Cluster analysis of genomic ETV6-RUNX1 (TEL-AML1) fusion sites in childhood acute lymphoblastic leukemia

H. von Goessel; U. Jacobs; S. Semper; M. Krumbholz; T. Langer; T. Keller; A. Schrauder; V. H.J. van der Velden; J. J.M. van Dongen; J. Harbott; E. R. Panzer-Grümayer; M. Schrappe; W. Rascher; M. Metzler

doi:10.1016/j.leukres.2008.11.001

Cluster analysis of genomic ETV6-RUNX1 (TEL-AML1) fusion sites in childhood acute lymphoblastic leukemia

H. von Goessel, U. Jacobs, S. Semper, M. Krumbholz, T. Langer, T. Keller, A. Schrauder, V. H.J. van der Velden, J. J.M. van Dongen, J. Harbott, E. R. Panzer-Grümayer, M. Schrappe, W. Rascher, M. Metzler^*

^*Korrespondierende/r Autor/-in für diese Arbeit

Klinik für Kinder- und Jugendmedizin

22 Zitate (Scopus)

Abstract

Fusion between ETV6 and RUNX1 defines the largest genetic subgroup in childhood ALL. The genomic fusion site, unique to individual patients and specific for the malignant clone, represents an ideal molecular marker for quantification of minimal residual disease. Sequencing of DNA breakpoints has been difficult due to the extended size of the respective breakpoint cluster regions. We therefore evaluated a specially designed multiplex long-range PCR assay in 65 diagnostic bone marrow samples for its suitability in routine use. Resulting fusion sites and breakpoints derived from previous studies were subject to cluster analysis to identify potential sequence motifs involved in translocation initiation.

Originalsprache	Englisch
Zeitschrift	Leukemia Research
Jahrgang	33
Ausgabenummer	8
Seiten (von - bis)	1082-1088
Seitenumfang	7
ISSN	0145-2126
DOIs	https://doi.org/10.1016/j.leukres.2008.11.001
Publikationsstatus	Veröffentlicht - 08.2009

Fördermittel

This study was supported by a Wilhelm-Sander Foundation grant to MM and TL. HvG was supported by the ELAN program of the University of Erlangen. ERP-G was received grants by the ÖNB Jubilaeumsfond, FWF and GENAU-CHILD Projekt.

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Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

SDG 3 – Gesundheit und Wohlergehen

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Forschungsschwerpunkt: Gehirn, Hormone, Verhalten - Center for Brain, Behavior and Metabolism (CBBM)

Dokumente

10.1016/j.leukres.2008.11.001

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von Goessel, H., Jacobs, U., Semper, S., Krumbholz, M., Langer, T., Keller, T., Schrauder, A., van der Velden, V. H. J., van Dongen, J. J. M., Harbott, J., Panzer-Grümayer, E. R., Schrappe, M., Rascher, W., & Metzler, M. (2009). Cluster analysis of genomic ETV6-RUNX1 (TEL-AML1) fusion sites in childhood acute lymphoblastic leukemia. Leukemia Research, 33(8), 1082-1088. https://doi.org/10.1016/j.leukres.2008.11.001

@article{dc7a83b8eaf4485ca766a6ee2d3301fb,

title = "Cluster analysis of genomic ETV6-RUNX1 (TEL-AML1) fusion sites in childhood acute lymphoblastic leukemia",

abstract = "Fusion between ETV6 and RUNX1 defines the largest genetic subgroup in childhood ALL. The genomic fusion site, unique to individual patients and specific for the malignant clone, represents an ideal molecular marker for quantification of minimal residual disease. Sequencing of DNA breakpoints has been difficult due to the extended size of the respective breakpoint cluster regions. We therefore evaluated a specially designed multiplex long-range PCR assay in 65 diagnostic bone marrow samples for its suitability in routine use. Resulting fusion sites and breakpoints derived from previous studies were subject to cluster analysis to identify potential sequence motifs involved in translocation initiation.",

author = "\{von Goessel\}, H. and U. Jacobs and S. Semper and M. Krumbholz and T. Langer and T. Keller and A. Schrauder and \{van der Velden\}, \{V. H.J.\} and \{van Dongen\}, \{J. J.M.\} and J. Harbott and Panzer-Gr{\"u}mayer, \{E. R.\} and M. Schrappe and W. Rascher and M. Metzler",

note = "Funding Information: This study was supported by a Wilhelm-Sander Foundation grant to MM and TL. HvG was supported by the ELAN program of the University of Erlangen. ERP-G was received grants by the {\"O}NB Jubilaeumsfond, FWF and GENAU-CHILD Projekt. Copyright: Copyright 2009 Elsevier B.V., All rights reserved.",

year = "2009",

month = aug,

doi = "10.1016/j.leukres.2008.11.001",

language = "English",

volume = "33",

pages = "1082--1088",

journal = "Leukemia Research",

issn = "0145-2126",

publisher = "Elsevier Ltd",

number = "8",

}

von Goessel, H, Jacobs, U, Semper, S, Krumbholz, M, Langer, T, Keller, T, Schrauder, A, van der Velden, VHJ, van Dongen, JJM, Harbott, J, Panzer-Grümayer, ER, Schrappe, M, Rascher, W & Metzler, M 2009, 'Cluster analysis of genomic ETV6-RUNX1 (TEL-AML1) fusion sites in childhood acute lymphoblastic leukemia', Leukemia Research, Jg. 33, Nr. 8, S. 1082-1088. https://doi.org/10.1016/j.leukres.2008.11.001

TY - JOUR

T1 - Cluster analysis of genomic ETV6-RUNX1 (TEL-AML1) fusion sites in childhood acute lymphoblastic leukemia

AU - von Goessel, H.

AU - Jacobs, U.

AU - Semper, S.

AU - Krumbholz, M.

AU - Langer, T.

AU - Keller, T.

AU - Schrauder, A.

AU - van der Velden, V. H.J.

AU - van Dongen, J. J.M.

AU - Harbott, J.

AU - Panzer-Grümayer, E. R.

AU - Schrappe, M.

AU - Rascher, W.

AU - Metzler, M.

N1 - Funding Information: This study was supported by a Wilhelm-Sander Foundation grant to MM and TL. HvG was supported by the ELAN program of the University of Erlangen. ERP-G was received grants by the ÖNB Jubilaeumsfond, FWF and GENAU-CHILD Projekt. Copyright: Copyright 2009 Elsevier B.V., All rights reserved.

PY - 2009/8

Y1 - 2009/8

N2 - Fusion between ETV6 and RUNX1 defines the largest genetic subgroup in childhood ALL. The genomic fusion site, unique to individual patients and specific for the malignant clone, represents an ideal molecular marker for quantification of minimal residual disease. Sequencing of DNA breakpoints has been difficult due to the extended size of the respective breakpoint cluster regions. We therefore evaluated a specially designed multiplex long-range PCR assay in 65 diagnostic bone marrow samples for its suitability in routine use. Resulting fusion sites and breakpoints derived from previous studies were subject to cluster analysis to identify potential sequence motifs involved in translocation initiation.

AB - Fusion between ETV6 and RUNX1 defines the largest genetic subgroup in childhood ALL. The genomic fusion site, unique to individual patients and specific for the malignant clone, represents an ideal molecular marker for quantification of minimal residual disease. Sequencing of DNA breakpoints has been difficult due to the extended size of the respective breakpoint cluster regions. We therefore evaluated a specially designed multiplex long-range PCR assay in 65 diagnostic bone marrow samples for its suitability in routine use. Resulting fusion sites and breakpoints derived from previous studies were subject to cluster analysis to identify potential sequence motifs involved in translocation initiation.

UR - https://www.scopus.com/pages/publications/67349202133

U2 - 10.1016/j.leukres.2008.11.001

DO - 10.1016/j.leukres.2008.11.001

M3 - Journal articles

C2 - 19081626

AN - SCOPUS:67349202133

SN - 0145-2126

VL - 33

SP - 1082

EP - 1088

JO - Leukemia Research

JF - Leukemia Research

IS - 8

ER -

Cluster analysis of genomic ETV6-RUNX1 (TEL-AML1) fusion sites in childhood acute lymphoblastic leukemia

Abstract

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UN SDGs

Strategische Forschungsbereiche und Zentren

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