374份循环DNA样本的回顾性分析作为支持实体肿瘤多靶向表观遗传治疗(MTET)临床管理的生物标志物分析

M. Nezami, C. Klowsowski, Hager Sj
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引用次数: 0

摘要

在这篇摘要中,我们回顾性回顾了从173名接受多靶向表观遗传治疗(MTET)的患者中提取的374份循环dna样本的初步结果,MTET是天然组蛋白去乙酰化酶抑制剂和DNMT甲基转移酶抑制剂的组合。在体外和体内模型中,这种疗法可以动态地中断各种实体肿瘤类型中改变基因的表达。我们假设,在这些病例中,循环DNA的连续监测为基于驱动基因的治疗决策提供了一个可行的选择。我们还能够通过监测这些患者的肿瘤循环DNA突变等位基因片段来跟踪他们的抗肿瘤反应,并提出了与中期表观遗传治疗效果的直接关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Retrospective Review of 374 Samples, Circulating DNA; as a Biomarker Assay to Support Clinical Management in Solid Tumors Treated With Multi Targeted Epigenetic Therapy (MTET)
Here in this abstract we retrospectively review preliminary findings on 374 samples of circulating DNAextracted from 173 patients treated by multitargeted epigenetic therapy (MTET), which is a combination of natural histone deacetylase inhibitors and DNMT methyl transferase inhibitors. This therapy could dynamically interrupt the expression of altered genes, in a variety of solid tumor types, both in invitro and invivo models. We hypothesize that serial monitoring of the circulating DNA provides a feasible option for therapeutic decisions making based on presence of the driver genes in these cases. We also were able to track the antineoplastic response in these group of patients by monitoring their tumor circulating DNA mutated allele fractions and propose a direct correlation with interim epigenetic therapy effectiveness.
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