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A novel method for analyzing formalin-fixed paraffin embedded (FFPE) tissue sections by mass spectrometry imaging

Significant advances have been made in the past decade in the field of mass spectrometry imaging (MS imaging). It is a relatively unestablished technique aimed at direct, high-sensitive and spatially exclusive detection of biological molecules from the surface of tissue sections, so that semi-quanti...

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Autores principales: Aoki, Yutaka, Toyama, Atsuhiko, Shimada, Takashi, Sugita, Tetsuyoshi, Aoki, Chikage, Umino, Yukari, Suzuki, Atsushi, Aoki, Daisuke, Daigo, Yataro, Nakamura, Yusuke, Sato, Taka-Aki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859273/
https://www.ncbi.nlm.nih.gov/pubmed/24367147
http://dx.doi.org/10.2183/pjab/83.205
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author Aoki, Yutaka
Toyama, Atsuhiko
Shimada, Takashi
Sugita, Tetsuyoshi
Aoki, Chikage
Umino, Yukari
Suzuki, Atsushi
Aoki, Daisuke
Daigo, Yataro
Nakamura, Yusuke
Sato, Taka-Aki
author_facet Aoki, Yutaka
Toyama, Atsuhiko
Shimada, Takashi
Sugita, Tetsuyoshi
Aoki, Chikage
Umino, Yukari
Suzuki, Atsushi
Aoki, Daisuke
Daigo, Yataro
Nakamura, Yusuke
Sato, Taka-Aki
author_sort Aoki, Yutaka
collection PubMed
description Significant advances have been made in the past decade in the field of mass spectrometry imaging (MS imaging). It is a relatively unestablished technique aimed at direct, high-sensitive and spatially exclusive detection of biological molecules from the surface of tissue sections, so that semi-quantitative distribution map of the analyte can be reconstituted from the mass spectra obtained. There is tremendous potential in its application especially in clinical field, such as biomarker discovery or pharmacokinetic study. However, vast majority of the work has been performed on frozen tissue sections, while it remains generally unpractical to produce frozen sections with clinically resected tumor samples. Here we report our novel sample preparation technique that enabled MS imaging from formalin-fixed paraffin embedded (FFPE) tissue section, including retrospective archive as old as 11 years. FFPE sections were first dewaxed with pre-warmed xylene, and exposed tissue surface was enzymatically digested in nanoliter scale droplets to retain analyte localization. As a result, we succeeded in obtaining MS images of peptide peaks derived from several proteins, identified by MS/MS analysis, using ovarian cancer FFPE sections. The qualities of mass spectra obtained by this method were not significantly different from those obtained from frozen sections. By this, we opened the door to retrospective study of past clinical cases in aim to discover molecular biomarker.
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spelling pubmed-38592732013-12-23 A novel method for analyzing formalin-fixed paraffin embedded (FFPE) tissue sections by mass spectrometry imaging Aoki, Yutaka Toyama, Atsuhiko Shimada, Takashi Sugita, Tetsuyoshi Aoki, Chikage Umino, Yukari Suzuki, Atsushi Aoki, Daisuke Daigo, Yataro Nakamura, Yusuke Sato, Taka-Aki Proc Jpn Acad Ser B Phys Biol Sci Articles Significant advances have been made in the past decade in the field of mass spectrometry imaging (MS imaging). It is a relatively unestablished technique aimed at direct, high-sensitive and spatially exclusive detection of biological molecules from the surface of tissue sections, so that semi-quantitative distribution map of the analyte can be reconstituted from the mass spectra obtained. There is tremendous potential in its application especially in clinical field, such as biomarker discovery or pharmacokinetic study. However, vast majority of the work has been performed on frozen tissue sections, while it remains generally unpractical to produce frozen sections with clinically resected tumor samples. Here we report our novel sample preparation technique that enabled MS imaging from formalin-fixed paraffin embedded (FFPE) tissue section, including retrospective archive as old as 11 years. FFPE sections were first dewaxed with pre-warmed xylene, and exposed tissue surface was enzymatically digested in nanoliter scale droplets to retain analyte localization. As a result, we succeeded in obtaining MS images of peptide peaks derived from several proteins, identified by MS/MS analysis, using ovarian cancer FFPE sections. The qualities of mass spectra obtained by this method were not significantly different from those obtained from frozen sections. By this, we opened the door to retrospective study of past clinical cases in aim to discover molecular biomarker. The Japan Academy 2007-11 /pmc/articles/PMC3859273/ /pubmed/24367147 http://dx.doi.org/10.2183/pjab/83.205 Text en © 2007 The Japan Academy This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Aoki, Yutaka
Toyama, Atsuhiko
Shimada, Takashi
Sugita, Tetsuyoshi
Aoki, Chikage
Umino, Yukari
Suzuki, Atsushi
Aoki, Daisuke
Daigo, Yataro
Nakamura, Yusuke
Sato, Taka-Aki
A novel method for analyzing formalin-fixed paraffin embedded (FFPE) tissue sections by mass spectrometry imaging
title A novel method for analyzing formalin-fixed paraffin embedded (FFPE) tissue sections by mass spectrometry imaging
title_full A novel method for analyzing formalin-fixed paraffin embedded (FFPE) tissue sections by mass spectrometry imaging
title_fullStr A novel method for analyzing formalin-fixed paraffin embedded (FFPE) tissue sections by mass spectrometry imaging
title_full_unstemmed A novel method for analyzing formalin-fixed paraffin embedded (FFPE) tissue sections by mass spectrometry imaging
title_short A novel method for analyzing formalin-fixed paraffin embedded (FFPE) tissue sections by mass spectrometry imaging
title_sort novel method for analyzing formalin-fixed paraffin embedded (ffpe) tissue sections by mass spectrometry imaging
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859273/
https://www.ncbi.nlm.nih.gov/pubmed/24367147
http://dx.doi.org/10.2183/pjab/83.205
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