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Status |
Public on Apr 23, 2021 |
Title |
Genome-wide DNA methylation maps of Decitabine and/or Cisplatin treated bladder cancer cells. |
Organism |
Homo sapiens |
Experiment type |
Methylation profiling by high throughput sequencing
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Summary |
It is well established that low-dose Decitabine treatment can sustain long-term antitumor effects by targeting DNA methylation and altering gene expression32. We performed methylated DNA immunoprecipitation (MEDIP) followed by next-generation sequencing in 5637 cells. Daily Decitabine treatment with 100 nM for 72 hr (with or without 100ng/ml cisplatin treatment) reduced the methylation level at CpG-islands in the genome of 5637 cells . However, this low-dose DEC treatment did not cause a significant reduction of DNA methylation in non-CpG islands regions.Our study represents the first detailed analysis of DNA methylome generated by RNA-seq technology in bladder cancer cells treated with low-dose decitabine. This study help to reveal the direct target genes of decitabine in bladder cancer treatement.
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Overall design |
Examination of DNA methylation level of bladder cancer cells treated with lose-dose decitabine.
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Contributor(s) |
Li Y, Li J |
Citation missing |
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Submission date |
Apr 23, 2018 |
Last update date |
Apr 24, 2021 |
Contact name |
Jiong Li |
E-mail(s) |
[email protected]
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Phone |
3105617186
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Organization name |
UCLA
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Department |
School of Dentistry
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Lab |
Cunyu Wang
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Street address |
33-030 CHS
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City |
Los Angeles |
State/province |
CA - California |
ZIP/Postal code |
91406 |
Country |
USA |
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Platforms (1) |
GPL21290 |
Illumina HiSeq 3000 (Homo sapiens) |
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Samples (6)
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Relations |
BioProject |
PRJNA451473 |
SRA |
SRP142314 |