Gelmini S, Orlando C, Sestini R, Vona G, Pinzani P, Ruocco L, Pazzagli M
Department of Clinical Physiopathology, University of Florence, Italy.
Clin Chem. 1997 May;43(5):752-8.
We describe a PCR-based assay for determining c-erbB-2 oncogene amplification in breast cancer in which we use the TaqMan system. Two fluorogenic probes anneal to the target between primers for c-erbB-2 and beta-globin genes and contain both a reporter dye (6-carboxy-fluorescein) and a quencher dye (6-carboxy-tetramethyl-rhodamine). During the extension phase of the PCR cycle, the 5'-->3' exonuclease activity of Taq polymerase cleaves the hybridized fluorogenic probe, resulting in an increase of fluorescence emission of the reporter dye that is quantitative for the amount of PCR product and, under appropriate conditions, for the amount of template. Assay performance showed adequate precision and a lower detection limit and good correlation with the results obtained in the same samples by a competitive PCR assay (n = 25, r = 0.94, P < 0.01). This homogeneous assay is time-saving, avoids usually cumbersome postamplification procedures (that can be additional sources of inaccuracy and contamination), and seems suitable for determination of c-erbB-2 oncogene amplification in tumor specimens.
我们描述了一种基于聚合酶链反应(PCR)的检测方法,用于测定乳腺癌中c-erbB-2癌基因的扩增情况,其中我们使用了TaqMan系统。两种荧光探针在c-erbB-2基因和β-珠蛋白基因的引物之间与靶序列退火,并同时包含一个报告染料(6-羧基荧光素)和一个淬灭染料(6-羧基四甲基罗丹明)。在PCR循环的延伸阶段,Taq聚合酶的5'→3'核酸外切酶活性切割杂交的荧光探针,导致报告染料的荧光发射增加,该增加与PCR产物的量定量相关,并且在适当条件下与模板的量定量相关。检测性能显示出足够的精密度、较低的检测限,并且与通过竞争性PCR检测在相同样本中获得的结果具有良好的相关性(n = 25,r = 0.94,P < 0.01)。这种均相检测方法节省时间,避免了通常繁琐的扩增后程序(这些程序可能是额外的不准确和污染来源),并且似乎适用于肿瘤标本中c-erbB-2癌基因扩增的测定。