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用于癌症诊断的小型化聚合酶链反应系统。

Miniaturized PCR systems for cancer diagnosis.

作者信息

Day Philip J R

机构信息

Quantitative Analytical Genomics, The Manchester Interdisciplinary Biocentre, University of Manchester, Manchester, UK.

出版信息

Biochem Soc Trans. 2009 Apr;37(Pt 2):424-6. doi: 10.1042/BST0370424.

Abstract

PCR retains a pivotal role in making accessible marker nucleic acid sequences for ready analysis in cancer diagnosis. For certain cancers such as acute lymphoblastic leukaemia, the application of quantitative procedures to assess and subsequently direct therapy has given rise to the slowly maturing field of MRD (minimal residual disease) management. Although excellent protocols exist for performing these analyses, akin to all PCR procedures the limit of detection can vary markedly between laboratories. The present paper is an overview that describes how the analytical field relating to miniaturization is likely to identify the missing link that integrates sample processing with downstream PCR, analysis and eventual therapy. Miniaturized devices are suited to the multi-parallelized handling of defined numbers of cells, and PCR-based microfluidic procedures have become reasonably established. The integration of sample processing and PCR in microfluidic devices is beginning to offer reproducible quantitative data that relate the number of biomarker nucleic acids to the defined analysed cell or cells for meaningful clinical assessment. The application of MRD may, through integrated miniaturized PCR, become more reliable and routine with additional applications in defining disease threshold levels for other cancer types. These enabling integrated platforms may facilitate biomarker measurements to predict the response and outcome, which are also of current interest for personalized medical care.

摘要

在癌症诊断中,聚合酶链反应(PCR)对于获取可用于即时分析的标记核酸序列仍起着关键作用。对于某些癌症,如急性淋巴细胞白血病,应用定量程序来评估并随后指导治疗催生了微小残留病(MRD)管理这一逐渐成熟的领域。尽管存在用于进行这些分析的优秀方案,但与所有PCR程序一样,各实验室之间的检测限可能存在显著差异。本文是一篇综述,描述了与小型化相关的分析领域如何可能找到将样品处理与下游PCR、分析及最终治疗整合起来的缺失环节。小型化设备适合对特定数量的细胞进行多平行处理,基于PCR的微流控程序已得到相当程度的确立。微流控设备中样品处理与PCR的整合开始提供可重复的定量数据,这些数据将生物标志物核酸的数量与经定义分析的一个或多个细胞相关联,以进行有意义的临床评估。通过整合的小型化PCR,MRD的应用在定义其他癌症类型的疾病阈值水平方面可能会变得更加可靠且常规。这些具备整合功能的平台可能会促进生物标志物测量,以预测反应和结果,这也是当前个性化医疗所关注的。

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