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Biobanking: Objectives, Requirements, and Future Challenges—Experiences from the Munich Vascular Biobank

Collecting biological tissue samples in a biobank grants a unique opportunity to validate diagnostic and therapeutic strategies for translational and clinical research. In the present work, we provide our long-standing experience in establishing and maintaining a biobank of vascular tissue samples,...

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Autores principales: Pelisek, Jaroslav, Hegenloh, Renate, Bauer, Sabine, Metschl, Susanne, Pauli, Jessica, Glukha, Nadiya, Busch, Albert, Reutersberg, Benedikt, Kallmayer, Michael, Trenner, Matthias, Wendorff, Heiko, Tsantilas, Pavlos, Schmid, Sofie, Knappich, Christoph, Schaeffer, Christoph, Stadlbauer, Thomas, Biro, Gabor, Wertern, Uta, Meisner, Franz, Stoklasa, Kerstin, Menges, Anna-Leonie, Radu, Oksana, Dallmann-Sieber, Sabine, Karlas, Angelos, Knipfer, Eva, Reeps, Christian, Zimmermann, Alexander, Maegdefessel, Lars, Eckstein, Hans-Henning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406278/
https://www.ncbi.nlm.nih.gov/pubmed/30781475
http://dx.doi.org/10.3390/jcm8020251
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author Pelisek, Jaroslav
Hegenloh, Renate
Bauer, Sabine
Metschl, Susanne
Pauli, Jessica
Glukha, Nadiya
Busch, Albert
Reutersberg, Benedikt
Kallmayer, Michael
Trenner, Matthias
Wendorff, Heiko
Tsantilas, Pavlos
Schmid, Sofie
Knappich, Christoph
Schaeffer, Christoph
Stadlbauer, Thomas
Biro, Gabor
Wertern, Uta
Meisner, Franz
Stoklasa, Kerstin
Menges, Anna-Leonie
Radu, Oksana
Dallmann-Sieber, Sabine
Karlas, Angelos
Knipfer, Eva
Reeps, Christian
Zimmermann, Alexander
Maegdefessel, Lars
Eckstein, Hans-Henning
author_facet Pelisek, Jaroslav
Hegenloh, Renate
Bauer, Sabine
Metschl, Susanne
Pauli, Jessica
Glukha, Nadiya
Busch, Albert
Reutersberg, Benedikt
Kallmayer, Michael
Trenner, Matthias
Wendorff, Heiko
Tsantilas, Pavlos
Schmid, Sofie
Knappich, Christoph
Schaeffer, Christoph
Stadlbauer, Thomas
Biro, Gabor
Wertern, Uta
Meisner, Franz
Stoklasa, Kerstin
Menges, Anna-Leonie
Radu, Oksana
Dallmann-Sieber, Sabine
Karlas, Angelos
Knipfer, Eva
Reeps, Christian
Zimmermann, Alexander
Maegdefessel, Lars
Eckstein, Hans-Henning
author_sort Pelisek, Jaroslav
collection PubMed
description Collecting biological tissue samples in a biobank grants a unique opportunity to validate diagnostic and therapeutic strategies for translational and clinical research. In the present work, we provide our long-standing experience in establishing and maintaining a biobank of vascular tissue samples, including the evaluation of tissue quality, especially in formalin-fixed paraffin-embedded specimens (FFPE). Our Munich Vascular Biobank includes, thus far, vascular biomaterial from patients with high-grade carotid artery stenosis (n = 1567), peripheral arterial disease (n = 703), and abdominal aortic aneurysm (n = 481) from our Department of Vascular and Endovascular Surgery (January 2004–December 2018). Vascular tissue samples are continuously processed and characterized to assess tissue morphology, histological quality, cellular composition, inflammation, calcification, neovascularization, and the content of elastin and collagen fibers. Atherosclerotic plaques are further classified in accordance with the American Heart Association (AHA), and plaque stability is determined. In order to assess the quality of RNA from FFPE tissue samples over time (2009–2018), RNA integrity number (RIN) and the extent of RNA fragmentation were evaluated. Expression analysis was performed with two housekeeping genes—glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and beta-actin (ACTB)—using TaqMan-based quantitative reverse-transcription polymerase chain reaction (qRT)-PCR. FFPE biospecimens demonstrated unaltered RNA stability over time for up to 10 years. Furthermore, we provide a protocol for processing tissue samples in our Munich Vascular Biobank. In this work, we demonstrate that biobanking is an important tool not only for scientific research but also for clinical usage and personalized medicine.
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spelling pubmed-64062782019-03-22 Biobanking: Objectives, Requirements, and Future Challenges—Experiences from the Munich Vascular Biobank Pelisek, Jaroslav Hegenloh, Renate Bauer, Sabine Metschl, Susanne Pauli, Jessica Glukha, Nadiya Busch, Albert Reutersberg, Benedikt Kallmayer, Michael Trenner, Matthias Wendorff, Heiko Tsantilas, Pavlos Schmid, Sofie Knappich, Christoph Schaeffer, Christoph Stadlbauer, Thomas Biro, Gabor Wertern, Uta Meisner, Franz Stoklasa, Kerstin Menges, Anna-Leonie Radu, Oksana Dallmann-Sieber, Sabine Karlas, Angelos Knipfer, Eva Reeps, Christian Zimmermann, Alexander Maegdefessel, Lars Eckstein, Hans-Henning J Clin Med Article Collecting biological tissue samples in a biobank grants a unique opportunity to validate diagnostic and therapeutic strategies for translational and clinical research. In the present work, we provide our long-standing experience in establishing and maintaining a biobank of vascular tissue samples, including the evaluation of tissue quality, especially in formalin-fixed paraffin-embedded specimens (FFPE). Our Munich Vascular Biobank includes, thus far, vascular biomaterial from patients with high-grade carotid artery stenosis (n = 1567), peripheral arterial disease (n = 703), and abdominal aortic aneurysm (n = 481) from our Department of Vascular and Endovascular Surgery (January 2004–December 2018). Vascular tissue samples are continuously processed and characterized to assess tissue morphology, histological quality, cellular composition, inflammation, calcification, neovascularization, and the content of elastin and collagen fibers. Atherosclerotic plaques are further classified in accordance with the American Heart Association (AHA), and plaque stability is determined. In order to assess the quality of RNA from FFPE tissue samples over time (2009–2018), RNA integrity number (RIN) and the extent of RNA fragmentation were evaluated. Expression analysis was performed with two housekeeping genes—glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and beta-actin (ACTB)—using TaqMan-based quantitative reverse-transcription polymerase chain reaction (qRT)-PCR. FFPE biospecimens demonstrated unaltered RNA stability over time for up to 10 years. Furthermore, we provide a protocol for processing tissue samples in our Munich Vascular Biobank. In this work, we demonstrate that biobanking is an important tool not only for scientific research but also for clinical usage and personalized medicine. MDPI 2019-02-16 /pmc/articles/PMC6406278/ /pubmed/30781475 http://dx.doi.org/10.3390/jcm8020251 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pelisek, Jaroslav
Hegenloh, Renate
Bauer, Sabine
Metschl, Susanne
Pauli, Jessica
Glukha, Nadiya
Busch, Albert
Reutersberg, Benedikt
Kallmayer, Michael
Trenner, Matthias
Wendorff, Heiko
Tsantilas, Pavlos
Schmid, Sofie
Knappich, Christoph
Schaeffer, Christoph
Stadlbauer, Thomas
Biro, Gabor
Wertern, Uta
Meisner, Franz
Stoklasa, Kerstin
Menges, Anna-Leonie
Radu, Oksana
Dallmann-Sieber, Sabine
Karlas, Angelos
Knipfer, Eva
Reeps, Christian
Zimmermann, Alexander
Maegdefessel, Lars
Eckstein, Hans-Henning
Biobanking: Objectives, Requirements, and Future Challenges—Experiences from the Munich Vascular Biobank
title Biobanking: Objectives, Requirements, and Future Challenges—Experiences from the Munich Vascular Biobank
title_full Biobanking: Objectives, Requirements, and Future Challenges—Experiences from the Munich Vascular Biobank
title_fullStr Biobanking: Objectives, Requirements, and Future Challenges—Experiences from the Munich Vascular Biobank
title_full_unstemmed Biobanking: Objectives, Requirements, and Future Challenges—Experiences from the Munich Vascular Biobank
title_short Biobanking: Objectives, Requirements, and Future Challenges—Experiences from the Munich Vascular Biobank
title_sort biobanking: objectives, requirements, and future challenges—experiences from the munich vascular biobank
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406278/
https://www.ncbi.nlm.nih.gov/pubmed/30781475
http://dx.doi.org/10.3390/jcm8020251
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