Skvortsova T E, Rykova E Y, Tamkovich S N, Bryzgunova O E, Starikov A V, Kuznetsova N P, Vlassov V V, Laktionov P P
Institute of Chemical Biology and Fundamental Medicine, SD RAS, 8, Lavrentiev ave., Novosibirsk 630090, Russia.
Br J Cancer. 2006 May 22;94(10):1492-5. doi: 10.1038/sj.bjc.6603117.
Tumour development is characterised by the increased circulating DNA (cirDNA) concentration and by tumour-related changes in blood plasma DNA. Concentration of cirDNA and methylation of RARbeta2, RASSF1A and HIC-1 gene promoters were investigated in cell-free and cell-surface-bound fractions from healthy donors, patients with breast cancer, and patients with breast fibroadenoma. Tumour development was shown to lead to significant changes in the distribution of cirDNA between cell-free and cell-surface-bound fractions. Analysis of RARbeta2 and RASSF1A methylation in the total cirDNA provides 95% diagnostic coverage in breast cancer patients, 60% in patients with benign lesions, and is without false-positive results in healthy women. Results of the study indicate that methylation-specific PCR of RARbeta2 and RASSF1A genes based on the total cirDNA combined with the quantitative analysis of cirDNA distribution between cell-bound and cell-free fractions in blood provide the sensitive and accurate detection and discrimination of malignant and benign breast tumours.
肿瘤发展的特征是循环DNA(cirDNA)浓度增加以及血浆DNA中与肿瘤相关的变化。研究了健康供体、乳腺癌患者和乳腺纤维腺瘤患者的无细胞和细胞表面结合部分中cirDNA的浓度以及RARbeta2、RASSF1A和HIC-1基因启动子的甲基化情况。结果表明,肿瘤发展会导致cirDNA在无细胞和细胞表面结合部分之间的分布发生显著变化。对总cirDNA中RARbeta2和RASSF1A甲基化的分析在乳腺癌患者中提供了95%的诊断覆盖率,在良性病变患者中为60%,且在健康女性中无假阳性结果。研究结果表明,基于总cirDNA的RARbeta2和RASSF1A基因甲基化特异性PCR结合血液中细胞结合和无细胞部分之间cirDNA分布的定量分析,能够敏感且准确地检测和区分恶性和良性乳腺肿瘤。