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Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes
Background and Aim. We studied through flow cytometry the expression of CD146 on different T cells, and B-cell ALL blasts trying to correlate its expression with different prognostic factors of B-cell ALL and treatment outcomes. Patients and Methods. All pediatric patients with B-cell ALL were subje...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031726/ https://www.ncbi.nlm.nih.gov/pubmed/32090132 http://dx.doi.org/10.1155/2020/9736159 |
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author | Zahran, Asmaa M. El-Badawy, Omnia Elsayh, Khalid I. Mohamed, Wael M. Y. Riad, Khalid F. Abdel-Rahim, Mona H. Rayan, Amal |
author_facet | Zahran, Asmaa M. El-Badawy, Omnia Elsayh, Khalid I. Mohamed, Wael M. Y. Riad, Khalid F. Abdel-Rahim, Mona H. Rayan, Amal |
author_sort | Zahran, Asmaa M. |
collection | PubMed |
description | Background and Aim. We studied through flow cytometry the expression of CD146 on different T cells, and B-cell ALL blasts trying to correlate its expression with different prognostic factors of B-cell ALL and treatment outcomes. Patients and Methods. All pediatric patients with B-cell ALL were subjected to bone marrow examination and cytochemistry, flow cytometric immunophenotyping using monoclonal antibodies utilized for diagnosis of B-ALL including CD34, CD19, CD10, CD22, and intracellular IgM. The diagnosis was based on standard morphologic, cytochemical, and immunophenotypic followed by flow cytometric detection of CD146 expression on blast cells, CD4(+), and CD8(+) T cells. RESULTS: Significant accumulations of CD146(+)CD4(+) cells, CD146(+)CD8(+) cells, CD4(+), CD8(+), and lymphocytes in patients were compared to controls, the mean percentages of CD146(+)CD4(+) cells, CD146(+)CD8(+) cells, and CD146(+) blasts were significantly higher in patients than controls, and in addition, these cells were associated with poor overall survival and disease-free survival. The median OS for patients with complete response was 22 ± 1.633 (95%CI = 18.799‐25.201), while for those without complete response, it was 13 ± 3.928 (95%CI = 5.301‐25.699), with log‐rank = 5.71, P = 0.017. CONCLUSION: CD146 was expressed significantly in children's B-ALL and associated with poor prognostic features including poor response and treatment outcomes and could be a possible poor prognostic factor in pediatric B-cell ALL. |
format | Online Article Text |
id | pubmed-7031726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-70317262020-02-21 Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes Zahran, Asmaa M. El-Badawy, Omnia Elsayh, Khalid I. Mohamed, Wael M. Y. Riad, Khalid F. Abdel-Rahim, Mona H. Rayan, Amal J Immunol Res Research Article Background and Aim. We studied through flow cytometry the expression of CD146 on different T cells, and B-cell ALL blasts trying to correlate its expression with different prognostic factors of B-cell ALL and treatment outcomes. Patients and Methods. All pediatric patients with B-cell ALL were subjected to bone marrow examination and cytochemistry, flow cytometric immunophenotyping using monoclonal antibodies utilized for diagnosis of B-ALL including CD34, CD19, CD10, CD22, and intracellular IgM. The diagnosis was based on standard morphologic, cytochemical, and immunophenotypic followed by flow cytometric detection of CD146 expression on blast cells, CD4(+), and CD8(+) T cells. RESULTS: Significant accumulations of CD146(+)CD4(+) cells, CD146(+)CD8(+) cells, CD4(+), CD8(+), and lymphocytes in patients were compared to controls, the mean percentages of CD146(+)CD4(+) cells, CD146(+)CD8(+) cells, and CD146(+) blasts were significantly higher in patients than controls, and in addition, these cells were associated with poor overall survival and disease-free survival. The median OS for patients with complete response was 22 ± 1.633 (95%CI = 18.799‐25.201), while for those without complete response, it was 13 ± 3.928 (95%CI = 5.301‐25.699), with log‐rank = 5.71, P = 0.017. CONCLUSION: CD146 was expressed significantly in children's B-ALL and associated with poor prognostic features including poor response and treatment outcomes and could be a possible poor prognostic factor in pediatric B-cell ALL. Hindawi 2020-02-08 /pmc/articles/PMC7031726/ /pubmed/32090132 http://dx.doi.org/10.1155/2020/9736159 Text en Copyright © 2020 Asmaa M. Zahran et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zahran, Asmaa M. El-Badawy, Omnia Elsayh, Khalid I. Mohamed, Wael M. Y. Riad, Khalid F. Abdel-Rahim, Mona H. Rayan, Amal Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes |
title | Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes |
title_full | Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes |
title_fullStr | Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes |
title_full_unstemmed | Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes |
title_short | Upregulation of CD146 in Pediatric B-Cell Acute Lymphocytic Leukemia and Its Implications on Treatment Outcomes |
title_sort | upregulation of cd146 in pediatric b-cell acute lymphocytic leukemia and its implications on treatment outcomes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031726/ https://www.ncbi.nlm.nih.gov/pubmed/32090132 http://dx.doi.org/10.1155/2020/9736159 |
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