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Clinically useful flow cytometry approach to identify immunophenotype in acute leukemia
OBJECTIVES: Acute leukemia (AL) is a highly heterogeneous malignant disease caused by hematopoietic cell abnormalities. Our study investigated the potential for immunophenotyping of leukemic cells via flow cytometry and the clinical usefulness of this approach in treatment of AL. METHODS: Bone marro...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6460589/ https://www.ncbi.nlm.nih.gov/pubmed/30614357 http://dx.doi.org/10.1177/0300060518819637 |
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author | Ouyang, Guifang Xu, Zhijuan Jiang, Danjie Zhu, Huiling Wang, Yi Wu, Wenmiao Sun, Yongcheng Sheng, Lixia Xu, Kaihong Lou, Yanru Mu, Qitian Zhang, Yi Wu, Ningning Cheng, Jia Duan, Shiwei |
author_facet | Ouyang, Guifang Xu, Zhijuan Jiang, Danjie Zhu, Huiling Wang, Yi Wu, Wenmiao Sun, Yongcheng Sheng, Lixia Xu, Kaihong Lou, Yanru Mu, Qitian Zhang, Yi Wu, Ningning Cheng, Jia Duan, Shiwei |
author_sort | Ouyang, Guifang |
collection | PubMed |
description | OBJECTIVES: Acute leukemia (AL) is a highly heterogeneous malignant disease caused by hematopoietic cell abnormalities. Our study investigated the potential for immunophenotyping of leukemic cells via flow cytometry and the clinical usefulness of this approach in treatment of AL. METHODS: Bone marrow (BM) specimens were collected to detect antigen expression on hematopoietic cells in pre-treatment samples from patients with AL. In addition, fraction survival curves were calculated using the Kaplan-Meier method to explore the effect of markers on prognosis in AL. RESULTS: Expression levels of immunophenotypic markers in patients with acute lymphoblastic leukemia (ALL) were significantly different from those in patients with acute myeloid leukemia (AML). In addition, there was a potential association between the surface marker, cluster of differentiation 2 (CD2), and fraction survival in AML. However, no similar result was found in ALL. Moreover, genetic tests showed greater positive variation of the break point cluster-Abelson tyrosine kinase (BCR-ABL) fusion gene in samples from patients with ALL than in samples from patients with AML. CONCLUSIONS: We have shown a rapid and effective flow cytometry method that enables the identification of immunophenotype in AL. Moreover, CD2 may constitute a predictive marker for prognosis in patients with AML. |
format | Online Article Text |
id | pubmed-6460589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-64605892019-04-19 Clinically useful flow cytometry approach to identify immunophenotype in acute leukemia Ouyang, Guifang Xu, Zhijuan Jiang, Danjie Zhu, Huiling Wang, Yi Wu, Wenmiao Sun, Yongcheng Sheng, Lixia Xu, Kaihong Lou, Yanru Mu, Qitian Zhang, Yi Wu, Ningning Cheng, Jia Duan, Shiwei J Int Med Res Clinical Research Reports OBJECTIVES: Acute leukemia (AL) is a highly heterogeneous malignant disease caused by hematopoietic cell abnormalities. Our study investigated the potential for immunophenotyping of leukemic cells via flow cytometry and the clinical usefulness of this approach in treatment of AL. METHODS: Bone marrow (BM) specimens were collected to detect antigen expression on hematopoietic cells in pre-treatment samples from patients with AL. In addition, fraction survival curves were calculated using the Kaplan-Meier method to explore the effect of markers on prognosis in AL. RESULTS: Expression levels of immunophenotypic markers in patients with acute lymphoblastic leukemia (ALL) were significantly different from those in patients with acute myeloid leukemia (AML). In addition, there was a potential association between the surface marker, cluster of differentiation 2 (CD2), and fraction survival in AML. However, no similar result was found in ALL. Moreover, genetic tests showed greater positive variation of the break point cluster-Abelson tyrosine kinase (BCR-ABL) fusion gene in samples from patients with ALL than in samples from patients with AML. CONCLUSIONS: We have shown a rapid and effective flow cytometry method that enables the identification of immunophenotype in AL. Moreover, CD2 may constitute a predictive marker for prognosis in patients with AML. SAGE Publications 2019-01-07 2019-04 /pmc/articles/PMC6460589/ /pubmed/30614357 http://dx.doi.org/10.1177/0300060518819637 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Clinical Research Reports Ouyang, Guifang Xu, Zhijuan Jiang, Danjie Zhu, Huiling Wang, Yi Wu, Wenmiao Sun, Yongcheng Sheng, Lixia Xu, Kaihong Lou, Yanru Mu, Qitian Zhang, Yi Wu, Ningning Cheng, Jia Duan, Shiwei Clinically useful flow cytometry approach to identify immunophenotype in acute leukemia |
title | Clinically useful flow cytometry approach to identify immunophenotype in acute leukemia |
title_full | Clinically useful flow cytometry approach to identify immunophenotype in acute leukemia |
title_fullStr | Clinically useful flow cytometry approach to identify immunophenotype in acute leukemia |
title_full_unstemmed | Clinically useful flow cytometry approach to identify immunophenotype in acute leukemia |
title_short | Clinically useful flow cytometry approach to identify immunophenotype in acute leukemia |
title_sort | clinically useful flow cytometry approach to identify immunophenotype in acute leukemia |
topic | Clinical Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6460589/ https://www.ncbi.nlm.nih.gov/pubmed/30614357 http://dx.doi.org/10.1177/0300060518819637 |
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