author_facet Javanmardi, Niloufar
Fransson, Susanne
Djos, Anna
Umapathy, Ganesh
Östensson, Malin
Milosevic, Jelena
Borenäs, Marcus
Hallberg, Bengt
Kogner, Per
Martinsson, Tommy
Palmer, Ruth H.
Javanmardi, Niloufar
Fransson, Susanne
Djos, Anna
Umapathy, Ganesh
Östensson, Malin
Milosevic, Jelena
Borenäs, Marcus
Hallberg, Bengt
Kogner, Per
Martinsson, Tommy
Palmer, Ruth H.
author Javanmardi, Niloufar
Fransson, Susanne
Djos, Anna
Umapathy, Ganesh
Östensson, Malin
Milosevic, Jelena
Borenäs, Marcus
Hallberg, Bengt
Kogner, Per
Martinsson, Tommy
Palmer, Ruth H.
spellingShingle Javanmardi, Niloufar
Fransson, Susanne
Djos, Anna
Umapathy, Ganesh
Östensson, Malin
Milosevic, Jelena
Borenäs, Marcus
Hallberg, Bengt
Kogner, Per
Martinsson, Tommy
Palmer, Ruth H.
Genes, Chromosomes and Cancer
Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements
Cancer Research
Genetics
author_sort javanmardi, niloufar
spelling Javanmardi, Niloufar Fransson, Susanne Djos, Anna Umapathy, Ganesh Östensson, Malin Milosevic, Jelena Borenäs, Marcus Hallberg, Bengt Kogner, Per Martinsson, Tommy Palmer, Ruth H. 1045-2257 1098-2264 Wiley Cancer Research Genetics http://dx.doi.org/10.1002/gcc.22790 <jats:title>Abstract</jats:title><jats:p>Gain of chromosome arm 2p is a previously described entity in neuroblastoma (NB). This genomic address is home to two important oncogenes in NB—<jats:italic>MYCN</jats:italic> and anaplastic lymphoma kinase (<jats:italic>ALK</jats:italic>). <jats:italic>MYCN</jats:italic> amplification is a critical prognostic factor coupled with poor prognosis in NB. Mutation of the ALK receptor tyrosine kinase has been described in both somatic and familial NB. Here, ALK activation occurs in the context of the full‐length receptor, exemplified by activating point mutations in NB. ALK overexpression and activation, in the absence of genetic mutation has also been described in NB. In addition, the recently identified ALK ligand ALKAL2 (previously described as FAM150B and AUGα) is also found on the distal portion of 2p, at 2p25. Here we analyze 356 NB tumor samples and discuss observations indicating that gain of 2p has implications for the development of NB. Finally, we put forward the hypothesis that the effect of 2p gain may result from a combination of <jats:italic>MYCN</jats:italic>, <jats:italic>ALK</jats:italic>, and the ALK ligand <jats:italic>ALKAL2</jats:italic>.</jats:p> Analysis of <i>ALK</i>, <i>MYCN</i>, and the ALK ligand <i>ALKAL2</i> (<i>FAM150B/AUGα</i>) in neuroblastoma patient samples with chromosome arm 2p rearrangements Genes, Chromosomes and Cancer
doi_str_mv 10.1002/gcc.22790
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series Genes, Chromosomes and Cancer
source_id 49
title Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements
title_unstemmed Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements
title_full Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements
title_fullStr Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements
title_full_unstemmed Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements
title_short Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements
title_sort analysis of <i>alk</i>, <i>mycn</i>, and the alk ligand <i>alkal2</i> (<i>fam150b/augα</i>) in neuroblastoma patient samples with chromosome arm 2p rearrangements
topic Cancer Research
Genetics
url http://dx.doi.org/10.1002/gcc.22790
publishDate 2020
physical 50-57
description <jats:title>Abstract</jats:title><jats:p>Gain of chromosome arm 2p is a previously described entity in neuroblastoma (NB). This genomic address is home to two important oncogenes in NB—<jats:italic>MYCN</jats:italic> and anaplastic lymphoma kinase (<jats:italic>ALK</jats:italic>). <jats:italic>MYCN</jats:italic> amplification is a critical prognostic factor coupled with poor prognosis in NB. Mutation of the ALK receptor tyrosine kinase has been described in both somatic and familial NB. Here, ALK activation occurs in the context of the full‐length receptor, exemplified by activating point mutations in NB. ALK overexpression and activation, in the absence of genetic mutation has also been described in NB. In addition, the recently identified ALK ligand ALKAL2 (previously described as FAM150B and AUGα) is also found on the distal portion of 2p, at 2p25. Here we analyze 356 NB tumor samples and discuss observations indicating that gain of 2p has implications for the development of NB. Finally, we put forward the hypothesis that the effect of 2p gain may result from a combination of <jats:italic>MYCN</jats:italic>, <jats:italic>ALK</jats:italic>, and the ALK ligand <jats:italic>ALKAL2</jats:italic>.</jats:p>
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author Javanmardi, Niloufar, Fransson, Susanne, Djos, Anna, Umapathy, Ganesh, Östensson, Malin, Milosevic, Jelena, Borenäs, Marcus, Hallberg, Bengt, Kogner, Per, Martinsson, Tommy, Palmer, Ruth H.
author_facet Javanmardi, Niloufar, Fransson, Susanne, Djos, Anna, Umapathy, Ganesh, Östensson, Malin, Milosevic, Jelena, Borenäs, Marcus, Hallberg, Bengt, Kogner, Per, Martinsson, Tommy, Palmer, Ruth H., Javanmardi, Niloufar, Fransson, Susanne, Djos, Anna, Umapathy, Ganesh, Östensson, Malin, Milosevic, Jelena, Borenäs, Marcus, Hallberg, Bengt, Kogner, Per, Martinsson, Tommy, Palmer, Ruth H.
author_sort javanmardi, niloufar
container_issue 1
container_start_page 50
container_title Genes, Chromosomes and Cancer
container_volume 59
description <jats:title>Abstract</jats:title><jats:p>Gain of chromosome arm 2p is a previously described entity in neuroblastoma (NB). This genomic address is home to two important oncogenes in NB—<jats:italic>MYCN</jats:italic> and anaplastic lymphoma kinase (<jats:italic>ALK</jats:italic>). <jats:italic>MYCN</jats:italic> amplification is a critical prognostic factor coupled with poor prognosis in NB. Mutation of the ALK receptor tyrosine kinase has been described in both somatic and familial NB. Here, ALK activation occurs in the context of the full‐length receptor, exemplified by activating point mutations in NB. ALK overexpression and activation, in the absence of genetic mutation has also been described in NB. In addition, the recently identified ALK ligand ALKAL2 (previously described as FAM150B and AUGα) is also found on the distal portion of 2p, at 2p25. Here we analyze 356 NB tumor samples and discuss observations indicating that gain of 2p has implications for the development of NB. Finally, we put forward the hypothesis that the effect of 2p gain may result from a combination of <jats:italic>MYCN</jats:italic>, <jats:italic>ALK</jats:italic>, and the ALK ligand <jats:italic>ALKAL2</jats:italic>.</jats:p>
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spelling Javanmardi, Niloufar Fransson, Susanne Djos, Anna Umapathy, Ganesh Östensson, Malin Milosevic, Jelena Borenäs, Marcus Hallberg, Bengt Kogner, Per Martinsson, Tommy Palmer, Ruth H. 1045-2257 1098-2264 Wiley Cancer Research Genetics http://dx.doi.org/10.1002/gcc.22790 <jats:title>Abstract</jats:title><jats:p>Gain of chromosome arm 2p is a previously described entity in neuroblastoma (NB). This genomic address is home to two important oncogenes in NB—<jats:italic>MYCN</jats:italic> and anaplastic lymphoma kinase (<jats:italic>ALK</jats:italic>). <jats:italic>MYCN</jats:italic> amplification is a critical prognostic factor coupled with poor prognosis in NB. Mutation of the ALK receptor tyrosine kinase has been described in both somatic and familial NB. Here, ALK activation occurs in the context of the full‐length receptor, exemplified by activating point mutations in NB. ALK overexpression and activation, in the absence of genetic mutation has also been described in NB. In addition, the recently identified ALK ligand ALKAL2 (previously described as FAM150B and AUGα) is also found on the distal portion of 2p, at 2p25. Here we analyze 356 NB tumor samples and discuss observations indicating that gain of 2p has implications for the development of NB. Finally, we put forward the hypothesis that the effect of 2p gain may result from a combination of <jats:italic>MYCN</jats:italic>, <jats:italic>ALK</jats:italic>, and the ALK ligand <jats:italic>ALKAL2</jats:italic>.</jats:p> Analysis of <i>ALK</i>, <i>MYCN</i>, and the ALK ligand <i>ALKAL2</i> (<i>FAM150B/AUGα</i>) in neuroblastoma patient samples with chromosome arm 2p rearrangements Genes, Chromosomes and Cancer
spellingShingle Javanmardi, Niloufar, Fransson, Susanne, Djos, Anna, Umapathy, Ganesh, Östensson, Malin, Milosevic, Jelena, Borenäs, Marcus, Hallberg, Bengt, Kogner, Per, Martinsson, Tommy, Palmer, Ruth H., Genes, Chromosomes and Cancer, Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements, Cancer Research, Genetics
title Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements
title_full Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements
title_fullStr Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements
title_full_unstemmed Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements
title_short Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements
title_sort analysis of <i>alk</i>, <i>mycn</i>, and the alk ligand <i>alkal2</i> (<i>fam150b/augα</i>) in neuroblastoma patient samples with chromosome arm 2p rearrangements
title_unstemmed Analysis of ALK, MYCN, and the ALK ligand ALKAL2 (FAM150B/AUGα) in neuroblastoma patient samples with chromosome arm 2p rearrangements
topic Cancer Research, Genetics
url http://dx.doi.org/10.1002/gcc.22790