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醋酸阿比特龙治疗的前列腺癌患者的无细胞 DNA 修饰动力学。

Cell-Free DNA Modification Dynamics in Abiraterone Acetate-Treated Prostate Cancer Patients.

机构信息

Institute of Biotechnology, Life Sciences Center, Vilnius University, Vilnius, Lithuania.

The Krembil Family Epigenetics Laboratory, The Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.

出版信息

Clin Cancer Res. 2018 Jul 15;24(14):3317-3324. doi: 10.1158/1078-0432.CCR-18-0101. Epub 2018 Apr 3.

Abstract

Primary resistance to abiraterone acetate (AA), a key medication for the treatment of metastatic castration-resistant prostate cancer, occurs in 20% to 40% of patients. We aim to identify predictive biomarkers for AA-treatment response and understand the mechanisms related to treatment resistance. We used the Infinium Human Methylation 450K BeadChip to monitor modification profiles of cell-free circulating DNA (cfDNA) in 108 plasma samples collected from 33 AA-treated patients. Thirty cytosines showed significant modification differences (FDR Q < 0.05) between AA-sensitive and AA-resistant patients during the treatment, of which 21 cytosines were differentially modified prior to treatment. In addition, AA-sensitive patients, but not AA-resistant patients, lost interindividual variation of cfDNA modification shortly after starting AA treatment, but such variation returned to initial levels in the later phases of treatment. Our findings provide a list of potential biomarkers for predicting AA-treatment response, highlight the prognostic value of using cytosine modification variance as biomarkers, and shed new insights into the mechanisms of prostate cancer relapse in AA-sensitive patients. .

摘要

原发性对醋酸阿比特龙(AA)的耐药性,AA 是治疗转移性去势抵抗性前列腺癌的关键药物,在 20%至 40%的患者中发生。我们旨在确定预测 AA 治疗反应的生物标志物,并了解与治疗耐药性相关的机制。我们使用 Infinium Human Methylation 450K BeadChip 监测了 33 名 AA 治疗患者的 108 个血浆样本中的游离循环 DNA(cfDNA)的修饰谱。在治疗过程中,30 个胞嘧啶在 AA 敏感和 AA 耐药患者之间表现出显著的修饰差异(FDR Q < 0.05),其中 21 个胞嘧啶在治疗前表现出不同的修饰。此外,AA 敏感患者,但不是 AA 耐药患者,在开始 AA 治疗后不久就失去了 cfDNA 修饰的个体间变异,但这种变异在治疗后期又恢复到初始水平。我们的研究结果提供了一组预测 AA 治疗反应的潜在生物标志物,强调了使用胞嘧啶修饰方差作为生物标志物的预后价值,并为 AA 敏感患者前列腺癌复发的机制提供了新的见解。

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