4.6 Article

Longitudinal analysis of individual cfDNA methylome patterns in metastatic prostate cancer

期刊

CLINICAL EPIGENETICS
卷 13, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13148-021-01155-w

关键词

Metastatic prostate cancer; DNA methylation; Longitudinal study; cfDNA; Liquid biopsy

资金

  1. Movember [PCT13MCD, CRS17SIL]
  2. Science Foundation Ireland under the Investigator Programme OPTi-PREDICT [15/IA/3104]
  3. Strategic Research Programme Precision Oncology Ireland [18/SPP/3522]
  4. Irish Cancer Society

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This study investigated the dynamics of personal DNA methylomic profiles of metastatic prostate cancer patients during disease progression and therapy administration. Longitudinal assessment of cfDNA methylation revealed dynamic patterns associated with disease progression and therapy administration, highlighting the potential of using liquid biopsies to study prostate cancer evolution at a methylomic level.
Background: Disease progression and therapeutic resistance are hallmarks of advanced stage prostate cancer (PCa), which remains a major cause of cancer-related mortality around the world. Longitudinal studies, coupled with the use of liquid biopsies, offer a potentially new and minimally invasive platform to study the dynamics of tumour progression. Our aim was to investigate the dynamics of personal DNA methylomic profiles of metastatic PCa (mPCa) patients, during disease progression and therapy administration. Results: Forty-eight plasma samples from 9 mPCa patients were collected, longitudinally, over 13-21 months. After circulating cell-free DNA (cfDNA) isolation, DNA methylation was profiled using the Infinium MethylationEPIC BeadChip. The top 5% most variable probes across time, within each individual, were utilised to study dynamic methylation patterns during disease progression and therapeutic response. Statistical testing was carried out to identify differentially methylated genes (DMGs) in cfDNA, which were subsequently validated in two independent mPCa (cfDNA and FFPE tissue) cohorts. Individual cfDNA global methylation patterns were temporally stable throughout the disease course. However, a proportion of CpG sites presented a dynamic temporal pattern that was consistent with clinical events, including different therapies, and were prominently associated with genes linked to immune response pathways. Additionally, study of the tumour fraction of cfDNA identified > 2000 DMGs with dynamic methylation patterns. Conclusions: Longitudinal assessment of cfDNA methylation in mPCa patients unveiled dynamic patterns associated with disease progression and therapy administration, thus highlighting the potential of using liquid biopsies to study PCa evolution at a methylomic level.

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