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Series GSE174625 Query DataSets for GSE174625
Status Public on May 19, 2021
Title Whole-genome methylation study of congenital lung malformations in children
Organism Homo sapiens
Experiment type Methylation profiling by genome tiling array
Summary The treatment of asymptomatic patients with congenital pulmonary malformations (CPMs) remains controversial, partially because the relationship between congenital lung malformations and malignancy is still undefined. Change in methylation pattern is a crucial event in human cancer, including lung cancer. We therefore studied all differentially methylated regions (DMRs) in a series of CPMs in an attempt to find methylation anomalies in genes already described in association with malignancy. The DNA extracted from resected congenital lung malformations and control lung tissue was screened using Illumina MethylationEPIC arrays. Comparison between the group of malformed samples or the malformed samples of same histology or each malformed sample and the controls, and between a pleuropulmonary blastoma (PPB) and controls were performed. All differentially methylated regions (DMRs) with an adjusted p value < 0,05 were studied. Every comparison highlighted a number of DMRs closed to genes involved either in cell proliferation or in embryonic development or included in the Cancer Gene Census. Their abnormal methylation had been already described in lung tumors. The presence of methylation abnormalities is suggestive of a correlation between congenital lung malformations and some step of malignant transformation.
 
Overall design 29 total fresh-frozen paediatric lung samples: 8 healthy lung tissues, 1 Pleuropulmonary Blastoma sample, 20 Congenital Pulmonary Malformation tissues
 
Contributor(s) Patrizi S, Pederiva F, d'Adamo AP
Citation(s) 34262872
Submission date May 18, 2021
Last update date Aug 18, 2021
Contact name Sara Patrizi
E-mail(s) sara.patrizi94@gmail.com
Organization name University of Trieste
Street address via dell'Istria 65
City Trieste
ZIP/Postal code 34137
Country Italy
 
Platforms (1)
GPL21145 Infinium MethylationEPIC
Samples (29)
GSM5320711 Congenital Pulmonary Malformation, patient 1
GSM5320712 Congenital Pulmonary Malformation, patient 2
GSM5320713 Congenital Pulmonary Malformation, patient 3
Relations
BioProject PRJNA730816

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE174625_RAW.tar 574.8 Mb (http)(custom) TAR (of IDAT)
GSE174625_matrix_processed.txt.gz 169.5 Mb (ftp)(http) TXT
GSE174625_matrix_signal_intensities.txt.gz 126.4 Mb (ftp)(http) TXT
Processed data are available on Series record

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