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Scattered genomic amplification in dedifferentiated liposarcoma

BACKGROUND: Atypical lipomatous tumor (ALT), well differentiated liposarcoma (WDLS) and dedifferentiated liposarcoma (DDLS) are cytogenetically characterized by near-diploid karyotypes with no or few other aberrations than supernumerary ring or giant marker chromosomes, although DDLS tend to have so...

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Autores principales: Mandahl, Nils, Magnusson, Linda, Nilsson, Jenny, Viklund, Björn, Arbajian, Elsa, von Steyern, Fredrik Vult, Isaksson, Anders, Mertens, Fredrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5483303/
https://www.ncbi.nlm.nih.gov/pubmed/28652867
http://dx.doi.org/10.1186/s13039-017-0325-5
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author Mandahl, Nils
Magnusson, Linda
Nilsson, Jenny
Viklund, Björn
Arbajian, Elsa
von Steyern, Fredrik Vult
Isaksson, Anders
Mertens, Fredrik
author_facet Mandahl, Nils
Magnusson, Linda
Nilsson, Jenny
Viklund, Björn
Arbajian, Elsa
von Steyern, Fredrik Vult
Isaksson, Anders
Mertens, Fredrik
author_sort Mandahl, Nils
collection PubMed
description BACKGROUND: Atypical lipomatous tumor (ALT), well differentiated liposarcoma (WDLS) and dedifferentiated liposarcoma (DDLS) are cytogenetically characterized by near-diploid karyotypes with no or few other aberrations than supernumerary ring or giant marker chromosomes, although DDLS tend to have somewhat more complex rearrangements. In contrast, pleomorphic liposarcomas (PLS) have highly aberrant and heterogeneous karyotypes. The ring and giant marker chromosomes contain discontinuous amplicons, in particular including multiple copies of the target genes CDK4, HMGA2 and MDM2 from 12q, but often also sequences from other chromosomes. RESULTS: The present study presents a DDLS with an atypical hypertriploid karyotype without any ring or giant marker chromosomes. SNP array analyses revealed amplification of almost the entire 5p and discontinuous amplicons of 12q including the classical target genes, in particular CDK4. In addition, amplicons from 1q, 3q, 7p, 9p, 11q and 20q, covering from 2 to 14 Mb, were present. FISH analyses showed that sequences from 5p and 12q were scattered, separately or together, over more than 10 chromosomes of varying size. At RNA sequencing, significantly elevated expression, compared to myxoid liposarcomas, was seen for TRIO and AMACR in 5p and of CDK4, HMGA2 and MDM2 in 12q. CONCLUSIONS: The observed pattern of scattered amplification does not show the characteristics of chromothripsis, but is novel and differs from the well known cytogenetic manifestations of amplification, i.e., double minutes, homogeneously staining regions and ring chromosomes. Possible explanations for this unusual distribution of amplified sequences might be the mechanism of alternative lengthening of telomeres that is frequently active in DDLS and events associated with telomere crisis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13039-017-0325-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-54833032017-06-26 Scattered genomic amplification in dedifferentiated liposarcoma Mandahl, Nils Magnusson, Linda Nilsson, Jenny Viklund, Björn Arbajian, Elsa von Steyern, Fredrik Vult Isaksson, Anders Mertens, Fredrik Mol Cytogenet Research BACKGROUND: Atypical lipomatous tumor (ALT), well differentiated liposarcoma (WDLS) and dedifferentiated liposarcoma (DDLS) are cytogenetically characterized by near-diploid karyotypes with no or few other aberrations than supernumerary ring or giant marker chromosomes, although DDLS tend to have somewhat more complex rearrangements. In contrast, pleomorphic liposarcomas (PLS) have highly aberrant and heterogeneous karyotypes. The ring and giant marker chromosomes contain discontinuous amplicons, in particular including multiple copies of the target genes CDK4, HMGA2 and MDM2 from 12q, but often also sequences from other chromosomes. RESULTS: The present study presents a DDLS with an atypical hypertriploid karyotype without any ring or giant marker chromosomes. SNP array analyses revealed amplification of almost the entire 5p and discontinuous amplicons of 12q including the classical target genes, in particular CDK4. In addition, amplicons from 1q, 3q, 7p, 9p, 11q and 20q, covering from 2 to 14 Mb, were present. FISH analyses showed that sequences from 5p and 12q were scattered, separately or together, over more than 10 chromosomes of varying size. At RNA sequencing, significantly elevated expression, compared to myxoid liposarcomas, was seen for TRIO and AMACR in 5p and of CDK4, HMGA2 and MDM2 in 12q. CONCLUSIONS: The observed pattern of scattered amplification does not show the characteristics of chromothripsis, but is novel and differs from the well known cytogenetic manifestations of amplification, i.e., double minutes, homogeneously staining regions and ring chromosomes. Possible explanations for this unusual distribution of amplified sequences might be the mechanism of alternative lengthening of telomeres that is frequently active in DDLS and events associated with telomere crisis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13039-017-0325-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-24 /pmc/articles/PMC5483303/ /pubmed/28652867 http://dx.doi.org/10.1186/s13039-017-0325-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Mandahl, Nils
Magnusson, Linda
Nilsson, Jenny
Viklund, Björn
Arbajian, Elsa
von Steyern, Fredrik Vult
Isaksson, Anders
Mertens, Fredrik
Scattered genomic amplification in dedifferentiated liposarcoma
title Scattered genomic amplification in dedifferentiated liposarcoma
title_full Scattered genomic amplification in dedifferentiated liposarcoma
title_fullStr Scattered genomic amplification in dedifferentiated liposarcoma
title_full_unstemmed Scattered genomic amplification in dedifferentiated liposarcoma
title_short Scattered genomic amplification in dedifferentiated liposarcoma
title_sort scattered genomic amplification in dedifferentiated liposarcoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5483303/
https://www.ncbi.nlm.nih.gov/pubmed/28652867
http://dx.doi.org/10.1186/s13039-017-0325-5
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