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Circulating RNA biomarkers in diffuse large B-cell lymphoma: a systematic review

Diffuse large B-cell lymphoma (DLBCL) is the most common histological subtype of non-Hodgkin’s lymphomas (NHL). DLBCL is an aggressive malignancy that displays a great heterogeneity in terms of morphology, genetics and biological behavior. While a sustained complete remission is obtained in the majo...

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Autores principales: Decruyenaere, Philippe, Offner, Fritz, Vandesompele, Jo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885416/
https://www.ncbi.nlm.nih.gov/pubmed/33593440
http://dx.doi.org/10.1186/s40164-021-00208-3
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author Decruyenaere, Philippe
Offner, Fritz
Vandesompele, Jo
author_facet Decruyenaere, Philippe
Offner, Fritz
Vandesompele, Jo
author_sort Decruyenaere, Philippe
collection PubMed
description Diffuse large B-cell lymphoma (DLBCL) is the most common histological subtype of non-Hodgkin’s lymphomas (NHL). DLBCL is an aggressive malignancy that displays a great heterogeneity in terms of morphology, genetics and biological behavior. While a sustained complete remission is obtained in the majority of patients with standard immunochemotherapy, patients with refractory of relapsed disease after first-line treatment have a poor prognosis. This patient group represents an important unmet need in lymphoma treatment. In recent years, improved understanding of the underlying molecular pathogenesis had led to new classification and prognostication tools, including the development of cell-free biomarkers in liquid biopsies. Although the majority of studies have focused on the use of cell-free fragments of DNA (cfDNA), there has been an increased interest in circulating-free coding and non-coding RNA, including messenger RNA (mRNA), microRNA (miRNA), long non-coding RNA (lncRNA) and circular RNA (circRNA), as well as RNA encapsulated in extracellular vesicles or tumor-educated platelets (TEPs). We performed a systematic search in PubMed to identify articles that evaluated circulating RNA as diagnostic, subtype, treatment response or prognostic biomarkers in a human DLBCL population. A total of 35 articles met the inclusion criteria. The aim of this systematic review is to present the current understanding of circulating RNA molecules as biomarker in DLBCL and to discuss their future potential.
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spelling pubmed-78854162021-02-17 Circulating RNA biomarkers in diffuse large B-cell lymphoma: a systematic review Decruyenaere, Philippe Offner, Fritz Vandesompele, Jo Exp Hematol Oncol Review Diffuse large B-cell lymphoma (DLBCL) is the most common histological subtype of non-Hodgkin’s lymphomas (NHL). DLBCL is an aggressive malignancy that displays a great heterogeneity in terms of morphology, genetics and biological behavior. While a sustained complete remission is obtained in the majority of patients with standard immunochemotherapy, patients with refractory of relapsed disease after first-line treatment have a poor prognosis. This patient group represents an important unmet need in lymphoma treatment. In recent years, improved understanding of the underlying molecular pathogenesis had led to new classification and prognostication tools, including the development of cell-free biomarkers in liquid biopsies. Although the majority of studies have focused on the use of cell-free fragments of DNA (cfDNA), there has been an increased interest in circulating-free coding and non-coding RNA, including messenger RNA (mRNA), microRNA (miRNA), long non-coding RNA (lncRNA) and circular RNA (circRNA), as well as RNA encapsulated in extracellular vesicles or tumor-educated platelets (TEPs). We performed a systematic search in PubMed to identify articles that evaluated circulating RNA as diagnostic, subtype, treatment response or prognostic biomarkers in a human DLBCL population. A total of 35 articles met the inclusion criteria. The aim of this systematic review is to present the current understanding of circulating RNA molecules as biomarker in DLBCL and to discuss their future potential. BioMed Central 2021-02-16 /pmc/articles/PMC7885416/ /pubmed/33593440 http://dx.doi.org/10.1186/s40164-021-00208-3 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Decruyenaere, Philippe
Offner, Fritz
Vandesompele, Jo
Circulating RNA biomarkers in diffuse large B-cell lymphoma: a systematic review
title Circulating RNA biomarkers in diffuse large B-cell lymphoma: a systematic review
title_full Circulating RNA biomarkers in diffuse large B-cell lymphoma: a systematic review
title_fullStr Circulating RNA biomarkers in diffuse large B-cell lymphoma: a systematic review
title_full_unstemmed Circulating RNA biomarkers in diffuse large B-cell lymphoma: a systematic review
title_short Circulating RNA biomarkers in diffuse large B-cell lymphoma: a systematic review
title_sort circulating rna biomarkers in diffuse large b-cell lymphoma: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885416/
https://www.ncbi.nlm.nih.gov/pubmed/33593440
http://dx.doi.org/10.1186/s40164-021-00208-3
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