• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

外周血采集:基因表达谱分析的第一步。

Peripheral blood collection: the first step towards gene expression profiling.

作者信息

Franken Carmen, Remy Sylvie, Lambrechts Nathalie, Hollanders Karen, Den Hond Elly, Schoeters Greet

机构信息

a Unit Environmental Risk and Health, Flemish Institute for Technological Research (VITO NV) , Mol , Belgium ;

b Department of Biomedical Sciences ;

出版信息

Biomarkers. 2016 Jul;21(5):458-65. doi: 10.3109/1354750X.2016.1153721. Epub 2016 Mar 17.

DOI:10.3109/1354750X.2016.1153721
PMID:26984061
Abstract

A crucial challenge for gene expression analysis in human biomonitoring studies on whole blood samples is rapid sample handling and mRNA stabilization. This study was designed to evaluate the impact of short bench times (less than 30 min) on yield, quality and gene expression of mRNA in the presence of different stabilization buffers (Tempus(TM) Blood RNA tube and RNAlater(®) Stabilization Reagent). Microarray analyzes showed significant changes over short periods of time in expression of a considerate part of the transcriptome (2356 genes) with a prominent role for NFкB-, cancer- and glucocorticoid-mediated networks, and specifically interleukin-8 (IL-8). These findings suggest that even short bench times affect gene expression, requiring to carry out blood collection in a strictly standardized way.

摘要

在全血样本的人体生物监测研究中,基因表达分析面临的一个关键挑战是快速的样本处理和mRNA稳定化。本研究旨在评估在不同稳定缓冲液(Tempus™血液RNA管和RNAlater®稳定试剂)存在的情况下,短时间放置(少于30分钟)对mRNA产量、质量和基因表达的影响。微阵列分析显示,在短时间内,转录组中相当一部分(2356个基因)的表达发生了显著变化,其中NFкB、癌症和糖皮质激素介导的网络,特别是白细胞介素-8(IL-8)发挥了重要作用。这些发现表明,即使是短时间放置也会影响基因表达,这就要求以严格标准化的方式进行血液采集。

相似文献

1
Peripheral blood collection: the first step towards gene expression profiling.外周血采集:基因表达谱分析的第一步。
Biomarkers. 2016 Jul;21(5):458-65. doi: 10.3109/1354750X.2016.1153721. Epub 2016 Mar 17.
2
Differential gene expression profiles are dependent upon method of peripheral blood collection and RNA isolation.差异基因表达谱取决于外周血采集方法和RNA分离方法。
BMC Genomics. 2008 Oct 10;9:474. doi: 10.1186/1471-2164-9-474.
3
Preanalytical robustness of blood collection tubes with RNA stabilizers.含 RNA 稳定剂的血液采集管的分析前稳定性。
Clin Chem Lab Med. 2019 Sep 25;57(10):1522-1529. doi: 10.1515/cclm-2019-0170.
4
Investigating gene expression profiles of whole blood and peripheral blood mononuclear cells using multiple collection and processing methods.采用多种采集和处理方法研究全血和外周血单个核细胞的基因表达谱。
PLoS One. 2019 Dec 6;14(12):e0225137. doi: 10.1371/journal.pone.0225137. eCollection 2019.
5
A highly standardized, robust, and cost-effective method for genome-wide transcriptome analysis of peripheral blood applicable to large-scale clinical trials.一种高度标准化、稳健且具有成本效益的方法,用于对外周血进行全基因组转录组分析,适用于大规模临床试验。
Genomics. 2006 May;87(5):653-64. doi: 10.1016/j.ygeno.2005.11.010. Epub 2006 Jan 4.
6
Optimized blood cell profiling method for genomic biomarker discovery using high-density microarray.使用高密度微阵列进行基因组生物标志物发现的优化血细胞分析方法
Biomarkers. 2005 Jul-Aug;10(4):310-20. doi: 10.1080/13547500500218583.
7
Gene expression differences between PAXgene and Tempus blood RNA tubes are highly reproducible between independent samples and biobanks.PAXgene血RNA管和Tempus血RNA管之间的基因表达差异在独立样本和生物样本库之间具有高度可重复性。
BMC Res Notes. 2017 Mar 23;10(1):136. doi: 10.1186/s13104-017-2455-6.
8
Impact of blood collection and processing on peripheral blood gene expression profiling in type 1 diabetes.血液采集与处理对1型糖尿病患者外周血基因表达谱的影响。
BMC Genomics. 2017 Aug 18;18(1):636. doi: 10.1186/s12864-017-3949-2.
9
RNA stabilization of peripheral blood and profiling by bead chip analysis.外周血RNA稳定及通过微珠芯片分析进行谱分析
Methods Mol Biol. 2009;496:175-210. doi: 10.1007/978-1-59745-553-4_13.
10
SPIDIA-RNA: first external quality assessment for the pre-analytical phase of blood samples used for RNA based analyses.SPIDIA-RNA:用于基于 RNA 分析的血液样本前分析阶段的首次外部质量评估。
Methods. 2013 Jan;59(1):20-31. doi: 10.1016/j.ymeth.2012.10.007. Epub 2012 Oct 27.

引用本文的文献

1
The Use of a Novel Container for Secured Transport and Storage of Biological Material for Quantitative Human RNA Analysis.一种用于安全运输和储存生物材料以进行人类RNA定量分析的新型容器的应用
Int J Mol Sci. 2024 Dec 30;26(1):228. doi: 10.3390/ijms26010228.
2
Investigating Whether a Combination of Electro-Encephalography and Gene Expression Profiling Can Predict the Risk of Chronic Pain: A Protocol for an Observational Prospective Cohort Study.研究脑电图与基因表达谱相结合是否能预测慢性疼痛风险:一项观察性前瞻性队列研究方案
Brain Sci. 2024 Jun 26;14(7):641. doi: 10.3390/brainsci14070641.
3
Circular RNAs in peripheral blood mononuclear cells are more stable than linear RNAs upon sample processing delay.
循环 RNA 在血液单核细胞中比线性 RNA 更稳定,即使在样本处理延迟的情况下也是如此。
J Cell Mol Med. 2022 Oct;26(19):5021-5032. doi: 10.1111/jcmm.17525. Epub 2022 Aug 30.
4
The impact of pre-freezing storage time and temperature on gene expression of blood collected in EDTA tubes.EDTA 采血管中血液基因表达受预冻储存时间和温度的影响
Mol Biol Rep. 2022 Jun;49(6):4709-4718. doi: 10.1007/s11033-022-07320-5. Epub 2022 Mar 12.
5
Influence of storage conditions of small volumes of blood on immune transcriptomic profiles.少量血液储存条件对免疫转录组图谱的影响。
BMC Res Notes. 2020 Mar 13;13(1):150. doi: 10.1186/s13104-020-04980-z.
6
Comparison of procedures for RNA-extraction from peripheral blood mononuclear cells.比较从外周血单核细胞中提取 RNA 的程序。
PLoS One. 2020 Feb 21;15(2):e0229423. doi: 10.1371/journal.pone.0229423. eCollection 2020.
7
Investigating gene expression profiles of whole blood and peripheral blood mononuclear cells using multiple collection and processing methods.采用多种采集和处理方法研究全血和外周血单个核细胞的基因表达谱。
PLoS One. 2019 Dec 6;14(12):e0225137. doi: 10.1371/journal.pone.0225137. eCollection 2019.
8
Impact of blood collection and processing on peripheral blood gene expression profiling in type 1 diabetes.血液采集与处理对1型糖尿病患者外周血基因表达谱的影响。
BMC Genomics. 2017 Aug 18;18(1):636. doi: 10.1186/s12864-017-3949-2.