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...
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Veröffentlicht in: | Oncology reports 2020-02, Vol.43 (2), p.405-414 |
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creator | 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 |
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. |
doi_str_mv | 10.3892/or.2019.7450 |
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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.</description><identifier>ISSN: 1021-335X</identifier><identifier>EISSN: 1791-2431</identifier><identifier>DOI: 10.3892/or.2019.7450</identifier><identifier>PMID: 31894341</identifier><language>eng</language><publisher>Greece: Spandidos Publications</publisher><subject>Analysis ; Biopsy ; Cancer metastasis ; Chemotherapy ; Colorectal cancer ; Cryopreservation ; Development and progression ; Drug testing ; Gene expression ; Genomes ; Liver cancer ; Medical research ; Metastasis ; Nitrogen ; Novels ; Oxalic acid ; Tumors</subject><ispartof>Oncology reports, 2020-02, Vol.43 (2), p.405-414</ispartof><rights>COPYRIGHT 2020 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2020</rights><rights>Copyright: © Zhang et al. 2020</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31894341$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Yuan</creatorcontrib><creatorcontrib>Huang, Wei-Jian</creatorcontrib><creatorcontrib>Yang, Qiu-Rui</creatorcontrib><creatorcontrib>Zhang, Hong-Dan</creatorcontrib><creatorcontrib>Zhu, Xue-Jing</creatorcontrib><creatorcontrib>Zeng, Min</creatorcontrib><creatorcontrib>Zhou, Xu</creatorcontrib><creatorcontrib>Wang, Zhen-Yu</creatorcontrib><creatorcontrib>Li, Wei-Jian</creatorcontrib><creatorcontrib>Jing, Hong-Shu</creatorcontrib><creatorcontrib>Zhang, Xue-Bin</creatorcontrib><creatorcontrib>Shi, Yao-Ping</creatorcontrib><creatorcontrib>Hu, Hao</creatorcontrib><creatorcontrib>Yan, He-Xin</creatorcontrib><creatorcontrib>Li, Zong-Hai</creatorcontrib><creatorcontrib>Zhai, Bo</creatorcontrib><title>Cryopreserved biopsy tissues of rectal cancer liver metastasis for assessment of anticancer drug response in vitro and in vivo</title><title>Oncology reports</title><addtitle>Oncol Rep</addtitle><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.</description><subject>Analysis</subject><subject>Biopsy</subject><subject>Cancer metastasis</subject><subject>Chemotherapy</subject><subject>Colorectal cancer</subject><subject>Cryopreservation</subject><subject>Development and progression</subject><subject>Drug testing</subject><subject>Gene expression</subject><subject>Genomes</subject><subject>Liver cancer</subject><subject>Medical research</subject><subject>Metastasis</subject><subject>Nitrogen</subject><subject>Novels</subject><subject>Oxalic acid</subject><subject>Tumors</subject><issn>1021-335X</issn><issn>1791-2431</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNptkluL1DAUx4so7jr65rMUBPHBjrk0bfKysAzrBRZ8UfAtpOnJTJa2GXPawrz5UfwsfrJN2XHdEUnI9Xf-J-fkZNlLStZcKvY-xDUjVK3rUpBH2TmtFS1YyenjtCaMFpyL72fZM8QbQlhNKvU0O-NUqpKX9Dz7uYmHsI-AEGdo88aHPR7y0SNOgHlweQQ7mi63ZrAQ887PaexhNJi6x9yFmBtEQOxhGBcDM4z-SLdx2iYB3IcBIffD71-zH2NISHvczeF59sSZDuHFcV5l3z5cfd18Kq6_fPy8ubwubFnVYyFY3VjJhZSOl00rSqUIc-A4l46JpiVWpIgqRUSlHMjKSilVYyhYZlRLBV9lF3e6-6npobXptdF0eh99b-JBB-P16c3gd3obZl2pqqaKJoG3R4EYfqTkjLr3aKHrzABhQs04Z0QSwRZfr_9Bb8IUhxReokrGCBeU_6W2pgPtBxeSX7uI6suKcpJCTP-4ytb_oVJrofc2DOB8Oj8xePPAYAemG3cYumn06RdOwXd3oI0BMYK7TwYleiktHaJeSksvpZXwVw8TeA__qSV-C719y9w</recordid><startdate>20200201</startdate><enddate>20200201</enddate><creator>Zhang, Yuan</creator><creator>Huang, Wei-Jian</creator><creator>Yang, Qiu-Rui</creator><creator>Zhang, Hong-Dan</creator><creator>Zhu, Xue-Jing</creator><creator>Zeng, Min</creator><creator>Zhou, Xu</creator><creator>Wang, Zhen-Yu</creator><creator>Li, Wei-Jian</creator><creator>Jing, Hong-Shu</creator><creator>Zhang, Xue-Bin</creator><creator>Shi, Yao-Ping</creator><creator>Hu, Hao</creator><creator>Yan, He-Xin</creator><creator>Li, Zong-Hai</creator><creator>Zhai, Bo</creator><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><general>D.A. Spandidos</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200201</creationdate><title>Cryopreserved biopsy tissues of rectal cancer liver metastasis for assessment of anticancer drug response in vitro and in vivo</title><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></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-527bc83588f34bd549902fef338f25bd0c5943690569fe86c8889ba1ec2a9d153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Analysis</topic><topic>Biopsy</topic><topic>Cancer metastasis</topic><topic>Chemotherapy</topic><topic>Colorectal cancer</topic><topic>Cryopreservation</topic><topic>Development and progression</topic><topic>Drug testing</topic><topic>Gene expression</topic><topic>Genomes</topic><topic>Liver cancer</topic><topic>Medical research</topic><topic>Metastasis</topic><topic>Nitrogen</topic><topic>Novels</topic><topic>Oxalic acid</topic><topic>Tumors</topic><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Yuan</creatorcontrib><creatorcontrib>Huang, Wei-Jian</creatorcontrib><creatorcontrib>Yang, Qiu-Rui</creatorcontrib><creatorcontrib>Zhang, Hong-Dan</creatorcontrib><creatorcontrib>Zhu, Xue-Jing</creatorcontrib><creatorcontrib>Zeng, Min</creatorcontrib><creatorcontrib>Zhou, Xu</creatorcontrib><creatorcontrib>Wang, Zhen-Yu</creatorcontrib><creatorcontrib>Li, Wei-Jian</creatorcontrib><creatorcontrib>Jing, Hong-Shu</creatorcontrib><creatorcontrib>Zhang, Xue-Bin</creatorcontrib><creatorcontrib>Shi, Yao-Ping</creatorcontrib><creatorcontrib>Hu, Hao</creatorcontrib><creatorcontrib>Yan, He-Xin</creatorcontrib><creatorcontrib>Li, Zong-Hai</creatorcontrib><creatorcontrib>Zhai, Bo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Yuan</au><au>Huang, Wei-Jian</au><au>Yang, Qiu-Rui</au><au>Zhang, Hong-Dan</au><au>Zhu, Xue-Jing</au><au>Zeng, Min</au><au>Zhou, Xu</au><au>Wang, Zhen-Yu</au><au>Li, Wei-Jian</au><au>Jing, Hong-Shu</au><au>Zhang, Xue-Bin</au><au>Shi, Yao-Ping</au><au>Hu, Hao</au><au>Yan, He-Xin</au><au>Li, Zong-Hai</au><au>Zhai, Bo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cryopreserved biopsy tissues of rectal cancer liver metastasis for assessment of anticancer drug response in vitro and in vivo</atitle><jtitle>Oncology reports</jtitle><addtitle>Oncol Rep</addtitle><date>2020-02-01</date><risdate>2020</risdate><volume>43</volume><issue>2</issue><spage>405</spage><epage>414</epage><pages>405-414</pages><issn>1021-335X</issn><eissn>1791-2431</eissn><abstract>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.</abstract><cop>Greece</cop><pub>Spandidos Publications</pub><pmid>31894341</pmid><doi>10.3892/or.2019.7450</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Biopsy Cancer metastasis Chemotherapy Colorectal cancer Cryopreservation Development and progression Drug testing Gene expression Genomes Liver cancer Medical research Metastasis Nitrogen Novels Oxalic acid Tumors |
title | Cryopreserved biopsy tissues of rectal cancer liver metastasis for assessment of anticancer drug response in vitro and in vivo |
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