Integrated Methylation and Copy Number Analysis for Noninvasive Bladder Cancer Detection in Urine
Irene J. Beijert, Birgit M.M. Wever, Norbert Moldovan, Yara van den Burgt, Annick Nouwens, Ymke van der Pol, Anouk E. Hentschel, Judith Bosschieter, Birgit Lissenberg-Witte, Paul C. Kauer, R. Jeroen A. van Moorselaar, Florent Mouliere, Jakko A. Nieuwenhuijzen, Renske D.M. SteenbergenPURPOSE
The molecular analysis of urine cell-free DNA offers a noninvasive tool to advanced bladder cancer (BC) management. Assessment of somatic copy number aberration (SCNA) and DNA methylation analysis have emerged as promising approaches for BC detection. Here, we developed an integrated analysis to assess both SCNA and targeted methylation changes from the same template molecules, which we named the integrated sequencing-based copy number and methylation analysis in urine (iSECURE) method.
MATERIALS AND METHODS
Urine samples of 30 patients with primary BC, 28 patients with recurrent BC, and 31 hematuria controls were collected at home. Copy number profiling and tumor fraction (TF) estimation were performed by shallow whole-genome enzymatic methyl sequencing. Methylation sequencing libraries were also used for the measurement of a previously validated three-gene methylation marker panel (
RESULTS
TF and methylation levels were significantly higher in patients with BC compared with controls (
CONCLUSION
We developed a single workflow for copy number profiling and targeted methylation analysis, requiring less input DNA and hands-on time. The high accuracy of iSECURE in home-collected urine samples for detecting both primary and recurrent BC underscores its clinical potential.