Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/132661
Title: A new approach to epigenome-wide discovery of non-invasive methylation biomarkers for colorectal cancer screening in circulating cell-free DNA using pooled samples
Author: Gallardo Gómez, María
Moran, Sebastian
Páez de la Cadena, María
Martínez Zorzano, Vicenta Soledad
Rodríguez Berrocal, Francisco Javier
Rodríguez Girondo, Mar
Esteller, Manel
Cubiella, Joaquín
Bujanda, Luis
Castells Garangou, Antoni
Balaguer, Francesc
Jover, Rodrigo
Chiara, Loretta de
Keywords: Càncer colorectal
Epigenètica
ADN
Metilació
Marcadors bioquímics
Colorectal cancer
Epigenetics
DNA
Methylation
Biochemical markers
Issue Date: 15-Apr-2018
Publisher: BioMed Central
Abstract: BACKGROUND: Colorectal cancer is the fourth cause of cancer-related deaths worldwide, though detection at early stages associates with good prognosis. Thus, there is a clear demand for novel non-invasive tests for the early detection of colorectal cancer and premalignant advanced adenomas, to be used in population-wide screening programs. Aberrant DNA methylation detected in liquid biopsies, such as serum circulating cell-free DNA (cfDNA), is a promising source of non-invasive biomarkers. This study aimed to assess the feasibility of using cfDNA pooled samples to identify potential serum methylation biomarkers for the detection of advanced colorectal neoplasia (colorectal cancer or advanced adenomas) using microarray-based technology. RESULTS: cfDNA was extracted from serum samples from 20 individuals with no colorectal findings, 20 patients with advanced adenomas, and 20 patients with colorectal cancer (stages I and II). Two pooled samples were prepared for each pathological group using equal amounts of cfDNA from 10 individuals, sex-, age-, and recruitment hospital-matched. We measured the methylation levels of 866,836 CpG positions across the genome using the MethylationEPIC array. Pooled serum cfDNA methylation data meets the quality requirements. The proportion of detected CpG in all pools (> 99% with detection p value < 0.01) exceeded Illumina Infinium methylation data quality metrics of the number of sites detected. The differential methylation analysis revealed 1384 CpG sites (5% false discovery rate) with at least 10% difference in the methylation level between no colorectal findings controls and advanced neoplasia, the majority of which were hypomethylated. Unsupervised clustering showed that cfDNA methylation patterns can distinguish advanced neoplasia from healthy controls, as well as separate tumor tissue from healthy mucosa in an independent dataset. We also observed that advanced adenomas and stage I/II colorectal cancer methylation profiles, grouped as advanced neoplasia, are largely homogenous and clustered close together. CONCLUSIONS: This preliminary study shows the viability of microarray-based methylation biomarker discovery using pooled serum cfDNA samples as an alternative approach to tissue specimens. Our strategy sets an open door for deciphering new non-invasive biomarkers not only for colorectal cancer detection, but also for other types of cancers.
Note: Reproducció del document publicat a: https://doi.org/10.1186/s13148-018-0487
It is part of: Clinical Epigenetics, 2018, vol. 2018, num. 10, p. 53
URI: http://hdl.handle.net/2445/132661
Related resource: https://doi.org/10.1186/s13148-018-0487
ISSN: 1868-7075
Appears in Collections:Articles publicats en revistes (Ciències Fisiològiques)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)

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