Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2.

Exome sequencing of primary tumors identifies complex somatic mutation patterns. Assignment of relevance of individual somatic mutations is difficult and poses the next challenge for interpretation of next generation sequencing data. Here we present an approach how exome sequencing in combination wi...

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Autores principales: Thorsten Klampfl, Jelena D Milosevic, Ana Puda, Andreas Schönegger, Klaudia Bagienski, Tiina Berg, Ashot S Harutyunyan, Bettina Gisslinger, Elisa Rumi, Luca Malcovati, Daniela Pietra, Chiara Elena, Matteo Giovanni Della Porta, Lisa Pieri, Paola Guglielmelli, Christoph Bock, Michael Doubek, Dana Dvorakova, Nada Suvajdzic, Dragica Tomin, Natasa Tosic, Zdenek Racil, Michael Steurer, Sonja Pavlovic, Alessandro M Vannucchi, Mario Cazzola, Heinz Gisslinger, Robert Kralovics
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Publicado: Public Library of Science (PLoS) 2013
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Acceso en línea:https://doaj.org/article/f0ebf7fb82cc41188bd664f89dc8a83f
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spelling oai:doaj.org-article:f0ebf7fb82cc41188bd664f89dc8a83f2021-11-18T08:50:42ZComplex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2.1932-620310.1371/journal.pone.0077819https://doaj.org/article/f0ebf7fb82cc41188bd664f89dc8a83f2013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24147083/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Exome sequencing of primary tumors identifies complex somatic mutation patterns. Assignment of relevance of individual somatic mutations is difficult and poses the next challenge for interpretation of next generation sequencing data. Here we present an approach how exome sequencing in combination with SNP microarray data may identify targets of chromosomal aberrations in myeloid malignancies. The rationale of this approach is that hotspots of chromosomal aberrations might also harbor point mutations in the target genes of deletions, gains or uniparental disomies (UPDs). Chromosome 11 is a frequent target of lesions in myeloid malignancies. Therefore, we studied chromosome 11 in a total of 813 samples from 773 individual patients with different myeloid malignancies by SNP microarrays and complemented the data with exome sequencing in selected cases exhibiting chromosome 11 defects. We found gains, losses and UPDs of chromosome 11 in 52 of the 813 samples (6.4%). Chromosome 11q UPDs frequently associated with mutations of CBL. In one patient the 11qUPD amplified somatic mutations in both CBL and the DNA repair gene DDB1. A duplication within MLL exon 3 was detected in another patient with 11qUPD. We identified several common deleted regions (CDR) on chromosome 11. One of the CDRs associated with de novo acute myeloid leukemia (P=0.013). One patient with a deletion at the LMO2 locus harbored an additional point mutation on the other allele indicating that LMO2 might be a tumor suppressor frequently targeted by 11p deletions. Our chromosome-centered analysis indicates that chromosome 11 contains a number of tumor suppressor genes and that the role of this chromosome in myeloid malignancies is more complex than previously recognized.Thorsten KlampflJelena D MilosevicAna PudaAndreas SchöneggerKlaudia BagienskiTiina BergAshot S HarutyunyanBettina GisslingerElisa RumiLuca MalcovatiDaniela PietraChiara ElenaMatteo Giovanni Della PortaLisa PieriPaola GuglielmelliChristoph BockMichael DoubekDana DvorakovaNada SuvajdzicDragica TominNatasa TosicZdenek RacilMichael SteurerSonja PavlovicAlessandro M VannucchiMario CazzolaHeinz GisslingerRobert KralovicsPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 10, p e77819 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Thorsten Klampfl
Jelena D Milosevic
Ana Puda
Andreas Schönegger
Klaudia Bagienski
Tiina Berg
Ashot S Harutyunyan
Bettina Gisslinger
Elisa Rumi
Luca Malcovati
Daniela Pietra
Chiara Elena
Matteo Giovanni Della Porta
Lisa Pieri
Paola Guglielmelli
Christoph Bock
Michael Doubek
Dana Dvorakova
Nada Suvajdzic
Dragica Tomin
Natasa Tosic
Zdenek Racil
Michael Steurer
Sonja Pavlovic
Alessandro M Vannucchi
Mario Cazzola
Heinz Gisslinger
Robert Kralovics
Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2.
description Exome sequencing of primary tumors identifies complex somatic mutation patterns. Assignment of relevance of individual somatic mutations is difficult and poses the next challenge for interpretation of next generation sequencing data. Here we present an approach how exome sequencing in combination with SNP microarray data may identify targets of chromosomal aberrations in myeloid malignancies. The rationale of this approach is that hotspots of chromosomal aberrations might also harbor point mutations in the target genes of deletions, gains or uniparental disomies (UPDs). Chromosome 11 is a frequent target of lesions in myeloid malignancies. Therefore, we studied chromosome 11 in a total of 813 samples from 773 individual patients with different myeloid malignancies by SNP microarrays and complemented the data with exome sequencing in selected cases exhibiting chromosome 11 defects. We found gains, losses and UPDs of chromosome 11 in 52 of the 813 samples (6.4%). Chromosome 11q UPDs frequently associated with mutations of CBL. In one patient the 11qUPD amplified somatic mutations in both CBL and the DNA repair gene DDB1. A duplication within MLL exon 3 was detected in another patient with 11qUPD. We identified several common deleted regions (CDR) on chromosome 11. One of the CDRs associated with de novo acute myeloid leukemia (P=0.013). One patient with a deletion at the LMO2 locus harbored an additional point mutation on the other allele indicating that LMO2 might be a tumor suppressor frequently targeted by 11p deletions. Our chromosome-centered analysis indicates that chromosome 11 contains a number of tumor suppressor genes and that the role of this chromosome in myeloid malignancies is more complex than previously recognized.
format article
author Thorsten Klampfl
Jelena D Milosevic
Ana Puda
Andreas Schönegger
Klaudia Bagienski
Tiina Berg
Ashot S Harutyunyan
Bettina Gisslinger
Elisa Rumi
Luca Malcovati
Daniela Pietra
Chiara Elena
Matteo Giovanni Della Porta
Lisa Pieri
Paola Guglielmelli
Christoph Bock
Michael Doubek
Dana Dvorakova
Nada Suvajdzic
Dragica Tomin
Natasa Tosic
Zdenek Racil
Michael Steurer
Sonja Pavlovic
Alessandro M Vannucchi
Mario Cazzola
Heinz Gisslinger
Robert Kralovics
author_facet Thorsten Klampfl
Jelena D Milosevic
Ana Puda
Andreas Schönegger
Klaudia Bagienski
Tiina Berg
Ashot S Harutyunyan
Bettina Gisslinger
Elisa Rumi
Luca Malcovati
Daniela Pietra
Chiara Elena
Matteo Giovanni Della Porta
Lisa Pieri
Paola Guglielmelli
Christoph Bock
Michael Doubek
Dana Dvorakova
Nada Suvajdzic
Dragica Tomin
Natasa Tosic
Zdenek Racil
Michael Steurer
Sonja Pavlovic
Alessandro M Vannucchi
Mario Cazzola
Heinz Gisslinger
Robert Kralovics
author_sort Thorsten Klampfl
title Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2.
title_short Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2.
title_full Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2.
title_fullStr Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2.
title_full_unstemmed Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2.
title_sort complex patterns of chromosome 11 aberrations in myeloid malignancies target cbl, mll, ddb1 and lmo2.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/f0ebf7fb82cc41188bd664f89dc8a83f
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