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Characterization of clonal immunoglobulin heavy V-D-J gene rearrangements in Chinese patients with chronic lymphocytic leukemia: Clinical features and molecular profiles

INTRODUCTION: Several prognostic factors of chronic lymphocytic leukemia (CLL) have been identified, such as cytogenetic aberrations and recurrent gene mutations. B-cell receptor (BCR) signaling plays an important role in the tumorigenesis of CLL, and its clinical significance in predicting prognosi...

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Autores principales: Deng, Xinyue, Zhang, Meilan, Wang, Jiachen, Zhou, Xiaoxi, Xiao, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9978106/
https://www.ncbi.nlm.nih.gov/pubmed/36874132
http://dx.doi.org/10.3389/fonc.2023.1120867
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author Deng, Xinyue
Zhang, Meilan
Wang, Jiachen
Zhou, Xiaoxi
Xiao, Min
author_facet Deng, Xinyue
Zhang, Meilan
Wang, Jiachen
Zhou, Xiaoxi
Xiao, Min
author_sort Deng, Xinyue
collection PubMed
description INTRODUCTION: Several prognostic factors of chronic lymphocytic leukemia (CLL) have been identified, such as cytogenetic aberrations and recurrent gene mutations. B-cell receptor (BCR) signaling plays an important role in the tumorigenesis of CLL, and its clinical significance in predicting prognosis is also under study. METHODS: Therefore, we assessed the already-known prognostic markers, immunoglobulin heavy chain (IGH) gene usage and the associations among these factors in 71 patients diagnosed with CLL in our center from October 2017 to March 2022. Sequencing of IGH gene rearrangements was performed using Sanger sequencing or IGH-based next-generation sequencing, and the results were further analyzed for distinct IGH/IGHD/IGHJ genes and the mutational status of the clonotypic IGHV (IGH variable) gene. RESULTS: In summary, by analyzing the distribution of potential prognostic factors in CLL patients, we displayed a landscape of molecular profiles, confirmed the predictive value of recurrent genetic mutations and chromosome aberrations, and found that IGHJ3 was associated with favorable markers (mutated IGHV, trisomy 12), while IGHJ6 tended to correlate with unfavorable factors (unmutated IGHV, del17p). DISCUSSION: These results provided an indication for IGH gene sequencing in predicting the prognosis of CLL.
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spelling pubmed-99781062023-03-03 Characterization of clonal immunoglobulin heavy V-D-J gene rearrangements in Chinese patients with chronic lymphocytic leukemia: Clinical features and molecular profiles Deng, Xinyue Zhang, Meilan Wang, Jiachen Zhou, Xiaoxi Xiao, Min Front Oncol Oncology INTRODUCTION: Several prognostic factors of chronic lymphocytic leukemia (CLL) have been identified, such as cytogenetic aberrations and recurrent gene mutations. B-cell receptor (BCR) signaling plays an important role in the tumorigenesis of CLL, and its clinical significance in predicting prognosis is also under study. METHODS: Therefore, we assessed the already-known prognostic markers, immunoglobulin heavy chain (IGH) gene usage and the associations among these factors in 71 patients diagnosed with CLL in our center from October 2017 to March 2022. Sequencing of IGH gene rearrangements was performed using Sanger sequencing or IGH-based next-generation sequencing, and the results were further analyzed for distinct IGH/IGHD/IGHJ genes and the mutational status of the clonotypic IGHV (IGH variable) gene. RESULTS: In summary, by analyzing the distribution of potential prognostic factors in CLL patients, we displayed a landscape of molecular profiles, confirmed the predictive value of recurrent genetic mutations and chromosome aberrations, and found that IGHJ3 was associated with favorable markers (mutated IGHV, trisomy 12), while IGHJ6 tended to correlate with unfavorable factors (unmutated IGHV, del17p). DISCUSSION: These results provided an indication for IGH gene sequencing in predicting the prognosis of CLL. Frontiers Media S.A. 2023-02-16 /pmc/articles/PMC9978106/ /pubmed/36874132 http://dx.doi.org/10.3389/fonc.2023.1120867 Text en Copyright © 2023 Deng, Zhang, Wang, Zhou and Xiao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Deng, Xinyue
Zhang, Meilan
Wang, Jiachen
Zhou, Xiaoxi
Xiao, Min
Characterization of clonal immunoglobulin heavy V-D-J gene rearrangements in Chinese patients with chronic lymphocytic leukemia: Clinical features and molecular profiles
title Characterization of clonal immunoglobulin heavy V-D-J gene rearrangements in Chinese patients with chronic lymphocytic leukemia: Clinical features and molecular profiles
title_full Characterization of clonal immunoglobulin heavy V-D-J gene rearrangements in Chinese patients with chronic lymphocytic leukemia: Clinical features and molecular profiles
title_fullStr Characterization of clonal immunoglobulin heavy V-D-J gene rearrangements in Chinese patients with chronic lymphocytic leukemia: Clinical features and molecular profiles
title_full_unstemmed Characterization of clonal immunoglobulin heavy V-D-J gene rearrangements in Chinese patients with chronic lymphocytic leukemia: Clinical features and molecular profiles
title_short Characterization of clonal immunoglobulin heavy V-D-J gene rearrangements in Chinese patients with chronic lymphocytic leukemia: Clinical features and molecular profiles
title_sort characterization of clonal immunoglobulin heavy v-d-j gene rearrangements in chinese patients with chronic lymphocytic leukemia: clinical features and molecular profiles
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9978106/
https://www.ncbi.nlm.nih.gov/pubmed/36874132
http://dx.doi.org/10.3389/fonc.2023.1120867
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