Zhang Liguo, Wang Chun-Yu, Yang Rui, Shi Jiandang, Fu Rong, Chen Linfeng, Klocker Helmut, Zhang Ju
Bioactive Materials Key Laboratory of the Ministry of Education, Institute for Molecular Biology, Nankai University, Tianjin, People's Republic of China.
Urol Oncol. 2008 Nov-Dec;26(6):634-40. doi: 10.1016/j.urolonc.2007.07.016. Epub 2008 Jan 14.
Reverse transcription-polymerase chain reaction (RT-PCR) was widely used to detect disseminated tumor cells. However, high percentages of false-positive cases have been reported. Herein, we developed a method to detect prostate cancer (PCa) micrometastasis by real-time quantitative RT-PCR.
Blood samples were obtained from 118 males, including 13 healthy volunteers, 17 patients with metastatic PCa, 20 patients with localized PCa, and 68 patients with BPH. RNA was isolated from blood samples of different patients. Real-time RT-PCR was used to quantify the copy number of PSA and PSMA. The primers and probe of PSMA were designed to specifically discriminate between PSMA and PSM', an alternatively spliced variant, mRNA.
There was significant difference in the PSA and PSMA mRNA levels among BPH, locally confined PCa, and metastatic PCa blood specimens. The real-time quantitative RT-PCR is sensitive, accurate, and has a high reproducibility within a wide dynamic range (10(3)-10(8)), which permits simultaneous quantitative analysis of samples with varying input concentrations.
This method improves accuracy and liability of assessment of disseminated prostate cancer cells in peripheral blood and is promising for clinical diagnosis purpose.
逆转录聚合酶链反应(RT-PCR)被广泛用于检测播散性肿瘤细胞。然而,已有报道称假阳性病例的比例较高。在此,我们开发了一种通过实时定量RT-PCR检测前列腺癌(PCa)微转移的方法。
采集了118名男性的血样,包括13名健康志愿者、17名转移性PCa患者、20名局限性PCa患者和68名良性前列腺增生(BPH)患者。从不同患者的血样中分离RNA。使用实时RT-PCR定量PSA和PSMA的拷贝数。PSMA的引物和探针被设计用于特异性区分PSMA和PSM'(一种选择性剪接变体mRNA)。
BPH、局限性PCa和转移性PCa血标本中的PSA和PSMA mRNA水平存在显著差异。实时定量RT-PCR灵敏、准确,在宽动态范围(10³ - 10⁸)内具有高重复性,可同时对不同输入浓度的样本进行定量分析。
该方法提高了外周血中播散性前列腺癌细胞评估的准确性和可靠性,对临床诊断具有应用前景。