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Rapid identification of novel independent serum biomarkers in diffuse large B-cell lymphoma
BACKGROUND: Diffuse large B-cell lymphoma (DLBCL) is a common subtype of non-Hodgkin’s lymphoma (NHL). We assessed serum biomarkers to identify patients with DLBCL and healthy controls, as well as prognosis-related paired pre- and post-R-CHOP therapy effect of patients with DLBCL. METHODS: Serum sam...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797442/ https://www.ncbi.nlm.nih.gov/pubmed/35117818 http://dx.doi.org/10.21037/tcr-19-2809 |
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author | Che, Yi-Qun Wang, Di Liu, Peng Zhang, Yue Luo, Yang Liu, Hui-Ying Shen, Di Cui, Wei |
author_facet | Che, Yi-Qun Wang, Di Liu, Peng Zhang, Yue Luo, Yang Liu, Hui-Ying Shen, Di Cui, Wei |
author_sort | Che, Yi-Qun |
collection | PubMed |
description | BACKGROUND: Diffuse large B-cell lymphoma (DLBCL) is a common subtype of non-Hodgkin’s lymphoma (NHL). We assessed serum biomarkers to identify patients with DLBCL and healthy controls, as well as prognosis-related paired pre- and post-R-CHOP therapy effect of patients with DLBCL. METHODS: Serum samples from 329 DLBCL patients and 100 healthy controls were collected in this study, as well as 72 samples from additional DLBCL patients with paired pre- and post-R-CHOP therapy (n=36). All serum samples were pretreated and detected by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS). Serum biomarkers were discriminated between DLBCL patients and healthy controls, as well as between DLBCL patients with prognosis-related paired pre- and post-R-CHOP therapy, and identified by Veristrat Identification Platform 1.0, Bioyong Explore 1.0 and mMass software. RESULTS: Two peaks, m/z values of 15,140.74 and 15,885.43, were significantly different from all peaks among the DLBCL patients and healthy controls (P<0.001). Patients with DLBCL could be identified with a sensitivity of 85.9% and specificity of 91.8% of 15,140.74, in the same way for the sensitivity of 92.1% and specificity of 84.4% of 15,885.43. The m/z values of 13,895.80 were downregulated after R-CHOP treatment in DLBCL patients who obtained complete remission (CR) (P=0.018). CONCLUSIONS: The potential independent serum biomarkers for diagnosis as well as prognosis of DLBCL could be provided for rapid identification. |
format | Online Article Text |
id | pubmed-8797442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87974422022-02-02 Rapid identification of novel independent serum biomarkers in diffuse large B-cell lymphoma Che, Yi-Qun Wang, Di Liu, Peng Zhang, Yue Luo, Yang Liu, Hui-Ying Shen, Di Cui, Wei Transl Cancer Res Original Article BACKGROUND: Diffuse large B-cell lymphoma (DLBCL) is a common subtype of non-Hodgkin’s lymphoma (NHL). We assessed serum biomarkers to identify patients with DLBCL and healthy controls, as well as prognosis-related paired pre- and post-R-CHOP therapy effect of patients with DLBCL. METHODS: Serum samples from 329 DLBCL patients and 100 healthy controls were collected in this study, as well as 72 samples from additional DLBCL patients with paired pre- and post-R-CHOP therapy (n=36). All serum samples were pretreated and detected by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS). Serum biomarkers were discriminated between DLBCL patients and healthy controls, as well as between DLBCL patients with prognosis-related paired pre- and post-R-CHOP therapy, and identified by Veristrat Identification Platform 1.0, Bioyong Explore 1.0 and mMass software. RESULTS: Two peaks, m/z values of 15,140.74 and 15,885.43, were significantly different from all peaks among the DLBCL patients and healthy controls (P<0.001). Patients with DLBCL could be identified with a sensitivity of 85.9% and specificity of 91.8% of 15,140.74, in the same way for the sensitivity of 92.1% and specificity of 84.4% of 15,885.43. The m/z values of 13,895.80 were downregulated after R-CHOP treatment in DLBCL patients who obtained complete remission (CR) (P=0.018). CONCLUSIONS: The potential independent serum biomarkers for diagnosis as well as prognosis of DLBCL could be provided for rapid identification. AME Publishing Company 2020-08 /pmc/articles/PMC8797442/ /pubmed/35117818 http://dx.doi.org/10.21037/tcr-19-2809 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Original Article Che, Yi-Qun Wang, Di Liu, Peng Zhang, Yue Luo, Yang Liu, Hui-Ying Shen, Di Cui, Wei Rapid identification of novel independent serum biomarkers in diffuse large B-cell lymphoma |
title | Rapid identification of novel independent serum biomarkers in diffuse large B-cell lymphoma |
title_full | Rapid identification of novel independent serum biomarkers in diffuse large B-cell lymphoma |
title_fullStr | Rapid identification of novel independent serum biomarkers in diffuse large B-cell lymphoma |
title_full_unstemmed | Rapid identification of novel independent serum biomarkers in diffuse large B-cell lymphoma |
title_short | Rapid identification of novel independent serum biomarkers in diffuse large B-cell lymphoma |
title_sort | rapid identification of novel independent serum biomarkers in diffuse large b-cell lymphoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797442/ https://www.ncbi.nlm.nih.gov/pubmed/35117818 http://dx.doi.org/10.21037/tcr-19-2809 |
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