Histological assessment of PAXgene tissue fixation and stabilization reagents.

Within SPIDIA, an EC FP7 project aimed to improve pre analytic procedures, the PAXgene Tissue System (PAXgene), was designed to improve tissue quality for parallel molecular and morphological analysis. Within the SPIDIA project promising results were found in both genomic and proteomic experiments w...

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Autores principales: Marcel Kap, Frank Smedts, Wolter Oosterhuis, Rosa Winther, Nanna Christensen, Bilge Reischauer, Christian Viertler, Daniel Groelz, Karl-Friedrich Becker, Kurt Zatloukal, Rupert Langer, Julia Slotta-Huspenina, Koppany Bodo, Bas de Jong, Uwe Oelmuller, Peter Riegman
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Publicado: Public Library of Science (PLoS) 2011
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spelling oai:doaj.org-article:75166d8670a14e3cb3e15d6db17fc7ce2021-11-18T07:34:07ZHistological assessment of PAXgene tissue fixation and stabilization reagents.1932-620310.1371/journal.pone.0027704https://doaj.org/article/75166d8670a14e3cb3e15d6db17fc7ce2011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22110732/?tool=EBIhttps://doaj.org/toc/1932-6203Within SPIDIA, an EC FP7 project aimed to improve pre analytic procedures, the PAXgene Tissue System (PAXgene), was designed to improve tissue quality for parallel molecular and morphological analysis. Within the SPIDIA project promising results were found in both genomic and proteomic experiments with PAXgene-fixed and paraffin embedded tissue derived biomolecules. But, for this technology to be accepted for use in both clinical and basic research, it is essential that its adequacy for preserving morphology and antigenicity is validated relative to formalin fixation. It is our aim to assess the suitability of PAXgene tissue fixation for (immuno)histological methods. Normal human tissue specimens (n = 70) were collected and divided into equal parts for fixation either with formalin or PAXgene. Sections of the obtained paraffin-embedded tissue were cut and stained. Morphological aspects of PAXgene-fixed tissue were described and also scored relative to formalin-fixed tissue. Performance of PAXgene-fixed tissue in immunohistochemical and in situ hybridization assays was also assessed relative to the corresponding formalin-fixed tissues. Morphology of PAXgene-fixed paraffin embedded tissue was well preserved and deemed adequate for diagnostics in most cases. Some antigens in PAXgene-fixed and paraffin embedded sections were detectable without the need for antigen retrieval, while others were detected using standard, formalin fixation based, immunohistochemistry protocols. Comparable results were obtained with in situ hybridization and histochemical stains. Basically all assessed histological techniques were found to be applicable to PAXgene-fixed and paraffin embedded tissue. In general results obtained with PAXgene-fixed tissue are comparable to those of formalin-fixed tissue. Compromises made in morphology can be called minor compared to the advantages in the molecular pathology possibilities.Marcel KapFrank SmedtsWolter OosterhuisRosa WintherNanna ChristensenBilge ReischauerChristian ViertlerDaniel GroelzKarl-Friedrich BeckerKurt ZatloukalRupert LangerJulia Slotta-HuspeninaKoppany BodoBas de JongUwe OelmullerPeter RiegmanPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 11, p e27704 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Marcel Kap
Frank Smedts
Wolter Oosterhuis
Rosa Winther
Nanna Christensen
Bilge Reischauer
Christian Viertler
Daniel Groelz
Karl-Friedrich Becker
Kurt Zatloukal
Rupert Langer
Julia Slotta-Huspenina
Koppany Bodo
Bas de Jong
Uwe Oelmuller
Peter Riegman
Histological assessment of PAXgene tissue fixation and stabilization reagents.
description Within SPIDIA, an EC FP7 project aimed to improve pre analytic procedures, the PAXgene Tissue System (PAXgene), was designed to improve tissue quality for parallel molecular and morphological analysis. Within the SPIDIA project promising results were found in both genomic and proteomic experiments with PAXgene-fixed and paraffin embedded tissue derived biomolecules. But, for this technology to be accepted for use in both clinical and basic research, it is essential that its adequacy for preserving morphology and antigenicity is validated relative to formalin fixation. It is our aim to assess the suitability of PAXgene tissue fixation for (immuno)histological methods. Normal human tissue specimens (n = 70) were collected and divided into equal parts for fixation either with formalin or PAXgene. Sections of the obtained paraffin-embedded tissue were cut and stained. Morphological aspects of PAXgene-fixed tissue were described and also scored relative to formalin-fixed tissue. Performance of PAXgene-fixed tissue in immunohistochemical and in situ hybridization assays was also assessed relative to the corresponding formalin-fixed tissues. Morphology of PAXgene-fixed paraffin embedded tissue was well preserved and deemed adequate for diagnostics in most cases. Some antigens in PAXgene-fixed and paraffin embedded sections were detectable without the need for antigen retrieval, while others were detected using standard, formalin fixation based, immunohistochemistry protocols. Comparable results were obtained with in situ hybridization and histochemical stains. Basically all assessed histological techniques were found to be applicable to PAXgene-fixed and paraffin embedded tissue. In general results obtained with PAXgene-fixed tissue are comparable to those of formalin-fixed tissue. Compromises made in morphology can be called minor compared to the advantages in the molecular pathology possibilities.
format article
author Marcel Kap
Frank Smedts
Wolter Oosterhuis
Rosa Winther
Nanna Christensen
Bilge Reischauer
Christian Viertler
Daniel Groelz
Karl-Friedrich Becker
Kurt Zatloukal
Rupert Langer
Julia Slotta-Huspenina
Koppany Bodo
Bas de Jong
Uwe Oelmuller
Peter Riegman
author_facet Marcel Kap
Frank Smedts
Wolter Oosterhuis
Rosa Winther
Nanna Christensen
Bilge Reischauer
Christian Viertler
Daniel Groelz
Karl-Friedrich Becker
Kurt Zatloukal
Rupert Langer
Julia Slotta-Huspenina
Koppany Bodo
Bas de Jong
Uwe Oelmuller
Peter Riegman
author_sort Marcel Kap
title Histological assessment of PAXgene tissue fixation and stabilization reagents.
title_short Histological assessment of PAXgene tissue fixation and stabilization reagents.
title_full Histological assessment of PAXgene tissue fixation and stabilization reagents.
title_fullStr Histological assessment of PAXgene tissue fixation and stabilization reagents.
title_full_unstemmed Histological assessment of PAXgene tissue fixation and stabilization reagents.
title_sort histological assessment of paxgene tissue fixation and stabilization reagents.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/75166d8670a14e3cb3e15d6db17fc7ce
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