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Series GSE149679 Query DataSets for GSE149679
Status Public on May 01, 2020
Title Comparative analysis of genome-wide DNA methylation identifies patterns that associate with conserved transcriptional programs in osteosarcoma
Organisms Homo sapiens; Canis lupus familiaris
Experiment type Methylation profiling by high throughput sequencing
Summary Osteosarcoma is an aggressive tumor of the bone that primarily affects young adults and adolescents. Osteosarcoma is characterized by genomic chaos and heterogeneity. While inactivation of tumor suppressor p53 TP53 is nearly universal other high frequency mutations or structural variations have not been identified. Despite this genomic heterogeneity, key conserved transcriptional programs associated with survival have been identified across human, canine and induced murine osteosarcoma. The epigenomic landscape, including DNA methylation, plays a key role in establishing transcriptional programs in all cell types. The role of epigenetic dysregulation has been studied in a variety of cancers but has yet to be explored at scale in osteosarcoma. Here we examined genome-wide DNA methylation patterns in 24 human and 44 canine osteosarcoma samples identifying groups of highly correlated DNA methylation marks in human and canine osteosarcoma samples. We also link specific DNA methylation patterns to key transcriptional programs in both human and canine osteosarcoma. Building on previous work, we built a DNA methylation-based measure for the presence and abundance of various immune cell types in osteosarcoma. Finally, we determined that the underlying state of the tumor, and not changes in cell composition, were the main driver of differences in DNA methylation across the human and canine samples. Significance: This is the first large scale study of DNA methylation in osteosarcoma and lays the ground work for the exploration of DNA methylation programs that help establish conserved transcriptional programs in the context of different genomic landscapes.
 
Overall design Targeted whole genome bisulfite sequencing of primary osteosarcoma tumors
 
Contributor(s) Mills L, Modiano J
Citation(s) 33127576
Submission date Apr 30, 2020
Last update date Feb 27, 2023
Contact name Lauren Mills
E-mail(s) ljmills@umn.edu
Phone 6126241540
Organization name University of Minnesota
Department Department of Pediatrics
Street address 420 Delaware St SE
City Minneapolis
State/province MN
ZIP/Postal code 55455
Country USA
 
Platforms (2)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
GPL16540 Illumina HiSeq 2000 (Canis lupus familiaris)
Samples (68)
GSM4508838 DOS-00
GSM4508839 DOS-02
GSM4508840 DOS-04
Relations
BioProject PRJNA629591
SRA SRP259904

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
GSE149679_130912_HG19_CpGiant_4M_EPI.bed.gz 1.8 Mb (ftp)(http) BED
GSE149679_150825_CanFam_methylome_EPI_primary_targets.bed.gz 1.9 Mb (ftp)(http) BED
GSE149679_blueprint_downloads.xlsx 10.9 Kb (ftp)(http) XLSX
GSE149679_canine_MethValues_allSamples_crossSpecies.txt.gz 4.9 Mb (ftp)(http) TXT
GSE149679_canine_moduleMembers_crossSpecies.xlsx 309.7 Kb (ftp)(http) XLSX
GSE149679_canine_module_pathway_crossSpecies.xlsx 23.1 Kb (ftp)(http) XLSX
GSE149679_canine_numberMembers_byModule.xlsx 8.4 Kb (ftp)(http) XLSX
GSE149679_diffMeth_regions_pureCellPop.xlsx 126.4 Kb (ftp)(http) XLSX
GSE149679_dogMeth_hg38coord_closest_humanMeth_hg38coord.txt.gz 2.2 Mb (ftp)(http) TXT
GSE149679_human_MethValues_allSamples_crossSpecies.txt.gz 3.4 Mb (ftp)(http) TXT
GSE149679_human_moduleMembership_crossSpecies.xlsx 771.1 Kb (ftp)(http) XLSX
GSE149679_human_module_pathway_crossSpecies.xlsx 60.3 Kb (ftp)(http) XLSX
GSE149679_human_numberMembers_byModule.xlsx 9.1 Kb (ftp)(http) XLSX
GSE149679_sorted_130912_HG19_CpGiant_4M_EPI_windowed.bed.gz 2.9 Mb (ftp)(http) BED
GSE149679_sorted_150825_CanFam_methylome_EPI_primary_targets_windowed.bed.gz 1.7 Mb (ftp)(http) BED
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Processed data are available on Series record

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