一种高通量和高度自动化的遗传毒性筛选试验。

ALTEX Pub Date : 2022-01-01 Epub Date: 2021-09-28 DOI:10.14573/altex.2102121
Renxiang Chen, Yun-Tien Lin, Albert J Fornace, Heng-Hong Li
{"title":"一种高通量和高度自动化的遗传毒性筛选试验。","authors":"Renxiang Chen,&nbsp;Yun-Tien Lin,&nbsp;Albert J Fornace,&nbsp;Heng-Hong Li","doi":"10.14573/altex.2102121","DOIUrl":null,"url":null,"abstract":"<p><p>The increasing number of compounds under development and chemicals in commerce that require safety assessments pose a serious challenge for regulatory agencies worldwide. In vitro screening using toxicogenomic biomarkers has been proposed as a first-tier screen in chemical assessment and has been endorsed internationally. We previously developed, evaluated, and validated an in vitro transcriptomic biomarker responsive to DNA damage-inducing (DDI) agents, namely TGx-DDI, for genotoxicity testing in human cells and demonstrated the feasibility of using TGx-DDI in a medium-throughput, cell-based genotoxicity testing system by implementing this biomarker with the Nanostring nCounter system. In this current study, we took advantage of Nanostring nCounter Plexset technology to develop a highly auto­mated, multiplexed, and high-throughput genotoxicity testing assay, designated the TGx-DDI Plexset assay, which can increase the screening efficiency eight-fold compared to standard nCounter technology while decreasing the hands-on time. We demonstrate the high-throughput capability of this assay by eliminating concentration determination and RNA extraction steps without compromising the specificity and sensitivity of TGx-DDI. Thus, we propose that this simple, highly automated, multiplexed high-throughput pipeline can be widely used in chemical screening and assessment.</p>","PeriodicalId":520550,"journal":{"name":"ALTEX","volume":" ","pages":"71-81"},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"A high-throughput and highly automated genotoxicity screening assay.\",\"authors\":\"Renxiang Chen,&nbsp;Yun-Tien Lin,&nbsp;Albert J Fornace,&nbsp;Heng-Hong Li\",\"doi\":\"10.14573/altex.2102121\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The increasing number of compounds under development and chemicals in commerce that require safety assessments pose a serious challenge for regulatory agencies worldwide. In vitro screening using toxicogenomic biomarkers has been proposed as a first-tier screen in chemical assessment and has been endorsed internationally. We previously developed, evaluated, and validated an in vitro transcriptomic biomarker responsive to DNA damage-inducing (DDI) agents, namely TGx-DDI, for genotoxicity testing in human cells and demonstrated the feasibility of using TGx-DDI in a medium-throughput, cell-based genotoxicity testing system by implementing this biomarker with the Nanostring nCounter system. In this current study, we took advantage of Nanostring nCounter Plexset technology to develop a highly auto­mated, multiplexed, and high-throughput genotoxicity testing assay, designated the TGx-DDI Plexset assay, which can increase the screening efficiency eight-fold compared to standard nCounter technology while decreasing the hands-on time. We demonstrate the high-throughput capability of this assay by eliminating concentration determination and RNA extraction steps without compromising the specificity and sensitivity of TGx-DDI. Thus, we propose that this simple, highly automated, multiplexed high-throughput pipeline can be widely used in chemical screening and assessment.</p>\",\"PeriodicalId\":520550,\"journal\":{\"name\":\"ALTEX\",\"volume\":\" \",\"pages\":\"71-81\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ALTEX\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.14573/altex.2102121\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2021/9/28 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ALTEX","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.14573/altex.2102121","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/9/28 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

摘要

越来越多的正在开发的化合物和商业化学品需要进行安全评估,这对世界各地的监管机构构成了严峻的挑战。使用毒物基因组生物标志物进行体外筛选已被提议作为化学评估的一级筛选,并已得到国际上的认可。我们之前开发、评估和验证了一种对DNA损伤诱导(DDI)药物有反应的体外转录组生物标志物,即TGx-DDI,用于人类细胞的遗传毒性测试,并通过将TGx-DDI生物标志物与Nanostring nCounter系统结合使用,证明了在中等通量、基于细胞的遗传毒性测试系统中使用TGx-DDI的可行性。在目前的研究中,我们利用Nanostring nCounter Plexset技术开发了一种高度自动化、多路复用、高通量的遗传毒性检测方法,称为TGx-DDI Plexset,与标准的nCounter技术相比,该方法可以将筛选效率提高8倍,同时减少了操作时间。我们通过消除浓度测定和RNA提取步骤而不影响TGx-DDI的特异性和敏感性,证明了该检测的高通量能力。因此,我们建议这种简单、高度自动化、多路复用的高通量管道可以广泛用于化学筛选和评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A high-throughput and highly automated genotoxicity screening assay.

The increasing number of compounds under development and chemicals in commerce that require safety assessments pose a serious challenge for regulatory agencies worldwide. In vitro screening using toxicogenomic biomarkers has been proposed as a first-tier screen in chemical assessment and has been endorsed internationally. We previously developed, evaluated, and validated an in vitro transcriptomic biomarker responsive to DNA damage-inducing (DDI) agents, namely TGx-DDI, for genotoxicity testing in human cells and demonstrated the feasibility of using TGx-DDI in a medium-throughput, cell-based genotoxicity testing system by implementing this biomarker with the Nanostring nCounter system. In this current study, we took advantage of Nanostring nCounter Plexset technology to develop a highly auto­mated, multiplexed, and high-throughput genotoxicity testing assay, designated the TGx-DDI Plexset assay, which can increase the screening efficiency eight-fold compared to standard nCounter technology while decreasing the hands-on time. We demonstrate the high-throughput capability of this assay by eliminating concentration determination and RNA extraction steps without compromising the specificity and sensitivity of TGx-DDI. Thus, we propose that this simple, highly automated, multiplexed high-throughput pipeline can be widely used in chemical screening and assessment.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信