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Evaluation of diagnostic efficacy of NRP‐1/CD304 in hematological diseases
BACKGROUND: Previous studies had explored the diagnostic or prognostic value of NRP‐1/CD304 in blastic plasmacytoid dendritic cell neoplasm (BPDCN), acute myeloid leukemia (AML), and B‐cell acute lymphoblastic leukemia (B‐ALL), whereas the expression and application value of NRP‐1/CD304 in other com...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242364/ https://www.ncbi.nlm.nih.gov/pubmed/36965095 http://dx.doi.org/10.1002/cam4.5838 |
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author | Liu, Yi‐jun Li, Xiao‐hui Song, Yi‐ling Zhou, Yi‐chen Cai, Rong‐zeng Chi, Pei‐dong |
author_facet | Liu, Yi‐jun Li, Xiao‐hui Song, Yi‐ling Zhou, Yi‐chen Cai, Rong‐zeng Chi, Pei‐dong |
author_sort | Liu, Yi‐jun |
collection | PubMed |
description | BACKGROUND: Previous studies had explored the diagnostic or prognostic value of NRP‐1/CD304 in blastic plasmacytoid dendritic cell neoplasm (BPDCN), acute myeloid leukemia (AML), and B‐cell acute lymphoblastic leukemia (B‐ALL), whereas the expression and application value of NRP‐1/CD304 in other common hematological diseases have not been reported. METHODS: Bone marrow samples from 297 newly diagnosed patients with various hematological diseases were collected to detect the expression of NRP‐1/CD304 by flow cytometry (FCM). The diagnostic efficacy of NRP‐1/ CD304‐positive diseases was analyzed by receiver operating characteristic (ROC) curve, and the area under the ROC curve (AUC) was compared. RESULTS: In the research cohort, the total positive rate of NRP‐1/CD304 was 14.81% (44/297), mainly distributed in BPDCN (100%, 6/6), B‐ALL (48.61%, 35/72), and AML (4.48%, 3/67), with statistically significant differences (p < 0.01). Other diseases, such as T‐cell acute lymphoblastic leukemia (T‐ALL), B‐cell non‐Hodgkin lymphoma (B‐NHL), T/NK‐cell lymphoma and plasma cell neoplasms, did not express NRP‐1/CD304. The AUC of NRP‐1/CD304 was 0.936 (95% CI 0.898–0.973), 0.723 (95% CI 0.646–0.801), and 0.435 (95% CI 0.435) in BPDCN, B‐ALL and AML, respectively. Besides, CD304 was commonly expressed in B‐ALL with BCR‐ABL1 gene rearrangement (p = 0.000), and CD304 expression was positively correlated with CD34 co‐expression (p = 0.009) and CD10 co‐expression (p = 0.007). CONCLUSIONS: NRP‐1/CD304 is only expressed in BPDCN, B‐ALL and AML, but not in other common hematological diseases. This indicates that NRP‐1/CD304 has no obvious diagnostic and follow‐up study value in hematological diseases other than BPDCN, B‐ALL, and AML. |
format | Online Article Text |
id | pubmed-10242364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102423642023-06-07 Evaluation of diagnostic efficacy of NRP‐1/CD304 in hematological diseases Liu, Yi‐jun Li, Xiao‐hui Song, Yi‐ling Zhou, Yi‐chen Cai, Rong‐zeng Chi, Pei‐dong Cancer Med RESEARCH ARTICLES BACKGROUND: Previous studies had explored the diagnostic or prognostic value of NRP‐1/CD304 in blastic plasmacytoid dendritic cell neoplasm (BPDCN), acute myeloid leukemia (AML), and B‐cell acute lymphoblastic leukemia (B‐ALL), whereas the expression and application value of NRP‐1/CD304 in other common hematological diseases have not been reported. METHODS: Bone marrow samples from 297 newly diagnosed patients with various hematological diseases were collected to detect the expression of NRP‐1/CD304 by flow cytometry (FCM). The diagnostic efficacy of NRP‐1/ CD304‐positive diseases was analyzed by receiver operating characteristic (ROC) curve, and the area under the ROC curve (AUC) was compared. RESULTS: In the research cohort, the total positive rate of NRP‐1/CD304 was 14.81% (44/297), mainly distributed in BPDCN (100%, 6/6), B‐ALL (48.61%, 35/72), and AML (4.48%, 3/67), with statistically significant differences (p < 0.01). Other diseases, such as T‐cell acute lymphoblastic leukemia (T‐ALL), B‐cell non‐Hodgkin lymphoma (B‐NHL), T/NK‐cell lymphoma and plasma cell neoplasms, did not express NRP‐1/CD304. The AUC of NRP‐1/CD304 was 0.936 (95% CI 0.898–0.973), 0.723 (95% CI 0.646–0.801), and 0.435 (95% CI 0.435) in BPDCN, B‐ALL and AML, respectively. Besides, CD304 was commonly expressed in B‐ALL with BCR‐ABL1 gene rearrangement (p = 0.000), and CD304 expression was positively correlated with CD34 co‐expression (p = 0.009) and CD10 co‐expression (p = 0.007). CONCLUSIONS: NRP‐1/CD304 is only expressed in BPDCN, B‐ALL and AML, but not in other common hematological diseases. This indicates that NRP‐1/CD304 has no obvious diagnostic and follow‐up study value in hematological diseases other than BPDCN, B‐ALL, and AML. John Wiley and Sons Inc. 2023-03-25 /pmc/articles/PMC10242364/ /pubmed/36965095 http://dx.doi.org/10.1002/cam4.5838 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RESEARCH ARTICLES Liu, Yi‐jun Li, Xiao‐hui Song, Yi‐ling Zhou, Yi‐chen Cai, Rong‐zeng Chi, Pei‐dong Evaluation of diagnostic efficacy of NRP‐1/CD304 in hematological diseases |
title | Evaluation of diagnostic efficacy of NRP‐1/CD304 in hematological diseases |
title_full | Evaluation of diagnostic efficacy of NRP‐1/CD304 in hematological diseases |
title_fullStr | Evaluation of diagnostic efficacy of NRP‐1/CD304 in hematological diseases |
title_full_unstemmed | Evaluation of diagnostic efficacy of NRP‐1/CD304 in hematological diseases |
title_short | Evaluation of diagnostic efficacy of NRP‐1/CD304 in hematological diseases |
title_sort | evaluation of diagnostic efficacy of nrp‐1/cd304 in hematological diseases |
topic | RESEARCH ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242364/ https://www.ncbi.nlm.nih.gov/pubmed/36965095 http://dx.doi.org/10.1002/cam4.5838 |
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