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Cryopreserved biopsy tissues of rectal cancer liver metastasis for assessment of anticancer drug response in vitro and in vivo
Living tumors are of great scientific value for clinical medicine and basic research, especially for drug testing. An increasing number of drug tests fail due to the use of imperfect models. The aim of the present study was to develop a novel method combining vitrification-based cryopreservation of...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6967191/ https://www.ncbi.nlm.nih.gov/pubmed/31894341 http://dx.doi.org/10.3892/or.2019.7450 |
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author | Zhang, Yuan Huang, Wei-Jian Yang, Qiu-Rui Zhang, Hong-Dan Zhu, Xue-Jing Zeng, Min Zhou, Xu Wang, Zhen-Yu Li, Wei-Jian Jing, Hong-Shu Zhang, Xue-Bin Shi, Yao-Ping Hu, Hao Yan, He-Xin Li, Zong-Hai Zhai, Bo |
author_facet | Zhang, Yuan Huang, Wei-Jian Yang, Qiu-Rui Zhang, Hong-Dan Zhu, Xue-Jing Zeng, Min Zhou, Xu Wang, Zhen-Yu Li, Wei-Jian Jing, Hong-Shu Zhang, Xue-Bin Shi, Yao-Ping Hu, Hao Yan, He-Xin Li, Zong-Hai Zhai, Bo |
author_sort | Zhang, Yuan |
collection | PubMed |
description | Living tumors are of great scientific value for clinical medicine and basic research, especially for drug testing. An increasing number of drug tests fail due to the use of imperfect models. The aim of the present study was to develop a novel method combining vitrification-based cryopreservation of tumor biopsies and precision-cut slice cultivation for the assessment of anticancer drug responses. Biological characteristics of rectal cancer liver metastasis biopsies could be retained by vitrification-based cryopreservation. The patient-derived xenograft models were successfully established using both fresh and warmed biopsy tissues. Precision-cut slicing provided a similar three-dimensional architecture and heterogeneity to the original tumor. The positive drug responses in the xenograft model were consistent with those in precision-cut slice cultures in vitro. The present study demonstrated that live tumor biopsies could be preserved using vitrification-based cryopreservation. The warmed tissues developed xenograft tumors, which were also useful for either in vivo or in vitro anticancer drug testing. Precision-cut slices derived from the warmed tissues provided an efficient tool to assess anticancer drug response in vitro. |
format | Online Article Text |
id | pubmed-6967191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-69671912020-01-31 Cryopreserved biopsy tissues of rectal cancer liver metastasis for assessment of anticancer drug response in vitro and in vivo Zhang, Yuan Huang, Wei-Jian Yang, Qiu-Rui Zhang, Hong-Dan Zhu, Xue-Jing Zeng, Min Zhou, Xu Wang, Zhen-Yu Li, Wei-Jian Jing, Hong-Shu Zhang, Xue-Bin Shi, Yao-Ping Hu, Hao Yan, He-Xin Li, Zong-Hai Zhai, Bo Oncol Rep Articles Living tumors are of great scientific value for clinical medicine and basic research, especially for drug testing. An increasing number of drug tests fail due to the use of imperfect models. The aim of the present study was to develop a novel method combining vitrification-based cryopreservation of tumor biopsies and precision-cut slice cultivation for the assessment of anticancer drug responses. Biological characteristics of rectal cancer liver metastasis biopsies could be retained by vitrification-based cryopreservation. The patient-derived xenograft models were successfully established using both fresh and warmed biopsy tissues. Precision-cut slicing provided a similar three-dimensional architecture and heterogeneity to the original tumor. The positive drug responses in the xenograft model were consistent with those in precision-cut slice cultures in vitro. The present study demonstrated that live tumor biopsies could be preserved using vitrification-based cryopreservation. The warmed tissues developed xenograft tumors, which were also useful for either in vivo or in vitro anticancer drug testing. Precision-cut slices derived from the warmed tissues provided an efficient tool to assess anticancer drug response in vitro. D.A. Spandidos 2020-02 2019-12-30 /pmc/articles/PMC6967191/ /pubmed/31894341 http://dx.doi.org/10.3892/or.2019.7450 Text en Copyright: © Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Zhang, Yuan Huang, Wei-Jian Yang, Qiu-Rui Zhang, Hong-Dan Zhu, Xue-Jing Zeng, Min Zhou, Xu Wang, Zhen-Yu Li, Wei-Jian Jing, Hong-Shu Zhang, Xue-Bin Shi, Yao-Ping Hu, Hao Yan, He-Xin Li, Zong-Hai Zhai, Bo Cryopreserved biopsy tissues of rectal cancer liver metastasis for assessment of anticancer drug response in vitro and in vivo |
title | Cryopreserved biopsy tissues of rectal cancer liver metastasis for assessment of anticancer drug response in vitro and in vivo |
title_full | Cryopreserved biopsy tissues of rectal cancer liver metastasis for assessment of anticancer drug response in vitro and in vivo |
title_fullStr | Cryopreserved biopsy tissues of rectal cancer liver metastasis for assessment of anticancer drug response in vitro and in vivo |
title_full_unstemmed | Cryopreserved biopsy tissues of rectal cancer liver metastasis for assessment of anticancer drug response in vitro and in vivo |
title_short | Cryopreserved biopsy tissues of rectal cancer liver metastasis for assessment of anticancer drug response in vitro and in vivo |
title_sort | cryopreserved biopsy tissues of rectal cancer liver metastasis for assessment of anticancer drug response in vitro and in vivo |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6967191/ https://www.ncbi.nlm.nih.gov/pubmed/31894341 http://dx.doi.org/10.3892/or.2019.7450 |
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