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pmid:33466447
Novel Epigenetic Eight-Gene Signature Predictive of Poor Prognosis and MSI-Like Phenotype in Human Metastatic Colorectal Carcinomas.
Valentina Condelli · Giovanni Calice · Alessandra Cassano · Michele Basso · Maria Grazia Rodriquenz · Angela Zupa · Francesca Maddalena · Fabiana Crispo · Michele Pietrafesa · Michele Aieta · Alessandro Sgambato · Giampaolo Tortora · Pietro Zoppoli · Matteo Landriscina
Cancers · 2021 doi:10.3390/cancers13010158
Paper
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Experiment
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Data
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Analysis
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Execution
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Complete file
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This study addressed the hypothesis that the DNA methylation profiling may predict the clinical behavior of metastatic CRCs (mCRCs). The global methylation profile of two human mCRC subgroups with significantly different outcome was analyzed and compared with gene expression and methylation data from The Cancer Genome Atlas COlon ADenocarcinoma (TCGA COAD) and the NCBI GENE expression Omnibus repository (GEO) GSE48684 mCRCs datasets to identify a prognostic signature of functionally methylated genes. A novel epigenetic signature of eight hypermethylated genes was characterized that was able to identify mCRCs with poor prognosis, which had a CpG-island methylator phenotype (CIMP)-high and microsatellite instability (MSI)-like phenotype. Interestingly, methylation events were enriched in genes located on the q-arm of chromosomes 13 and 20, two chromosomal regions with gain/loss alterations associated with adenoma-to-carcinoma progression. 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