Correlation between the cellular expression of CD44 and the forms of acute lymphoblastic leukemia
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Revista Brasileira de Cancerologia (Online) |
Texto Completo: | https://rbc.inca.gov.br/index.php/revista/article/view/2834 |
Resumo: | CD44 is an adhesion molecule expressed by B and T lymphocytes, that mediates cell attachment to extraceliular matrix componentes and adhesion to endothelial cells. The purpose of this study is to investigate the CD44 expression in 108 patients with lymphoblastic leukemia (57 B lineage ALL and 51 T-cell ALL) with a methodology that includes morphological analysis and immunophenotyping with a panel of monoclonal antibodies detected by standard techniques such as immunoperoxidase conjugated methods and flow-cytometry. lnitially we investigated the correlation of CD44 expression with all levels of cellular maturation of these leukemia, established according to antigen expression. Then, we investigated the correlation of this molecule with clinical-pathologic features such as mediastinal mass, adenomegaly and infiltration of the central nervous systein, and number of blastic cells in peripheral blood. In addition, we also investigated CD44 expression in peripheral lymphocytesfrom 11 healthy individuais. The CD44 expression was positive in 83 (76.8%) out of 108 ALL cases studied. In B precursors and B-ALL its expression was observed in 46 (80.8%) out of 57 cases and 37(72.5%) out of 51 cases of T-ALL. In the four subgroups of B precursor ALL, the expression of this molecule was found in 2 cases (66.7%) of null-ALL, in 34 cases (73.5%) of C-ALL and al cases of pre-B (cµ+) and B-ALL (Smlg+). Considering, T-cell ALL, the CD44 expression was variable among the three subgroups of this leukemia. In Subgroup 1 (pre-TALL) all 9 cases were positive (100%). In 14 Subgroups 11 (intermediate T-cell ALL) CD44 was positive in 4 cases (28.6%) and amongst the 28 cases of Subgroup III, CD44 was positive in 24 cases (85.7%). In lymphocytes from the control groups, CD44 expression was positive in all cases with percentages of reactivity ranging from 80% to 100% of cases, which homogeneously exhibited high density of CD44, as assessed by cytofluorimetrv. The correlation of CD44 expression in terms of clinical-pathologic profile o fALL demonstrated that high levels of CD44 were associated to tumoral forms of disease expressed as lymphadenopathy, hepatomegaly, splenomegaly, tumoral masses and infiltration of central nervous system. However, we did not find any association between CD44 and high leveis of circulating blast cells. These data suggest that CD44 should be considered au addicional marker to monitor evolution and asses the mechanisms of pathological evolution of the lvmphohlastic leukemia. |
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Correlation between the cellular expression of CD44 and the forms of acute lymphoblastic leukemiaCorrelação entre a expressão celular do CD44 e formas tumorais das leucemias linfoblásticasAnticorpo Monoclonal CD44Leucemia Linfóide AgudaCD44 Monoclonal AntibodyAcute Lymphoid LeukemiaCD44 is an adhesion molecule expressed by B and T lymphocytes, that mediates cell attachment to extraceliular matrix componentes and adhesion to endothelial cells. The purpose of this study is to investigate the CD44 expression in 108 patients with lymphoblastic leukemia (57 B lineage ALL and 51 T-cell ALL) with a methodology that includes morphological analysis and immunophenotyping with a panel of monoclonal antibodies detected by standard techniques such as immunoperoxidase conjugated methods and flow-cytometry. lnitially we investigated the correlation of CD44 expression with all levels of cellular maturation of these leukemia, established according to antigen expression. Then, we investigated the correlation of this molecule with clinical-pathologic features such as mediastinal mass, adenomegaly and infiltration of the central nervous systein, and number of blastic cells in peripheral blood. In addition, we also investigated CD44 expression in peripheral lymphocytesfrom 11 healthy individuais. The CD44 expression was positive in 83 (76.8%) out of 108 ALL cases studied. In B precursors and B-ALL its expression was observed in 46 (80.8%) out of 57 cases and 37(72.5%) out of 51 cases of T-ALL. In the four subgroups of B precursor ALL, the expression of this molecule was found in 2 cases (66.7%) of null-ALL, in 34 cases (73.5%) of C-ALL and al cases of pre-B (cµ+) and B-ALL (Smlg+). Considering, T-cell ALL, the CD44 expression was variable among the three subgroups of this leukemia. In Subgroup 1 (pre-TALL) all 9 cases were positive (100%). In 14 Subgroups 11 (intermediate T-cell ALL) CD44 was positive in 4 cases (28.6%) and amongst the 28 cases of Subgroup III, CD44 was positive in 24 cases (85.7%). In lymphocytes from the control groups, CD44 expression was positive in all cases with percentages of reactivity ranging from 80% to 100% of cases, which homogeneously exhibited high density of CD44, as assessed by cytofluorimetrv. The correlation of CD44 expression in terms of clinical-pathologic profile o fALL demonstrated that high levels of CD44 were associated to tumoral forms of disease expressed as lymphadenopathy, hepatomegaly, splenomegaly, tumoral masses and infiltration of central nervous system. However, we did not find any association between CD44 and high leveis of circulating blast cells. These data suggest that CD44 should be considered au addicional marker to monitor evolution and asses the mechanisms of pathological evolution of the lvmphohlastic leukemia.O CD44 é uma molécula de adesão que se expressa em linfócitos-B e T, participa na mediação de adesão destas células e dos componentes da matriz extracelular e na adesão a células endoteliais vasculares. A proposta desde estudo foi a de investigar a expressão celular do CD44 em 108 pacientes portadores de leucemias linfoblásticas (57 leucemias linfóides agudas de linhagem B e 51 de células-T), através de uma metodologia que inclui a análise citomorfológica e imunofenotipagem, com um painel de anticorpos monoclonais detectados pelas técnicas da imunoperoxidase conjugada, e imunofluorescência com análise por citometria de fluxo. Inicialmente, investigamos a correlação do CD44 com as distintas fases de diferenciação celular destas leucemias determinadas pela expressão antigênica Em seguida investigamos a correlação desta molécula com os achados clinico-patologicos como a presença de massas tumorais adenomegalias, infiltração de células leucêmicas no sistema nervoso central e em outros órgãos, além da presença de células blásticas no sangue periférico. Paralelamente ao estudo das leucemias, também investigamos a expressão de CD44 em linfócitos do sangue periférico oriundos de 11 indivíduos sadios. A expressão de CD44 foi positiva em 83 casos (76,8%) das leucemias linfóides agudas, sendo 46 casos (80,7%) das LLA de linhagem B. e em 37 casos (72,5%) de LLA de células-T. Nos quatro subgrupos que compõem as LLA de linhagem B, observamos a expressão desta molécula em dois casos (66,7%) das LLA do tipo nuli; em 34 casos (77.3%) das LLA do tipo comum e em todos os casos de LLA pré-B (cµ+) e LLA-B (Smlg+). Já nas LLA de células-T. a expressão do CD44 mostrou-se variável nos três subgrupos que compõem estas leucemias. No Subgrupo 1 (LLA pré-T), todos os nove casos (100%) foram CD44 positivos; nos 14 casos do Subgrupo II (LLA-T intermediária), quatro casos (28,6%) ftram CD44 positivos e no Subgrupo III (LLA-T-medular) o CD44 foi positivo em 24 casos (85.7%). A correlação da expressão de CD44 com o perfil clínico-patológico destas LLA, mostrou que a expressão desta molécula correlacionou-se com as leucemias que apresentavam formas tumorais da doença, traduzida pela presença de hepatomegalias, esplenomegalias, linfadenopatias e, principalmente, nos casos em que havia a presença de massas tumorais abdominais e de mediastino, assim como infiltração no sistema nervoso central, quando comparadas as leucemias com doença restrita ao sistema hematopoético. Com estes dados, nós sugerimos que o CD44 pode ser empregado como marcador adicional na monitorização da evolução prognóstica e para avaliação dos mecanismos de evolução patológica das leucemias linfoides agudas.INCA2022-09-27info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArtigos, Avaliado pelos paresapplication/pdfhttps://rbc.inca.gov.br/index.php/revista/article/view/283410.32635/2176-9745.RBC.1997v43n1.2834Revista Brasileira de Cancerologia; Vol. 43 No. 1 (1997): Jan./Feb./Mar.; 9-20Revista Brasileira de Cancerologia; Vol. 43 Núm. 1 (1997): ene./feb./mar.; 9-20Revista Brasileira de Cancerologia; v. 43 n. 1 (1997): jan./fev./mar.; 9-202176-9745reponame:Revista Brasileira de Cancerologia (Online)instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)instacron:INCAporhttps://rbc.inca.gov.br/index.php/revista/article/view/2834/1710https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessCavalcanti Júnior, Geraldo BarrosoSavino, WilsonMaia, Raquel CiuvalschiDobbin, Jane de AlmeidaCarriço, Maria KadmaHarab, Hansa CabralPombo de Oliveira, Maria do Socorro2023-01-18T14:48:26Zoai:rbc.inca.gov.br:article/2834Revistahttps://rbc.inca.gov.br/index.php/revistaPUBhttps://rbc.inca.gov.br/index.php/revista/oairbc@inca.gov.br0034-71162176-9745opendoar:2023-01-18T14:48:26Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)false |
dc.title.none.fl_str_mv |
Correlation between the cellular expression of CD44 and the forms of acute lymphoblastic leukemia Correlação entre a expressão celular do CD44 e formas tumorais das leucemias linfoblásticas |
title |
Correlation between the cellular expression of CD44 and the forms of acute lymphoblastic leukemia |
spellingShingle |
Correlation between the cellular expression of CD44 and the forms of acute lymphoblastic leukemia Cavalcanti Júnior, Geraldo Barroso Anticorpo Monoclonal CD44 Leucemia Linfóide Aguda CD44 Monoclonal Antibody Acute Lymphoid Leukemia |
title_short |
Correlation between the cellular expression of CD44 and the forms of acute lymphoblastic leukemia |
title_full |
Correlation between the cellular expression of CD44 and the forms of acute lymphoblastic leukemia |
title_fullStr |
Correlation between the cellular expression of CD44 and the forms of acute lymphoblastic leukemia |
title_full_unstemmed |
Correlation between the cellular expression of CD44 and the forms of acute lymphoblastic leukemia |
title_sort |
Correlation between the cellular expression of CD44 and the forms of acute lymphoblastic leukemia |
author |
Cavalcanti Júnior, Geraldo Barroso |
author_facet |
Cavalcanti Júnior, Geraldo Barroso Savino, Wilson Maia, Raquel Ciuvalschi Dobbin, Jane de Almeida Carriço, Maria Kadma Harab, Hansa Cabral Pombo de Oliveira, Maria do Socorro |
author_role |
author |
author2 |
Savino, Wilson Maia, Raquel Ciuvalschi Dobbin, Jane de Almeida Carriço, Maria Kadma Harab, Hansa Cabral Pombo de Oliveira, Maria do Socorro |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Cavalcanti Júnior, Geraldo Barroso Savino, Wilson Maia, Raquel Ciuvalschi Dobbin, Jane de Almeida Carriço, Maria Kadma Harab, Hansa Cabral Pombo de Oliveira, Maria do Socorro |
dc.subject.por.fl_str_mv |
Anticorpo Monoclonal CD44 Leucemia Linfóide Aguda CD44 Monoclonal Antibody Acute Lymphoid Leukemia |
topic |
Anticorpo Monoclonal CD44 Leucemia Linfóide Aguda CD44 Monoclonal Antibody Acute Lymphoid Leukemia |
description |
CD44 is an adhesion molecule expressed by B and T lymphocytes, that mediates cell attachment to extraceliular matrix componentes and adhesion to endothelial cells. The purpose of this study is to investigate the CD44 expression in 108 patients with lymphoblastic leukemia (57 B lineage ALL and 51 T-cell ALL) with a methodology that includes morphological analysis and immunophenotyping with a panel of monoclonal antibodies detected by standard techniques such as immunoperoxidase conjugated methods and flow-cytometry. lnitially we investigated the correlation of CD44 expression with all levels of cellular maturation of these leukemia, established according to antigen expression. Then, we investigated the correlation of this molecule with clinical-pathologic features such as mediastinal mass, adenomegaly and infiltration of the central nervous systein, and number of blastic cells in peripheral blood. In addition, we also investigated CD44 expression in peripheral lymphocytesfrom 11 healthy individuais. The CD44 expression was positive in 83 (76.8%) out of 108 ALL cases studied. In B precursors and B-ALL its expression was observed in 46 (80.8%) out of 57 cases and 37(72.5%) out of 51 cases of T-ALL. In the four subgroups of B precursor ALL, the expression of this molecule was found in 2 cases (66.7%) of null-ALL, in 34 cases (73.5%) of C-ALL and al cases of pre-B (cµ+) and B-ALL (Smlg+). Considering, T-cell ALL, the CD44 expression was variable among the three subgroups of this leukemia. In Subgroup 1 (pre-TALL) all 9 cases were positive (100%). In 14 Subgroups 11 (intermediate T-cell ALL) CD44 was positive in 4 cases (28.6%) and amongst the 28 cases of Subgroup III, CD44 was positive in 24 cases (85.7%). In lymphocytes from the control groups, CD44 expression was positive in all cases with percentages of reactivity ranging from 80% to 100% of cases, which homogeneously exhibited high density of CD44, as assessed by cytofluorimetrv. The correlation of CD44 expression in terms of clinical-pathologic profile o fALL demonstrated that high levels of CD44 were associated to tumoral forms of disease expressed as lymphadenopathy, hepatomegaly, splenomegaly, tumoral masses and infiltration of central nervous system. However, we did not find any association between CD44 and high leveis of circulating blast cells. These data suggest that CD44 should be considered au addicional marker to monitor evolution and asses the mechanisms of pathological evolution of the lvmphohlastic leukemia. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-09-27 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Artigos, Avaliado pelos pares |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rbc.inca.gov.br/index.php/revista/article/view/2834 10.32635/2176-9745.RBC.1997v43n1.2834 |
url |
https://rbc.inca.gov.br/index.php/revista/article/view/2834 |
identifier_str_mv |
10.32635/2176-9745.RBC.1997v43n1.2834 |
dc.language.iso.fl_str_mv |
por |
language |
por |
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https://rbc.inca.gov.br/index.php/revista/article/view/2834/1710 |
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https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
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https://creativecommons.org/licenses/by/4.0 |
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openAccess |
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INCA |
publisher.none.fl_str_mv |
INCA |
dc.source.none.fl_str_mv |
Revista Brasileira de Cancerologia; Vol. 43 No. 1 (1997): Jan./Feb./Mar.; 9-20 Revista Brasileira de Cancerologia; Vol. 43 Núm. 1 (1997): ene./feb./mar.; 9-20 Revista Brasileira de Cancerologia; v. 43 n. 1 (1997): jan./fev./mar.; 9-20 2176-9745 reponame:Revista Brasileira de Cancerologia (Online) instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) instacron:INCA |
instname_str |
Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) |
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INCA |
institution |
INCA |
reponame_str |
Revista Brasileira de Cancerologia (Online) |
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Revista Brasileira de Cancerologia (Online) |
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Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) |
repository.mail.fl_str_mv |
rbc@inca.gov.br |
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