Gynaecological Cancer Research Group, Adult Cancer Program, Lowy Cancer Research Centre, Department of Obstetrics & Gynaecology, School of Women's and Children's Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
PLoS One. 2021 Apr 26;16(4):e0250561. doi: 10.1371/journal.pone.0250561. eCollection 2021.
Assays measuring cell-free DNA (cfDNA) in blood have widespread potential in modern medicine. However, a comprehensive understanding of cfDNA dynamics in healthy individuals is required to assist in the design of assays that maximise the signal driven by pathological changes, while excluding fluctuations that are part of healthy physiological processes. The menstrual cycle involves major remodelling of endometrial tissue and associated apoptosis, yet there has been little investigation of the impact of the menstrual cycle on cfDNA levels. Paired plasma samples were collected from 40 healthy women on menstruating (M) and non-menstruating (NM) days of their cycle. We measured total cfDNA by targeting ALU repetitive sequences and measured endothelial-derived cfDNA by methylation-specific qPCR targeting an endothelium-unique unmethylated CDH5 DNA region. CfDNA integrity and endothelial cfDNA concentration, but not total cfDNA, are consistent across time between NM and M. No significant changes in total (ALU-115 p = 0.273; ALU-247 p = 0.385) or endothelial cell specific (p = 0.301) cfDNA were observed, leading to the conclusion that menstrual status at the time of diagnostic blood collection should not have a significant impact on the quantitation of total cfDNA and methylation-based cancer assays.
检测血液中的游离 DNA(cfDNA)在现代医学中有广泛的应用潜力。然而,为了协助设计能够最大程度地利用由病理变化引起的信号,同时排除属于健康生理过程一部分的波动的检测方法,需要全面了解健康个体中 cfDNA 的动态变化。月经周期涉及子宫内膜组织的重大重塑和相关的细胞凋亡,但对月经周期对 cfDNA 水平的影响的研究甚少。从 40 名健康女性的月经(M)和非月经(NM)期间收集配对的血浆样本。我们通过靶向 ALU 重复序列测量总 cfDNA,并通过针对内皮细胞独特的未甲基化 CDH5 DNA 区域的甲基化特异性 qPCR 测量内皮细胞衍生的 cfDNA。NM 和 M 之间的 cfDNA 完整性和内皮 cfDNA 浓度,但不是总 cfDNA,在时间上是一致的。未观察到总(ALU-115 p = 0.273;ALU-247 p = 0.385)或内皮细胞特异性(p = 0.301)cfDNA 的显著变化,因此可以得出结论,在进行诊断性血液采集时的月经状态不应对总 cfDNA 和基于甲基化的癌症检测的定量检测产生重大影响。