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Status |
Public on Dec 18, 2019 |
Title |
DNA methylation instability by BRAF-mediated TET silencing and lifestyle-exposure divides colon cancer pathways [Colo320 cell line] |
Organism |
Homo sapiens |
Experiment type |
Methylation profiling by genome tiling array
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Summary |
Promoter hypermethylation divides colon cancers into subtypes with and without a CpG island methylator phenotype (CIMP). Here, we performed genome-wide DNA methylation profiling of colonic normal and tumor tissues to dissect development of CpG hypermethylation in colon carcinogenesis. This identified age-environment related versus genetically driven CpG hypermethylation, the latter being associated with CIMP cancers. We found a strong association between BRAFV600E mutation and downregulation of the DNA demethylases TET1 and TET2. Expression of BRAFV600E in CIMP cancer cells suppressed TET1 transcription, which was sufficient to establish hypermethylation at CIMP genes promoters, including that of TET2. This phenotype was reverted by the BRAFV600E inhibitor vemurafenib. Thus, BRAFV600E, via impairment of cytosine de-methylation, is a genetic driver of CIMP in colon tumorigenesis.
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Overall design |
Colo320 cells stably expressing oncogenic BRAF (BRAFV600E) or GFP. Bisulfite-converted DNA were hybridised to the Illumina HumanMethylation850 BeadChip (EPIC array)
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Contributor(s) |
Noreen F, Truninger K, Schär P |
Citation(s) |
31842975 |
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Submission date |
Jan 10, 2019 |
Last update date |
Jan 08, 2020 |
Contact name |
Faiza Noreen |
E-mail(s) |
[email protected]
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Organization name |
University of Basel
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Department |
Department of Biomedicine
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Street address |
Mattenstrasse 28
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City |
Basel |
ZIP/Postal code |
4058 |
Country |
Switzerland |
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Platforms (1) |
GPL23976 |
Illumina Infinium HumanMethylation850 BeadChip |
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Samples (4)
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This SubSeries is part of SuperSeries: |
GSE98534 |
DNA methylation instability by BRAF-mediated TET silencing and lifestyle-exposure divides colon cancer pathways |
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Relations |
BioProject |
PRJNA514303 |