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Preservation of biomolecules in breast cancer tissue by a formalin-free histology system
BACKGROUND: The potential problems associated with the use of formalin in histology, such as health hazards, degradation of RNA and cross-linking of proteins are well recognized. We describe the utilization of a formalin-free fixation and processing system for tissue detection of two important biopr...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267798/ https://www.ncbi.nlm.nih.gov/pubmed/18230182 http://dx.doi.org/10.1186/1472-6890-8-1 |
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author | Nassiri, Mehdi Ramos, Sharon Zohourian, Hajir Vincek, Vladimir Morales, Azorides R Nadji, Mehrdad |
author_facet | Nassiri, Mehdi Ramos, Sharon Zohourian, Hajir Vincek, Vladimir Morales, Azorides R Nadji, Mehrdad |
author_sort | Nassiri, Mehdi |
collection | PubMed |
description | BACKGROUND: The potential problems associated with the use of formalin in histology, such as health hazards, degradation of RNA and cross-linking of proteins are well recognized. We describe the utilization of a formalin-free fixation and processing system for tissue detection of two important biopredictors in breast cancer – estrogen receptor and HER2 – at the RNA and protein levels. METHODS: Parallel sections of 62 cases of breast cancer were fixed in an alcohol-based molecular fixative and in formalin. Molecular fixative samples were processed by a novel formalin-free microwave-assisted processing system that preserves DNA, RNA and proteins. Formalin-fixed samples were processed using the conventional method. Estrogen receptor was assessed by immunohistochemistry and real-time PCR. HER2 was assessed by immunohistochemistry, FISH, CISH and real-time PCR. RESULTS: The immunohistochemical reaction for estrogen receptor was similar in molecular- and formalin-fixed samples (Spearman Rank R = 0.83, p < 0.05). Also HER2 result was similar to that of formalin-fixed counterparts after elimination of antigen retrieval step (Spearman Rank R = 0.84, p < 0.05). The result of HER2 amplification by FISH and CISH was identical in the molecular fixative and formalin-fixed samples; although a shorter digestion step was required when using the former fixative. Real-time PCR for both estrogen receptor and HER2 were successful in all of the molecular fixative specimens. CONCLUSION: The formalin-free tissue fixation and processing system is a practical platform for evaluation of biomolecular markers in breast cancer and it allows reliable DNA and RNA and protein studies. |
format | Text |
id | pubmed-2267798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22677982008-03-15 Preservation of biomolecules in breast cancer tissue by a formalin-free histology system Nassiri, Mehdi Ramos, Sharon Zohourian, Hajir Vincek, Vladimir Morales, Azorides R Nadji, Mehrdad BMC Clin Pathol Research Article BACKGROUND: The potential problems associated with the use of formalin in histology, such as health hazards, degradation of RNA and cross-linking of proteins are well recognized. We describe the utilization of a formalin-free fixation and processing system for tissue detection of two important biopredictors in breast cancer – estrogen receptor and HER2 – at the RNA and protein levels. METHODS: Parallel sections of 62 cases of breast cancer were fixed in an alcohol-based molecular fixative and in formalin. Molecular fixative samples were processed by a novel formalin-free microwave-assisted processing system that preserves DNA, RNA and proteins. Formalin-fixed samples were processed using the conventional method. Estrogen receptor was assessed by immunohistochemistry and real-time PCR. HER2 was assessed by immunohistochemistry, FISH, CISH and real-time PCR. RESULTS: The immunohistochemical reaction for estrogen receptor was similar in molecular- and formalin-fixed samples (Spearman Rank R = 0.83, p < 0.05). Also HER2 result was similar to that of formalin-fixed counterparts after elimination of antigen retrieval step (Spearman Rank R = 0.84, p < 0.05). The result of HER2 amplification by FISH and CISH was identical in the molecular fixative and formalin-fixed samples; although a shorter digestion step was required when using the former fixative. Real-time PCR for both estrogen receptor and HER2 were successful in all of the molecular fixative specimens. CONCLUSION: The formalin-free tissue fixation and processing system is a practical platform for evaluation of biomolecular markers in breast cancer and it allows reliable DNA and RNA and protein studies. BioMed Central 2008-01-29 /pmc/articles/PMC2267798/ /pubmed/18230182 http://dx.doi.org/10.1186/1472-6890-8-1 Text en Copyright ©2008 Nassiri et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Nassiri, Mehdi Ramos, Sharon Zohourian, Hajir Vincek, Vladimir Morales, Azorides R Nadji, Mehrdad Preservation of biomolecules in breast cancer tissue by a formalin-free histology system |
title | Preservation of biomolecules in breast cancer tissue by a formalin-free histology system |
title_full | Preservation of biomolecules in breast cancer tissue by a formalin-free histology system |
title_fullStr | Preservation of biomolecules in breast cancer tissue by a formalin-free histology system |
title_full_unstemmed | Preservation of biomolecules in breast cancer tissue by a formalin-free histology system |
title_short | Preservation of biomolecules in breast cancer tissue by a formalin-free histology system |
title_sort | preservation of biomolecules in breast cancer tissue by a formalin-free histology system |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267798/ https://www.ncbi.nlm.nih.gov/pubmed/18230182 http://dx.doi.org/10.1186/1472-6890-8-1 |
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