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Alpha-methylacyl-coenzyme A racemase expression in neuroendocrine neoplasms of the stomach
The enzyme alpha-methylacyl-coenzyme A racemase plays an important role in the beta-oxidation of branched-chain fatty acid and its derivatives. It has been used to detect prostatic adenocarcinoma and high-grade intraepithelial neoplasia, and recently also as a marker for other neoplasms, including t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3421105/ https://www.ncbi.nlm.nih.gov/pubmed/22782380 http://dx.doi.org/10.1007/s00428-012-1272-5 |
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author | Annenkov, Alexey Nishikura, Ken Domori, Koji Ajioka, Yoichi |
author_facet | Annenkov, Alexey Nishikura, Ken Domori, Koji Ajioka, Yoichi |
author_sort | Annenkov, Alexey |
collection | PubMed |
description | The enzyme alpha-methylacyl-coenzyme A racemase plays an important role in the beta-oxidation of branched-chain fatty acid and its derivatives. It has been used to detect prostatic adenocarcinoma and high-grade intraepithelial neoplasia, and recently also as a marker for other neoplasms, including those of the genitourinary system, breast, upper and lower gastrointestinal tract and their precursor lesions. We assessed expression of alpha-methylacyl-coenzyme A racemase by immunohistochemistry in neuroendocrine tumours of the stomach to determine differences in the incidence and pattern of expression among different types of gastric neuroendocrine tumours. While none of the grade 1 neuroendocrine tumours were immunoreactive, 67 % of grade 2 neuroendocrine tumours and 90 % of neuroendocrine carcinomas were positive for alpha-methylacyl-coenzyme A racemase. Furthermore, an adenocarcinoma component was found in 72.5 % (37 of 51) of neuroendocrine carcinomas, whereas none of the grade 1 and 2 neuroendocrine tumours contained an adenocarcinoma component. In 83 % of neuroendocrine carcinomas, the adenocarcinoma component was positive for alpha-methylacyl-coenzyme A racemase, and both adenocarcinoma and neuroendocrine carcinoma components stained positively in 78 % of these cases. Our results indicate that alpha-methylacyl-coenzyme A racemase is a useful marker for distinguishing between grade 1 (negative) and grade 2 neuroendocrine tumours, and neuroendocrine carcinoma of the stomach (frequently positive). Different patterns of alpha-methylacyl-coenzyme A racemase expression between gastric neuroendocrine tumours and neuroendocrine carcinoma suggest that these might develop via different tumourigenic pathways. |
format | Online Article Text |
id | pubmed-3421105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-34211052012-08-24 Alpha-methylacyl-coenzyme A racemase expression in neuroendocrine neoplasms of the stomach Annenkov, Alexey Nishikura, Ken Domori, Koji Ajioka, Yoichi Virchows Arch Original Article The enzyme alpha-methylacyl-coenzyme A racemase plays an important role in the beta-oxidation of branched-chain fatty acid and its derivatives. It has been used to detect prostatic adenocarcinoma and high-grade intraepithelial neoplasia, and recently also as a marker for other neoplasms, including those of the genitourinary system, breast, upper and lower gastrointestinal tract and their precursor lesions. We assessed expression of alpha-methylacyl-coenzyme A racemase by immunohistochemistry in neuroendocrine tumours of the stomach to determine differences in the incidence and pattern of expression among different types of gastric neuroendocrine tumours. While none of the grade 1 neuroendocrine tumours were immunoreactive, 67 % of grade 2 neuroendocrine tumours and 90 % of neuroendocrine carcinomas were positive for alpha-methylacyl-coenzyme A racemase. Furthermore, an adenocarcinoma component was found in 72.5 % (37 of 51) of neuroendocrine carcinomas, whereas none of the grade 1 and 2 neuroendocrine tumours contained an adenocarcinoma component. In 83 % of neuroendocrine carcinomas, the adenocarcinoma component was positive for alpha-methylacyl-coenzyme A racemase, and both adenocarcinoma and neuroendocrine carcinoma components stained positively in 78 % of these cases. Our results indicate that alpha-methylacyl-coenzyme A racemase is a useful marker for distinguishing between grade 1 (negative) and grade 2 neuroendocrine tumours, and neuroendocrine carcinoma of the stomach (frequently positive). Different patterns of alpha-methylacyl-coenzyme A racemase expression between gastric neuroendocrine tumours and neuroendocrine carcinoma suggest that these might develop via different tumourigenic pathways. Springer-Verlag 2012-07-11 2012 /pmc/articles/PMC3421105/ /pubmed/22782380 http://dx.doi.org/10.1007/s00428-012-1272-5 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Annenkov, Alexey Nishikura, Ken Domori, Koji Ajioka, Yoichi Alpha-methylacyl-coenzyme A racemase expression in neuroendocrine neoplasms of the stomach |
title | Alpha-methylacyl-coenzyme A racemase expression in neuroendocrine neoplasms of the stomach |
title_full | Alpha-methylacyl-coenzyme A racemase expression in neuroendocrine neoplasms of the stomach |
title_fullStr | Alpha-methylacyl-coenzyme A racemase expression in neuroendocrine neoplasms of the stomach |
title_full_unstemmed | Alpha-methylacyl-coenzyme A racemase expression in neuroendocrine neoplasms of the stomach |
title_short | Alpha-methylacyl-coenzyme A racemase expression in neuroendocrine neoplasms of the stomach |
title_sort | alpha-methylacyl-coenzyme a racemase expression in neuroendocrine neoplasms of the stomach |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3421105/ https://www.ncbi.nlm.nih.gov/pubmed/22782380 http://dx.doi.org/10.1007/s00428-012-1272-5 |
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