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Diagnosis of pancreatic adenocarcinoma by polymerase chain reaction from pancreatic secretions.

As mutations at codon 12 of the Ki-ras oncogene have been shown to occur in 90% of pancreatic adenocarcinomas, a novel strategy for the detection of these mutations in pancreatic secretions obtained at routine endoscopies was developed. Ki-ras DNA was amplified and screened for the presence of mutat...

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Autores principales: Trümper, L. H., Bürger, B., von Bonin, F., Hintze, A., von Blohn, G., Pfreundschuh, M., Daus, H.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033495/
https://www.ncbi.nlm.nih.gov/pubmed/8054276
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author Trümper, L. H.
Bürger, B.
von Bonin, F.
Hintze, A.
von Blohn, G.
Pfreundschuh, M.
Daus, H.
author_facet Trümper, L. H.
Bürger, B.
von Bonin, F.
Hintze, A.
von Blohn, G.
Pfreundschuh, M.
Daus, H.
author_sort Trümper, L. H.
collection PubMed
description As mutations at codon 12 of the Ki-ras oncogene have been shown to occur in 90% of pancreatic adenocarcinomas, a novel strategy for the detection of these mutations in pancreatic secretions obtained at routine endoscopies was developed. Ki-ras DNA was amplified and screened for the presence of mutations at codon 12 with a combination of different rapid, non-radioactive molecular biology techniques. Examination of DNA from cell lines and paraffin-embedded tumour samples was used to establish and test the strategy employed. Pancreatic secretions from 27 patients were examined for the presence of Ki-ras mutations. Mutations at codon 12 were detected in 16/16 secretions from patients with histologically confirmed carcinoma and from one patient with carcinoma of the bile duct. In six patients a mutation identical to the one found in the pancreatic secretions was also demonstrated in paraffin-embedded fine-needle biopsy or surgical samples. Of the remaining ten patients (who had pancreatitis or cholelithiasis) mutations were not found in nine. Ki-ras codon 12 mutation was identified in one of these patients however, and mucous cell hyperplasia of pancreatic ducts was found upon histological examination. These findings establish Ki-ras polymerase chain reaction from pancreatic secretions as a valuable new diagnostic procedure for the demonstration of malignant cells, possibly at an early stage of the disease. IMAGES:
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spelling pubmed-20334952009-09-10 Diagnosis of pancreatic adenocarcinoma by polymerase chain reaction from pancreatic secretions. Trümper, L. H. Bürger, B. von Bonin, F. Hintze, A. von Blohn, G. Pfreundschuh, M. Daus, H. Br J Cancer Research Article As mutations at codon 12 of the Ki-ras oncogene have been shown to occur in 90% of pancreatic adenocarcinomas, a novel strategy for the detection of these mutations in pancreatic secretions obtained at routine endoscopies was developed. Ki-ras DNA was amplified and screened for the presence of mutations at codon 12 with a combination of different rapid, non-radioactive molecular biology techniques. Examination of DNA from cell lines and paraffin-embedded tumour samples was used to establish and test the strategy employed. Pancreatic secretions from 27 patients were examined for the presence of Ki-ras mutations. Mutations at codon 12 were detected in 16/16 secretions from patients with histologically confirmed carcinoma and from one patient with carcinoma of the bile duct. In six patients a mutation identical to the one found in the pancreatic secretions was also demonstrated in paraffin-embedded fine-needle biopsy or surgical samples. Of the remaining ten patients (who had pancreatitis or cholelithiasis) mutations were not found in nine. Ki-ras codon 12 mutation was identified in one of these patients however, and mucous cell hyperplasia of pancreatic ducts was found upon histological examination. These findings establish Ki-ras polymerase chain reaction from pancreatic secretions as a valuable new diagnostic procedure for the demonstration of malignant cells, possibly at an early stage of the disease. IMAGES: Nature Publishing Group 1994-08 /pmc/articles/PMC2033495/ /pubmed/8054276 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
Trümper, L. H.
Bürger, B.
von Bonin, F.
Hintze, A.
von Blohn, G.
Pfreundschuh, M.
Daus, H.
Diagnosis of pancreatic adenocarcinoma by polymerase chain reaction from pancreatic secretions.
title Diagnosis of pancreatic adenocarcinoma by polymerase chain reaction from pancreatic secretions.
title_full Diagnosis of pancreatic adenocarcinoma by polymerase chain reaction from pancreatic secretions.
title_fullStr Diagnosis of pancreatic adenocarcinoma by polymerase chain reaction from pancreatic secretions.
title_full_unstemmed Diagnosis of pancreatic adenocarcinoma by polymerase chain reaction from pancreatic secretions.
title_short Diagnosis of pancreatic adenocarcinoma by polymerase chain reaction from pancreatic secretions.
title_sort diagnosis of pancreatic adenocarcinoma by polymerase chain reaction from pancreatic secretions.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033495/
https://www.ncbi.nlm.nih.gov/pubmed/8054276
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