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pmid:33105711

Comprehensive Analysis of DNA Methylation and Prediction of Response to NeoadjuvantTherapy in Locally Advanced Rectal Cancer.

Luisa Matos do Canto · Mateus Camargo Barros-Filho · Cláudia Aparecida Rainho · Diogo Marinho · Bruna Elisa Catin Kupper · Maria Dirlei Ferreira de Souza Begnami · Cristovam Scapulatempo-Neto · Birgitte Mayland Havelund · Jan Lindebjerg · Fabio Albuquerque Marchi · Jan Baumbach · Samuel Aguiar · Silvia Regina Rogatto

Cancers · 2020 doi:10.3390/cancers12113079

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Comprehensive Analysis of DNA Methylation and Prediction of Response to NeoadjuvantTherapy in Locally Advanced Rectal Cancer.
doi
10.3390/cancers12113079
pmid
33105711
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Luisa Matos do Canto
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Mateus Camargo Barros-Filho
[2]
Cláudia Aparecida Rainho
[3]
Diogo Marinho
[4]
Bruna Elisa Catin Kupper
[5]
Maria Dirlei Ferreira de Souza Begnami
[6]
Cristovam Scapulatempo-Neto
[7]
Birgitte Mayland Havelund
[8]
Jan Lindebjerg
[9]
Fabio Albuquerque Marchi
[10]
Jan Baumbach
[11]
Samuel Aguiar
[12]
Silvia Regina Rogatto
journal
Cancers
year
2020
abstract
The treatment for locally advanced rectal carcinomas (LARC) is based on neoadjuvant chemoradiotherapy (nCRT) and surgery, which results in pathological complete response (pCR) in up to 30% of patients. Since epigenetic changes may influence response to therapy, we aimed to identify DNA methylation markers predictive of pCR in LARC patients treated with nCRT. We used high-throughput DNA methylation analysis of 32 treatment-naïve LARC biopsies and five normal rectal tissues to explore the predictive value of differentially methylated (DM) CpGs. External validation was carried out with The Cancer Genome Atlas-Rectal Adenocarcinoma (TCGA-READ 99 cases). A classifier based on three-CpGs DM (linked to OBSL1, GPR1, and INSIG1 genes) was able to discriminate pCR from incomplete responders with high sensitivity and specificity. The methylation levels of the selected CpGs confirmed the predictive value of our classifier in 77 LARCs evaluated by bisulfite pyrosequencing. Evaluation of external datasets (TCGA-READ, GSE81006, GSE75546, and GSE39958) reproduced our results. As the three CpGs were mapped near to regulatory elements, we performed an integrative analysis in regions associated with predicted cis-regulatory elements. A positive and inverse correlation between DNA methylation and gene expression was found in two CpGs. We propose a novel predictive tool based on three CpGs potentially useful for pretreatment screening of LARC patients and guide the selection of treatment modality.
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Clinical and histopathological features of locally advanced rectal cancer patients included in this study.
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candidate
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pearson_r
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tier
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capability:computational_analysis
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GSE132668
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GSE39958
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GSE132668
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GSE75546
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GSE39958
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GSE81006
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The large-scale methylation data is available at the Gene Expression Omnibus database (GSE132668 https://www.ncbi.nlm.nih.gov/geo/). The original data can also be obtained from the authors upon request.
basis
The paper names GSE132668, GSE75546, GSE39958, GSE81006, GSE123390 in Gene Expression Omnibus and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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pearson_r
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MiniMax-M3.1-Flash
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minimax
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source:pmid:33105711
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manuscript
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PMID 33105711 full text
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data:geo:GSE123390
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GEO GSE123390
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data:geo:GSE123390
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[8]
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e of our classifier in 77 LARCs evaluated by bisulfite pyrosequencing. Evaluation of external datas
[1]
es (limma p < 0.001; FDR < 5%; |Δβ| > 0.15) (EPIC BeadChip platform, Illumina), Table S2: Cand
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cg01072658 probe, Infinium Human Methylation 450k BeadChip platform, Illumina) in rectal cance
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Complete file
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