Pohl Gudrun, Shih Ie-Ming
Department of Pathology, 418 North Bond Street, B-315, Baltimore, MD 21231, USA.
Expert Rev Mol Diagn. 2004 Jan;4(1):41-7. doi: 10.1586/14737159.4.1.41.
Digital PCR represents an example of the power of PCR and provides unprecedented opportunities for molecular genetic analysis in cancer. The technique is to amplify a single DNA template from minimally diluted samples, therefore generating amplicons that are exclusively derived from one template and can be detected with different fluorophores or sequencing to discriminate different alleles (e.g., wild type vs. mutant or paternal vs. maternal alleles). Thus, digital PCR transforms the exponential, analog signals obtained from conventional PCR to linear, digital signals, allowing statistical analysis of the PCR product. Digital PCR has been applied in quantification of mutant alleles and detection of allelic imbalance in clinical specimens, providing a promising molecular diagnostic tool for cancer detection. The scope of this article is to review the principles of digital PCR and its practical applications in cancer research and in the molecular diagnosis of cancer.
数字PCR体现了PCR技术的强大功能,为癌症分子遗传学分析提供了前所未有的机遇。该技术是从最低限度稀释的样本中扩增单个DNA模板,从而产生仅源自一个模板的扩增子,并且可以用不同的荧光团或测序来检测,以区分不同的等位基因(例如,野生型与突变型或父本与母本等位基因)。因此,数字PCR将从传统PCR获得的指数型模拟信号转变为线性数字信号,从而允许对PCR产物进行统计分析。数字PCR已应用于临床样本中突变等位基因的定量和等位基因不平衡的检测,为癌症检测提供了一种有前景的分子诊断工具。本文的范围是综述数字PCR的原理及其在癌症研究和癌症分子诊断中的实际应用。