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开发基于 DNA 甲基化的前列腺癌血液检测并初步临床关联分析

Development and initial clinical correlation of a DNA methylation-based blood test for prostate cancer.

机构信息

Department of Medicine, McMaster University, Hamilton, Ontario, Canada.

Department of Urology, Queen's University, Kingston, Ontario, Canada.

出版信息

Prostate. 2020 Sep;80(12):1038-1042. doi: 10.1002/pros.24025. Epub 2020 Jun 7.

Abstract

BACKGROUND

One of the principle limitations for more precise management of advanced prostate cancer is the lack of accurate biomarkers allowing estimation of tumor burden, ongoing assessment of progression, and response to treatment. Although prostate-specific antigen (PSA) performs modestly, nonsecreting cancers including those with early castrate-resistance warrant investigation of other predictive biomarkers. The objectives of these studies were to develop and perform initial validation of a circulating tumor DNA (ctDNA) methylation assay.

METHODS

Methylation DETection of Circulating Tumor DNA (mDETECT) is a highly multiplexed targeted sequencing DNA methylation-based ctDNA blood test that captures the vast majority of prostate cancer phenotypes due to a careful development process that ensures that each probe region is methylated in at least 50% of all methylation-based subtypes and is not methylated in normal tissues. Next-generation sequencing of targeted polymerase chain reaction (PCR) products whose amplification is biased towards methylated DNA ensures the specificity of the assay by identifying multiple tumor-specific methylated CpG residues in each read.

RESULTS

The final test is comprised of 46 PCR probes to 40 regions. It is relatively resistant to contaminating normal DNA and as a result functions in both serum and plasma samples. The assay was initially validated in a variety of prostate cancer cell lines to ensure specificity. Using a small number of longitudinal samples from prostate cancer patients initiating androgen deprivation therapy, the ability of mDETECT to track tumor burden was assessed compared with PSA. The mDETECT test signal generally paralleled that of PSA increasing and decreasing commensurate with tumor evolution in these patients. In two cases it appeared to anticipate clinical progression by a number of months compared to PSA and in a PSA nonproducing case, it was able to track tumor progression.

CONCLUSIONS

mDETECT offers a promising tool for the assessment of prostate cancer burden based on the sensitive detection of prostate-specific ctDNA and requires further validation.

摘要

背景

更精确地管理晚期前列腺癌的主要限制之一是缺乏准确的生物标志物,这些标志物可以评估肿瘤负担、持续评估进展情况以及对治疗的反应。尽管前列腺特异性抗原(PSA)的作用有限,但包括那些具有早期去势抵抗的非分泌性癌症仍需要研究其他预测性生物标志物。这些研究的目的是开发和初步验证一种循环肿瘤 DNA(ctDNA)甲基化检测方法。

方法

循环肿瘤 DNA 甲基化检测(mDETECT)是一种高度多重靶向测序 DNA 甲基化 ctDNA 血液检测,由于精心的开发过程,确保每个探针区域在至少 50%的基于甲基化的亚型中都被甲基化,并且在正常组织中不被甲基化,因此可以捕获绝大多数前列腺癌表型。对偏向于甲基化 DNA 的靶向聚合酶链反应(PCR)产物进行下一代测序,通过在每个读取中识别多个肿瘤特异性甲基化 CpG 残基,确保了该检测方法的特异性。

结果

最终的测试由 46 个针对 40 个区域的 PCR 探针组成。它相对抗污染的正常 DNA,因此在血清和血浆样本中都能发挥作用。该检测方法最初在各种前列腺癌细胞系中进行了验证,以确保其特异性。使用少数开始接受雄激素剥夺治疗的前列腺癌患者的纵向样本,评估了 mDETECT 与 PSA 相比跟踪肿瘤负担的能力。在这些患者中,mDETECT 测试信号通常与 PSA 平行增加和减少,与肿瘤演变一致。在两种情况下,与 PSA 相比,它似乎提前了几个月的临床进展,在一种 PSA 非产生的情况下,它能够跟踪肿瘤进展。

结论

mDETECT 为基于前列腺特异性 ctDNA 的灵敏检测评估前列腺癌负担提供了一种有前途的工具,需要进一步验证。

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