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DNA-Based Assay for EPHB6 Expression in Breast Carcinoma Cells as a Potential Diagnostic Test for Detecting Tumor Cells in Circulation

机译:基于DNA的乳腺癌细胞中EPHB6表达的检测作为检测循环中肿瘤细胞的潜在诊断测试

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The early detection of breast cancer is critical for improved treatment and better management of the disease. The dissemination of tumor cells into the blood stream is known to occur early in tumor progression and these circulating tumor cells (CTCs) may be detectable before the occurrence of tumor metastasis. Methylation-specific polymerase chain reaction (MSP) can be exploited for detecting CTCs on the basis of differential methylation of numerous gene promoters in normal and carcinoma cells. In this study, we describe the relationship between loss of Ephrin receptor B6 (EPHB6) expression and the aggressiveness of breast carcinoma cell lines (BCCLs). The loss of EPHB6 expression in more aggressive BCCLs is regulated in a methylation-dependent manner. We demonstrate the ability of an EPHB6 MSP to distinguish between methylated and unmethylated EPHB6 promoters, and to predict expression of the EPHB6 transcript and protein. The sensitivity of MSP was related to the volume of blood processed for DNA isolation. As few as 50 tumor cells in 5 ml blood were detectable with a high efficiency. However, the detection of 10 tumor cells/5 ml was not as efficient. On the other hand, 5 tumor cells or 100 pg of free DNA in 200 {micro}l of blood was also easily detectable. Our results suggest that MSP could be applied to detect even a single cell in 1 ml of blood by employing appropriate modifications. The EPHB6 MSP has clinical implications for the prognosis and/or diagnosis of breast and other cancer types including neuroblastoma, melanoma, and non-small cell lung carcinoma wherein EPHB6 expression is lost in more aggressive forms of the disease.
机译:早期发现乳腺癌对于改善治疗和更好地控制疾病至关重要。已知将肿瘤细胞散布到血流中是在肿瘤进展的早期发生的,并且这些循环肿瘤细胞(CTC)在发生肿瘤转移之前可以被检测到。甲基化特异性聚合酶链反应(MSP)可以用于检测正常细胞和癌细胞中许多基因启动子的甲基化差异,从而检测CTC。在这项研究中,我们描述了Ephrin受体B6(EPHB6)表达的丧失与乳腺癌细胞系(BCCL)的侵袭性之间的关系。在更具侵略性的BCCL中,EPHB6表达的丧失以甲基化依赖性方式进行调节。我们证明了EPHB6 MSP区分甲基化和未甲基化的EPHB6启动子的能力,并预测EPHB6转录本和蛋白质的表达。 MSP的敏感性与DNA分离处理的血液量有关。高效检测到5 ml血液中只有50个肿瘤细胞。但是,检测10个肿瘤细胞/ 5 ml效率不高。另一方面,也容易检测到200微升血液中的5个肿瘤细胞或100微克游离DNA。我们的结果表明,通过采用适当的修饰,MSP还可用于检测1 ml血液中的单个细胞。 EPHB6 MSP对于乳腺癌和其他癌症类型(包括神经母细胞瘤,黑色素瘤和非小细胞肺癌)的预后和/或诊断具有临床意义,其中EPHB6表达在疾病的更具侵略性的形式中丢失。

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