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1000 Titel
  • The number of methylated CpG sites within the MGMT promoter region linearly correlates with outcome in glioblastoma receiving alkylating agents
1000 Autor/in
  1. Siller, Sebastian |
  2. Lauseker, Michael |
  3. Karschnia, Philipp |
  4. Niyazi, Maximilian |
  5. Eigenbrod, Sabina |
  6. Giese, Armin |
  7. Tonn, Joerg-Christian |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-03-04
1000 Erschienen in
1000 Quellenangabe
  • 9(1):35
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s40478-021-01134-5 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934240/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • MGMT-promoter methylation is associated with favorable outcome in glioblastoma. The aim of this study was to determine whether the absolute number of methylated Cytosine-Guanine-dinucleotide-(CpG-)sites within the DMR-2 island of the MGMT-promoter may correlate with outcome in a qualitative or quantitative fashion. In a cohort of newly diagnosed glioblastoma patients treated with stereotactic biopsy or open tumor resection plus concomitant chemoradiotherapy, we assessed MGMT-promoter methylation by methylation-specific polymerase-chain-reaction (MSP). Methylation of the CpG-sites 74-98 within the MGMT-promoter region was additionally analysed by Sanger sequencing, and the total number of methylated CpG-sites was correlated with outcome using proportional hazards models. 215 patients with glioblastoma were identified and stratified per MSP (positive: 53%, negative: 47%). Among MSP-positive tumors, hierarchical clustering identified three subgroups with different methylation rates (median: 80% vs. 52% vs. 47%), indicating a site-dependent methylation propagation. The methylation status of a given CpG-site indicated a neighborhood-dependent methylation propagation. Survival was linearly associated with the cumulative number of methylated CpG-sites. This was particularly true in patients who received at least one adjuvant cycle of temozolomide. Notably, all CpG-sites analyzed contributed similarly to effect size; this enabled a further predictive substratification of MSP-positive tumors with median OS ranging from as low as 17.1 months (< 18 methylated CpG-sites) to as high as 26.2 months (≥ 18 methylated CpG-sites) in the overall cohort. All in all, total number of methylated CpG-sites may correlate with outcome in a linear fashion. Such analysis may therefore add further predictive value to conventional methods of determining the MGMT-promoter status.
1000 Sacherschließung
lokal Tumor Suppressor Proteins/genetics [MeSH]
lokal Aged, 80 and over [MeSH]
lokal Methylation-specific polymerase-chain-reaction
lokal Aged [MeSH]
lokal Antineoplastic Agents, Alkylating/therapeutic use [MeSH]
lokal Methylation status
lokal Cohort Studies [MeSH]
lokal Glioblastoma/drug therapy [MeSH]
lokal Male [MeSH]
lokal Base Sequence [MeSH]
lokal Glioblastoma/genetics [MeSH]
lokal Sanger sequencing
lokal Adolescent [MeSH]
lokal Female [MeSH]
lokal Brain Neoplasms/genetics [MeSH]
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal MSP
lokal Linear correlation
lokal DNA Repair Enzymes/genetics [MeSH]
lokal Survival Analysis [MeSH]
lokal Middle Aged [MeSH]
lokal Glioblastoma
lokal DNA Modification Methylases/genetics [MeSH]
lokal DNA Methylation [MeSH]
lokal Research
lokal CpG Islands [MeSH]
lokal Prognosis [MeSH]
lokal Temozolomide/therapeutic use [MeSH]
lokal Polymerase Chain Reaction/methods [MeSH]
lokal Temozolomide
lokal Promoter Regions, Genetic [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-5236-4397|https://frl.publisso.de/adhoc/uri/TGF1c2VrZXIsIE1pY2hhZWw=|https://frl.publisso.de/adhoc/uri/S2Fyc2NobmlhLCBQaGlsaXBw|https://frl.publisso.de/adhoc/uri/Tml5YXppLCBNYXhpbWlsaWFu|https://frl.publisso.de/adhoc/uri/RWlnZW5icm9kLCBTYWJpbmE=|https://frl.publisso.de/adhoc/uri/R2llc2UsIEFybWlu|https://frl.publisso.de/adhoc/uri/VG9ubiwgSm9lcmctQ2hyaXN0aWFu
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1000 Erstellt am 2023-11-16T03:54:46.656+0100
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1000 Zuletzt bearbeitet Thu Nov 30 23:57:14 CET 2023
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