A comparative genomic hybridization study on postirradiation sarcomas

Autores
Tarkkanen, Maija; Wiklund, Tom A.; Virolainen, Martti J.; Larramendy, Marcelo Luis; Mandahl, Nils; Mertens, Fredrik; Blomqvist, Carl P.; Tukiainen, Erkki J.; Miettinen, Markku M. A.; Elomaa, A. Inkeri; Knuutila, Y. Sakari
Año de publicación
2001
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Background: Radiotherapy is a known risk factor for sarcoma development. Postirradiation sarcomas arise within the radiation field after a latency period of several years and usually are highly malignant. Very little is yet known about their genetic changes. Methods: Twenty-seven postirradiation sarcomas were analyzed by comparative genomic hybridization, which allows genome-wide screening of DNA sequence copy number changes. Results: Copy-number aberrations were detected in 20 (74%) tumors. The mean number of aberrations per tumor was 5.3 with gains outnumbering losses. The most frequent gains affected the minimal common regions of 7q11.2-q21 and 7q22 in 30% and 7p15-pter in 26%. Gain of 8q23-qter was detected in 22%. The most frequent losses affected 11q23-qter and 13q22-q32 in 22%. In osteosarcomas, the most frequent aberration was loss of 1p21-p31, in malignant fibrous histiocytomas (MFH) gain of 7cen-q22, and in fibrosarcomas gain of 7q22. The findings in postirradiation osteosarcomas and MFHs were compared with findings in sporadic osteosarcomas and MFHs, reported previously by the authors. In sporadic osteosarcomas, gains outnumbered losses, but, in postirradiation osteosarcomas, losses were more frequent than gains. Loss at 1p was rare in sporadic osteosarcoma (3%) but frequent (57%) in postirradiation osteosarcomas. Gains at 7q were frequent both in postirradiation and sporadic MFH. Conclusions: According to previous studies on different types of sporadic sarcomas, gains at 7q or 8q are associated with poor prognosis or large tumor size. Thus, the frequent gains at 7q and 8q might have been responsible in part for the poor prognosis of postirradiation sarcomas. Also, however, some of their clinical features, i.e., high malignancy grade, late diagnosis, and central location, are associated with a poor prognosis.
Fil: Tarkkanen, Maija. University of Helsinki; Finlandia. Helsinki University Central Hospital; Finlandia
Fil: Wiklund, Tom A.. Helsinki University Central Hospital; Finlandia
Fil: Virolainen, Martti J.. University of Helsinki; Finlandia
Fil: Larramendy, Marcelo Luis. Universidad Nacional de La Plata. Facultad de Ciencias Naturales y Museo. Laboratorio de Citogenética; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata; Argentina. Helsinki University Central Hospital; Finlandia. University of Helsinki; Finlandia
Fil: Mandahl, Nils. Lund University; Suecia
Fil: Mertens, Fredrik. Lund University; Suecia
Fil: Blomqvist, Carl P.. Helsinki University Central Hospital; Finlandia
Fil: Tukiainen, Erkki J.. Helsinki University Central Hospital; Finlandia
Fil: Miettinen, Markku M. A.. University of Helsinki; Finlandia
Fil: Elomaa, A. Inkeri. Helsinki University Central Hospital; Finlandia
Fil: Knuutila, Y. Sakari. University of Helsinki; Finlandia
Materia
Postirradiation sarcomas
Comparative genomic hybridization
Angiosarcoma
Osteosarcoma
Fibrosarcoma
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/148939

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network_name_str CONICET Digital (CONICET)
spelling A comparative genomic hybridization study on postirradiation sarcomasTarkkanen, MaijaWiklund, Tom A.Virolainen, Martti J.Larramendy, Marcelo LuisMandahl, NilsMertens, FredrikBlomqvist, Carl P.Tukiainen, Erkki J.Miettinen, Markku M. A.Elomaa, A. InkeriKnuutila, Y. SakariPostirradiation sarcomasComparative genomic hybridizationAngiosarcomaOsteosarcomaFibrosarcomahttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Background: Radiotherapy is a known risk factor for sarcoma development. Postirradiation sarcomas arise within the radiation field after a latency period of several years and usually are highly malignant. Very little is yet known about their genetic changes. Methods: Twenty-seven postirradiation sarcomas were analyzed by comparative genomic hybridization, which allows genome-wide screening of DNA sequence copy number changes. Results: Copy-number aberrations were detected in 20 (74%) tumors. The mean number of aberrations per tumor was 5.3 with gains outnumbering losses. The most frequent gains affected the minimal common regions of 7q11.2-q21 and 7q22 in 30% and 7p15-pter in 26%. Gain of 8q23-qter was detected in 22%. The most frequent losses affected 11q23-qter and 13q22-q32 in 22%. In osteosarcomas, the most frequent aberration was loss of 1p21-p31, in malignant fibrous histiocytomas (MFH) gain of 7cen-q22, and in fibrosarcomas gain of 7q22. The findings in postirradiation osteosarcomas and MFHs were compared with findings in sporadic osteosarcomas and MFHs, reported previously by the authors. In sporadic osteosarcomas, gains outnumbered losses, but, in postirradiation osteosarcomas, losses were more frequent than gains. Loss at 1p was rare in sporadic osteosarcoma (3%) but frequent (57%) in postirradiation osteosarcomas. Gains at 7q were frequent both in postirradiation and sporadic MFH. Conclusions: According to previous studies on different types of sporadic sarcomas, gains at 7q or 8q are associated with poor prognosis or large tumor size. Thus, the frequent gains at 7q and 8q might have been responsible in part for the poor prognosis of postirradiation sarcomas. Also, however, some of their clinical features, i.e., high malignancy grade, late diagnosis, and central location, are associated with a poor prognosis.Fil: Tarkkanen, Maija. University of Helsinki; Finlandia. Helsinki University Central Hospital; FinlandiaFil: Wiklund, Tom A.. Helsinki University Central Hospital; FinlandiaFil: Virolainen, Martti J.. University of Helsinki; FinlandiaFil: Larramendy, Marcelo Luis. Universidad Nacional de La Plata. Facultad de Ciencias Naturales y Museo. Laboratorio de Citogenética; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata; Argentina. Helsinki University Central Hospital; Finlandia. University of Helsinki; FinlandiaFil: Mandahl, Nils. Lund University; SueciaFil: Mertens, Fredrik. Lund University; SueciaFil: Blomqvist, Carl P.. Helsinki University Central Hospital; FinlandiaFil: Tukiainen, Erkki J.. Helsinki University Central Hospital; FinlandiaFil: Miettinen, Markku M. A.. University of Helsinki; FinlandiaFil: Elomaa, A. Inkeri. Helsinki University Central Hospital; FinlandiaFil: Knuutila, Y. Sakari. University of Helsinki; FinlandiaJohn Wiley & Sons Inc2001-10-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/148939Tarkkanen, Maija; Wiklund, Tom A.; Virolainen, Martti J.; Larramendy, Marcelo Luis; Mandahl, Nils; et al.; A comparative genomic hybridization study on postirradiation sarcomas; John Wiley & Sons Inc; Cancer; 92; 7; 8-10-2001; 1992-19980008-543XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1002/1097-0142(20011001)92:7<1992::aid-cncr1719>3.0.co;2-2info:eu-repo/semantics/altIdentifier/url/https://acsjournals.onlinelibrary.wiley.com/doi/10.1002/1097-0142(20011001)92:7%3C1992::AID-CNCR1719%3E3.0.CO;2-2info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:59:57Zoai:ri.conicet.gov.ar:11336/148939instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:59:57.765CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv A comparative genomic hybridization study on postirradiation sarcomas
title A comparative genomic hybridization study on postirradiation sarcomas
spellingShingle A comparative genomic hybridization study on postirradiation sarcomas
Tarkkanen, Maija
Postirradiation sarcomas
Comparative genomic hybridization
Angiosarcoma
Osteosarcoma
Fibrosarcoma
title_short A comparative genomic hybridization study on postirradiation sarcomas
title_full A comparative genomic hybridization study on postirradiation sarcomas
title_fullStr A comparative genomic hybridization study on postirradiation sarcomas
title_full_unstemmed A comparative genomic hybridization study on postirradiation sarcomas
title_sort A comparative genomic hybridization study on postirradiation sarcomas
dc.creator.none.fl_str_mv Tarkkanen, Maija
Wiklund, Tom A.
Virolainen, Martti J.
Larramendy, Marcelo Luis
Mandahl, Nils
Mertens, Fredrik
Blomqvist, Carl P.
Tukiainen, Erkki J.
Miettinen, Markku M. A.
Elomaa, A. Inkeri
Knuutila, Y. Sakari
author Tarkkanen, Maija
author_facet Tarkkanen, Maija
Wiklund, Tom A.
Virolainen, Martti J.
Larramendy, Marcelo Luis
Mandahl, Nils
Mertens, Fredrik
Blomqvist, Carl P.
Tukiainen, Erkki J.
Miettinen, Markku M. A.
Elomaa, A. Inkeri
Knuutila, Y. Sakari
author_role author
author2 Wiklund, Tom A.
Virolainen, Martti J.
Larramendy, Marcelo Luis
Mandahl, Nils
Mertens, Fredrik
Blomqvist, Carl P.
Tukiainen, Erkki J.
Miettinen, Markku M. A.
Elomaa, A. Inkeri
Knuutila, Y. Sakari
author2_role author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Postirradiation sarcomas
Comparative genomic hybridization
Angiosarcoma
Osteosarcoma
Fibrosarcoma
topic Postirradiation sarcomas
Comparative genomic hybridization
Angiosarcoma
Osteosarcoma
Fibrosarcoma
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Background: Radiotherapy is a known risk factor for sarcoma development. Postirradiation sarcomas arise within the radiation field after a latency period of several years and usually are highly malignant. Very little is yet known about their genetic changes. Methods: Twenty-seven postirradiation sarcomas were analyzed by comparative genomic hybridization, which allows genome-wide screening of DNA sequence copy number changes. Results: Copy-number aberrations were detected in 20 (74%) tumors. The mean number of aberrations per tumor was 5.3 with gains outnumbering losses. The most frequent gains affected the minimal common regions of 7q11.2-q21 and 7q22 in 30% and 7p15-pter in 26%. Gain of 8q23-qter was detected in 22%. The most frequent losses affected 11q23-qter and 13q22-q32 in 22%. In osteosarcomas, the most frequent aberration was loss of 1p21-p31, in malignant fibrous histiocytomas (MFH) gain of 7cen-q22, and in fibrosarcomas gain of 7q22. The findings in postirradiation osteosarcomas and MFHs were compared with findings in sporadic osteosarcomas and MFHs, reported previously by the authors. In sporadic osteosarcomas, gains outnumbered losses, but, in postirradiation osteosarcomas, losses were more frequent than gains. Loss at 1p was rare in sporadic osteosarcoma (3%) but frequent (57%) in postirradiation osteosarcomas. Gains at 7q were frequent both in postirradiation and sporadic MFH. Conclusions: According to previous studies on different types of sporadic sarcomas, gains at 7q or 8q are associated with poor prognosis or large tumor size. Thus, the frequent gains at 7q and 8q might have been responsible in part for the poor prognosis of postirradiation sarcomas. Also, however, some of their clinical features, i.e., high malignancy grade, late diagnosis, and central location, are associated with a poor prognosis.
Fil: Tarkkanen, Maija. University of Helsinki; Finlandia. Helsinki University Central Hospital; Finlandia
Fil: Wiklund, Tom A.. Helsinki University Central Hospital; Finlandia
Fil: Virolainen, Martti J.. University of Helsinki; Finlandia
Fil: Larramendy, Marcelo Luis. Universidad Nacional de La Plata. Facultad de Ciencias Naturales y Museo. Laboratorio de Citogenética; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata; Argentina. Helsinki University Central Hospital; Finlandia. University of Helsinki; Finlandia
Fil: Mandahl, Nils. Lund University; Suecia
Fil: Mertens, Fredrik. Lund University; Suecia
Fil: Blomqvist, Carl P.. Helsinki University Central Hospital; Finlandia
Fil: Tukiainen, Erkki J.. Helsinki University Central Hospital; Finlandia
Fil: Miettinen, Markku M. A.. University of Helsinki; Finlandia
Fil: Elomaa, A. Inkeri. Helsinki University Central Hospital; Finlandia
Fil: Knuutila, Y. Sakari. University of Helsinki; Finlandia
description Background: Radiotherapy is a known risk factor for sarcoma development. Postirradiation sarcomas arise within the radiation field after a latency period of several years and usually are highly malignant. Very little is yet known about their genetic changes. Methods: Twenty-seven postirradiation sarcomas were analyzed by comparative genomic hybridization, which allows genome-wide screening of DNA sequence copy number changes. Results: Copy-number aberrations were detected in 20 (74%) tumors. The mean number of aberrations per tumor was 5.3 with gains outnumbering losses. The most frequent gains affected the minimal common regions of 7q11.2-q21 and 7q22 in 30% and 7p15-pter in 26%. Gain of 8q23-qter was detected in 22%. The most frequent losses affected 11q23-qter and 13q22-q32 in 22%. In osteosarcomas, the most frequent aberration was loss of 1p21-p31, in malignant fibrous histiocytomas (MFH) gain of 7cen-q22, and in fibrosarcomas gain of 7q22. The findings in postirradiation osteosarcomas and MFHs were compared with findings in sporadic osteosarcomas and MFHs, reported previously by the authors. In sporadic osteosarcomas, gains outnumbered losses, but, in postirradiation osteosarcomas, losses were more frequent than gains. Loss at 1p was rare in sporadic osteosarcoma (3%) but frequent (57%) in postirradiation osteosarcomas. Gains at 7q were frequent both in postirradiation and sporadic MFH. Conclusions: According to previous studies on different types of sporadic sarcomas, gains at 7q or 8q are associated with poor prognosis or large tumor size. Thus, the frequent gains at 7q and 8q might have been responsible in part for the poor prognosis of postirradiation sarcomas. Also, however, some of their clinical features, i.e., high malignancy grade, late diagnosis, and central location, are associated with a poor prognosis.
publishDate 2001
dc.date.none.fl_str_mv 2001-10-08
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/148939
Tarkkanen, Maija; Wiklund, Tom A.; Virolainen, Martti J.; Larramendy, Marcelo Luis; Mandahl, Nils; et al.; A comparative genomic hybridization study on postirradiation sarcomas; John Wiley & Sons Inc; Cancer; 92; 7; 8-10-2001; 1992-1998
0008-543X
CONICET Digital
CONICET
url http://hdl.handle.net/11336/148939
identifier_str_mv Tarkkanen, Maija; Wiklund, Tom A.; Virolainen, Martti J.; Larramendy, Marcelo Luis; Mandahl, Nils; et al.; A comparative genomic hybridization study on postirradiation sarcomas; John Wiley & Sons Inc; Cancer; 92; 7; 8-10-2001; 1992-1998
0008-543X
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
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info:eu-repo/semantics/altIdentifier/url/https://acsjournals.onlinelibrary.wiley.com/doi/10.1002/1097-0142(20011001)92:7%3C1992::AID-CNCR1719%3E3.0.CO;2-2
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dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv John Wiley & Sons Inc
publisher.none.fl_str_mv John Wiley & Sons Inc
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repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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