Karyotype of cryopreserved bone marrow cells

Detalhes bibliográficos
Autor(a) principal: Chauffaille, Maria de Lourdes Lopes Ferrari [UNIFESP]
Data de Publicação: 2003
Outros Autores: Pinheiro, Ronald Feitosa [UNIFESP], Stefano, Jose Tadeu [UNIFESP], Kerbauy, José [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/1775
http://dx.doi.org/10.1590/S0100-879X2003000700004
Resumo: The analysis of chromosomal abnormalities is important for the study of hematological neoplastic disorders since it facilitates classification of the disease. The ability to perform chromosome analysis of cryopreserved malignant marrow or peripheral blast cells is important for retrospective studies. In the present study, we compared the karyotype of fresh bone marrow cells (20 metaphases) to that of cells stored with a simplified cryopreservation method, evaluated the effect of the use of granulocyte-macrophage colony-stimulating factor (GM-CSF) as an in vitro mitotic index stimulator, and compared the cell viability and chromosome morphology of fresh and cryopreserved cells whenever possible (sufficient metaphases for analysis). Twenty-five bone marrow samples from 24 patients with hematological disorders such as acute myeloid leukemia, acute lymphoblastic leukemia, myelodysplastic syndrome, chronic myeloid leukemia, megaloblastic anemia and lymphoma (8, 3, 3, 8, 1, and 1 patients, respectively) were selected at diagnosis, at relapse or during routine follow-up and one sample was obtained from a bone marrow donor after informed consent. Average cell viability before and after freezing was 98.8 and 78.5%, respectively (P < 0.05). Cytogenetic analysis was successful in 76% of fresh cell cultures, as opposed to 52% of cryopreserved samples (P < 0.05). GM-CSF had no proliferative effect before or after freezing. The morphological aspects of the chromosomes in fresh and cryopreserved cells were subjectively the same. The present study shows that cytogenetic analysis of cryopreserved bone marrow cells can be a reliable alternative when fresh cell analysis cannot be done, notwithstanding the reduced viability and lower percent of successful analysis that are associated with freezing.
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spelling Chauffaille, Maria de Lourdes Lopes Ferrari [UNIFESP]Pinheiro, Ronald Feitosa [UNIFESP]Stefano, Jose Tadeu [UNIFESP]Kerbauy, José [UNIFESP]Universidade Federal de São Paulo (UNIFESP)2015-06-14T13:30:04Z2015-06-14T13:30:04Z2003-07-01Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 36, n. 7, p. 845-850, 2003.0100-879Xhttp://repositorio.unifesp.br/handle/11600/1775http://dx.doi.org/10.1590/S0100-879X2003000700004S0100-879X2003000700004.pdfS0100-879X200300070000410.1590/S0100-879X2003000700004WOS:000184240800004The analysis of chromosomal abnormalities is important for the study of hematological neoplastic disorders since it facilitates classification of the disease. The ability to perform chromosome analysis of cryopreserved malignant marrow or peripheral blast cells is important for retrospective studies. In the present study, we compared the karyotype of fresh bone marrow cells (20 metaphases) to that of cells stored with a simplified cryopreservation method, evaluated the effect of the use of granulocyte-macrophage colony-stimulating factor (GM-CSF) as an in vitro mitotic index stimulator, and compared the cell viability and chromosome morphology of fresh and cryopreserved cells whenever possible (sufficient metaphases for analysis). Twenty-five bone marrow samples from 24 patients with hematological disorders such as acute myeloid leukemia, acute lymphoblastic leukemia, myelodysplastic syndrome, chronic myeloid leukemia, megaloblastic anemia and lymphoma (8, 3, 3, 8, 1, and 1 patients, respectively) were selected at diagnosis, at relapse or during routine follow-up and one sample was obtained from a bone marrow donor after informed consent. Average cell viability before and after freezing was 98.8 and 78.5%, respectively (P < 0.05). Cytogenetic analysis was successful in 76% of fresh cell cultures, as opposed to 52% of cryopreserved samples (P < 0.05). GM-CSF had no proliferative effect before or after freezing. The morphological aspects of the chromosomes in fresh and cryopreserved cells were subjectively the same. The present study shows that cytogenetic analysis of cryopreserved bone marrow cells can be a reliable alternative when fresh cell analysis cannot be done, notwithstanding the reduced viability and lower percent of successful analysis that are associated with freezing.Universidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Disciplina de Hematologia e HemoterapiaUNIFESP, EPM, Disciplina de Hematologia e HemoterapiaSciELO845-850engAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological ResearchCryopreservationKaryotypeBone marrow cellsKaryotype of cryopreserved bone marrow cellsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALS0100-879X2003000700004.pdfapplication/pdf483041${dspace.ui.url}/bitstream/11600/1775/1/S0100-879X2003000700004.pdf7749685da03f8f96a24154b2e1ee57bfMD51open accessTEXTS0100-879X2003000700004.pdf.txtS0100-879X2003000700004.pdf.txtExtracted texttext/plain21321${dspace.ui.url}/bitstream/11600/1775/2/S0100-879X2003000700004.pdf.txtcee8f58754ac214e5d0c051de3094ba3MD52open access11600/17752022-06-02 09:02:19.233open accessoai:repositorio.unifesp.br:11600/1775Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-05-25T12:13:38.696975Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Karyotype of cryopreserved bone marrow cells
title Karyotype of cryopreserved bone marrow cells
spellingShingle Karyotype of cryopreserved bone marrow cells
Chauffaille, Maria de Lourdes Lopes Ferrari [UNIFESP]
Cryopreservation
Karyotype
Bone marrow cells
title_short Karyotype of cryopreserved bone marrow cells
title_full Karyotype of cryopreserved bone marrow cells
title_fullStr Karyotype of cryopreserved bone marrow cells
title_full_unstemmed Karyotype of cryopreserved bone marrow cells
title_sort Karyotype of cryopreserved bone marrow cells
author Chauffaille, Maria de Lourdes Lopes Ferrari [UNIFESP]
author_facet Chauffaille, Maria de Lourdes Lopes Ferrari [UNIFESP]
Pinheiro, Ronald Feitosa [UNIFESP]
Stefano, Jose Tadeu [UNIFESP]
Kerbauy, José [UNIFESP]
author_role author
author2 Pinheiro, Ronald Feitosa [UNIFESP]
Stefano, Jose Tadeu [UNIFESP]
Kerbauy, José [UNIFESP]
author2_role author
author
author
dc.contributor.institution.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Chauffaille, Maria de Lourdes Lopes Ferrari [UNIFESP]
Pinheiro, Ronald Feitosa [UNIFESP]
Stefano, Jose Tadeu [UNIFESP]
Kerbauy, José [UNIFESP]
dc.subject.eng.fl_str_mv Cryopreservation
Karyotype
Bone marrow cells
topic Cryopreservation
Karyotype
Bone marrow cells
description The analysis of chromosomal abnormalities is important for the study of hematological neoplastic disorders since it facilitates classification of the disease. The ability to perform chromosome analysis of cryopreserved malignant marrow or peripheral blast cells is important for retrospective studies. In the present study, we compared the karyotype of fresh bone marrow cells (20 metaphases) to that of cells stored with a simplified cryopreservation method, evaluated the effect of the use of granulocyte-macrophage colony-stimulating factor (GM-CSF) as an in vitro mitotic index stimulator, and compared the cell viability and chromosome morphology of fresh and cryopreserved cells whenever possible (sufficient metaphases for analysis). Twenty-five bone marrow samples from 24 patients with hematological disorders such as acute myeloid leukemia, acute lymphoblastic leukemia, myelodysplastic syndrome, chronic myeloid leukemia, megaloblastic anemia and lymphoma (8, 3, 3, 8, 1, and 1 patients, respectively) were selected at diagnosis, at relapse or during routine follow-up and one sample was obtained from a bone marrow donor after informed consent. Average cell viability before and after freezing was 98.8 and 78.5%, respectively (P < 0.05). Cytogenetic analysis was successful in 76% of fresh cell cultures, as opposed to 52% of cryopreserved samples (P < 0.05). GM-CSF had no proliferative effect before or after freezing. The morphological aspects of the chromosomes in fresh and cryopreserved cells were subjectively the same. The present study shows that cytogenetic analysis of cryopreserved bone marrow cells can be a reliable alternative when fresh cell analysis cannot be done, notwithstanding the reduced viability and lower percent of successful analysis that are associated with freezing.
publishDate 2003
dc.date.issued.fl_str_mv 2003-07-01
dc.date.accessioned.fl_str_mv 2015-06-14T13:30:04Z
dc.date.available.fl_str_mv 2015-06-14T13:30:04Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.citation.fl_str_mv Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 36, n. 7, p. 845-850, 2003.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/1775
http://dx.doi.org/10.1590/S0100-879X2003000700004
dc.identifier.issn.none.fl_str_mv 0100-879X
dc.identifier.file.none.fl_str_mv S0100-879X2003000700004.pdf
dc.identifier.scielo.none.fl_str_mv S0100-879X2003000700004
dc.identifier.doi.none.fl_str_mv 10.1590/S0100-879X2003000700004
dc.identifier.wos.none.fl_str_mv WOS:000184240800004
identifier_str_mv Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 36, n. 7, p. 845-850, 2003.
0100-879X
S0100-879X2003000700004.pdf
S0100-879X2003000700004
10.1590/S0100-879X2003000700004
WOS:000184240800004
url http://repositorio.unifesp.br/handle/11600/1775
http://dx.doi.org/10.1590/S0100-879X2003000700004
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Brazilian Journal of Medical and Biological Research
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dc.format.none.fl_str_mv 845-850
dc.publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
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