. In formol-saline fixed frozen sections, there was stronger predominantly nuclear staining. In paraffin-embedded sections staining was predominantly cytoplasmic. This study suggests that c-myc expression is enhanced in the majority of colorectal carcinomas and although independent of clinical behaviour, may be a common event in malignant transformation. However, since staining is affected by fixation and processing, data obtained using Myc 1-6E10 on routinely processed specimens should be interpreted with caution. IMAGES:
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spelling pubmed-20023902009-09-10 A critical appraisal of the immunohistochemical detection of the c-myc oncogene product in colorectal cancer. Jones, D. J. Ghosh, A. K. Moore, M. Schofield, P. F. Br J Cancer Research Article Expression of c-myc was studied immunohistochemically in 100 colorectal carcinomas, using a monoclonal antibody, Myc 1-6E10, which is purported to recognize the oncoprotein (p62c-myc) in paraffin-embedded material. In normal epithelium, maturing crypt cells and terminally differentiated surface cells were positive, and proliferating basal crypt cells negative. All carcinomas stained positively, but intensity was independent of histological differentiation, Dukes' stage, DNA ploidy and survival. Staining was predominantly cytoplasmic despite the suspected nuclear location of p62c-myc and there was considerable staining of fibroblasts. When staining was compared in frozen and paraffin-embedded sections fixed in different ways, different patterns were observed. Acetone-fixed frozen sections exhibited weak nuclear and cytoplasmic staining or were negative. In formol-saline fixed frozen sections, there was stronger predominantly nuclear staining. In paraffin-embedded sections staining was predominantly cytoplasmic. This study suggests that c-myc expression is enhanced in the majority of colorectal carcinomas and although independent of clinical behaviour, may be a common event in malignant transformation. However, since staining is affected by fixation and processing, data obtained using Myc 1-6E10 on routinely processed specimens should be interpreted with caution. IMAGES: Nature Publishing Group 1987-12 /pmc/articles/PMC2002390/ /pubmed/3325094 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
Jones, D. J.
Ghosh, A. K.
Moore, M.
Schofield, P. F.
A critical appraisal of the immunohistochemical detection of the c-myc oncogene product in colorectal cancer.
title A critical appraisal of the immunohistochemical detection of the c-myc oncogene product in colorectal cancer.
title_full A critical appraisal of the immunohistochemical detection of the c-myc oncogene product in colorectal cancer.
title_fullStr A critical appraisal of the immunohistochemical detection of the c-myc oncogene product in colorectal cancer.
title_full_unstemmed A critical appraisal of the immunohistochemical detection of the c-myc oncogene product in colorectal cancer.
title_short A critical appraisal of the immunohistochemical detection of the c-myc oncogene product in colorectal cancer.
title_sort critical appraisal of the immunohistochemical detection of the c-myc oncogene product in colorectal cancer.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2002390/
https://www.ncbi.nlm.nih.gov/pubmed/3325094
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