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Live slow-frozen human tumor tissues viable for 2D, 3D, ex vivo cultures and single-cell RNAseq
Biobanking of surplus human healthy and disease-derived tissues is essential for diagnostics and translational research. An enormous amount of formalin-fixed and paraffin-embedded (FFPE), Tissue-Tek OCT embedded or snap-frozen tissues are preserved in many biobanks worldwide and have been the basis...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616892/ https://www.ncbi.nlm.nih.gov/pubmed/36307545 http://dx.doi.org/10.1038/s42003-022-04025-0 |
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author | Restivo, Gaetana Tastanova, Aizhan Balázs, Zsolt Panebianco, Federica Diepenbruck, Maren Ercan, Caner Preca, Bodgan-T. Hafner, Jürg Weber, Walter P. Kurzeder, Christian Vetter, Marcus Soysal, Simone Münst Beisel, Christian Bentires-Alj, Mohamed Piscuoglio, Salvatore Krauthammer, Michael Levesque, Mitchell P. |
author_facet | Restivo, Gaetana Tastanova, Aizhan Balázs, Zsolt Panebianco, Federica Diepenbruck, Maren Ercan, Caner Preca, Bodgan-T. Hafner, Jürg Weber, Walter P. Kurzeder, Christian Vetter, Marcus Soysal, Simone Münst Beisel, Christian Bentires-Alj, Mohamed Piscuoglio, Salvatore Krauthammer, Michael Levesque, Mitchell P. |
author_sort | Restivo, Gaetana |
collection | PubMed |
description | Biobanking of surplus human healthy and disease-derived tissues is essential for diagnostics and translational research. An enormous amount of formalin-fixed and paraffin-embedded (FFPE), Tissue-Tek OCT embedded or snap-frozen tissues are preserved in many biobanks worldwide and have been the basis of translational studies. However, their usage is limited to assays that do not require viable cells. The access to intact and viable human material is a prerequisite for translational validation of basic research, for novel therapeutic target discovery, and functional testing. Here we show that surplus tissues from multiple solid human cancers directly slow-frozen after resection can subsequently be used for different types of methods including the establishment of 2D, 3D, and ex vivo cultures as well as single-cell RNA sequencing with similar results when compared to freshly analyzed material. |
format | Online Article Text |
id | pubmed-9616892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96168922022-10-30 Live slow-frozen human tumor tissues viable for 2D, 3D, ex vivo cultures and single-cell RNAseq Restivo, Gaetana Tastanova, Aizhan Balázs, Zsolt Panebianco, Federica Diepenbruck, Maren Ercan, Caner Preca, Bodgan-T. Hafner, Jürg Weber, Walter P. Kurzeder, Christian Vetter, Marcus Soysal, Simone Münst Beisel, Christian Bentires-Alj, Mohamed Piscuoglio, Salvatore Krauthammer, Michael Levesque, Mitchell P. Commun Biol Article Biobanking of surplus human healthy and disease-derived tissues is essential for diagnostics and translational research. An enormous amount of formalin-fixed and paraffin-embedded (FFPE), Tissue-Tek OCT embedded or snap-frozen tissues are preserved in many biobanks worldwide and have been the basis of translational studies. However, their usage is limited to assays that do not require viable cells. The access to intact and viable human material is a prerequisite for translational validation of basic research, for novel therapeutic target discovery, and functional testing. Here we show that surplus tissues from multiple solid human cancers directly slow-frozen after resection can subsequently be used for different types of methods including the establishment of 2D, 3D, and ex vivo cultures as well as single-cell RNA sequencing with similar results when compared to freshly analyzed material. Nature Publishing Group UK 2022-10-28 /pmc/articles/PMC9616892/ /pubmed/36307545 http://dx.doi.org/10.1038/s42003-022-04025-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access 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 http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Restivo, Gaetana Tastanova, Aizhan Balázs, Zsolt Panebianco, Federica Diepenbruck, Maren Ercan, Caner Preca, Bodgan-T. Hafner, Jürg Weber, Walter P. Kurzeder, Christian Vetter, Marcus Soysal, Simone Münst Beisel, Christian Bentires-Alj, Mohamed Piscuoglio, Salvatore Krauthammer, Michael Levesque, Mitchell P. Live slow-frozen human tumor tissues viable for 2D, 3D, ex vivo cultures and single-cell RNAseq |
title | Live slow-frozen human tumor tissues viable for 2D, 3D, ex vivo cultures and single-cell RNAseq |
title_full | Live slow-frozen human tumor tissues viable for 2D, 3D, ex vivo cultures and single-cell RNAseq |
title_fullStr | Live slow-frozen human tumor tissues viable for 2D, 3D, ex vivo cultures and single-cell RNAseq |
title_full_unstemmed | Live slow-frozen human tumor tissues viable for 2D, 3D, ex vivo cultures and single-cell RNAseq |
title_short | Live slow-frozen human tumor tissues viable for 2D, 3D, ex vivo cultures and single-cell RNAseq |
title_sort | live slow-frozen human tumor tissues viable for 2d, 3d, ex vivo cultures and single-cell rnaseq |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616892/ https://www.ncbi.nlm.nih.gov/pubmed/36307545 http://dx.doi.org/10.1038/s42003-022-04025-0 |
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