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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/148939
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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 |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1002/1097-0142(20011001)92:7<1992::aid-cncr1719>3.0.co;2-2 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 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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 |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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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13.13397 |