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Verfasst von:Braczynski, Anne Kristin [VerfasserIn]   i
 Capper, David [VerfasserIn]   i
 Jones, David T. W. [VerfasserIn]   i
 Schittenhelm, Jens Florian [VerfasserIn]   i
 Stichel, Damian [VerfasserIn]   i
 Deimling, Andreas von [VerfasserIn]   i
 Harter, Patrick Nikolaus [VerfasserIn]   i
 Mittelbronn, Michel Guy André [VerfasserIn]   i
Titel:High density DNA methylation array is a reliable alternative for PCR-based analysis of the MGMT promoter methylation status in glioblastoma
Verf.angabe:Anne K. Braczynski, David Capper, David T.W. Jones, Jens Schittenhelm, Damian Stichel, Andreas von Deimling, Patrick N. Harter, Michel Mittelbronn
Jahr:2020
Jahr des Originals:2019
Umfang:7 S.
Fussnoten:Available online 11 November 2019 ; Gesehen am 23.04.2020
Titel Quelle:Enthalten in: Pathology, research and practice
Ort Quelle:München : Elsevier, 1978
Jahr Quelle:2020
Band/Heft Quelle:216(2020,1) Artikel-Nummer 152728, 7 Seiten
ISSN Quelle:1618-0631
Abstract:Aim - MGMT promoter methylation status is an important biomarker predicting survival and response to chemotherapy in patients suffering from glioblastoma. Since new diagnostic methods such as methylome-based classification of brain tumors are more and more frequently performed, we aimed at comparing the suitability of calculating the MGMT promoter methylation status in a quantitative manner from the methylome profiling as compared to the classic gold standard assessment by PCR. - Methods - Our cohort consisted of 39 cases diagnosed as “glioblastoma, IDH-wildtype” of which the MGMT promoter methylation status was analyzed with both methylation-specific PCR and high density DNA methylation array using the STP-27 algorithm. Contradictory results were validated by pyrosequencing. - Results - The inter-method reliability reached 77% (kappa-coefficient: 0.58) when also cases with an inconclusive result in one or the other method were taken into account. When only cases with conclusive results in both methods were considered, a very high inter-method reliability of 91% (kappa-coefficient: 0.86) could be achieved. For “methylated” cases, no contradictory results were obtained. For the remaining two cases with discrepant results subsequent pyrosequencing analyses spoke in favor of each previously applied method once. - Conclusion - In addition to its benefits for molecular subgrouping and copy number analysis of brain tumors, DNA-methylation based classification is a highly reliable tool for the assessment of MGMT promoter methylation status in glioblastoma patients.
DOI:doi:10.1016/j.prp.2019.152728
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1016/j.prp.2019.152728
 Volltext: http://www.sciencedirect.com/science/article/pii/S0344033819317455
 DOI: https://doi.org/10.1016/j.prp.2019.152728
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Glioblastoma
 Glioma
 High density DNA methylation array
 Illumina methylome bead chip array
 MGMT promoter methylation
 MS-PCR
K10plus-PPN:1695827120
Verknüpfungen:→ Zeitschrift

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