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Genetic methylation and lymphoid malignancies: biomarkers of tumor progression and targeted therapy

Lymphoid malignancies, mainly including lymphocytic leukemia and lymphoma, are a group of heterogeneous diseases. Although the clinical outcome of patients has been significantly improved with current immuno-chemotherapy, definitive biomarkers remain to be investigated, particularly those reflecting...

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Detalles Bibliográficos
Autores principales: Zhao, Xia, Zhang, Wei, Wang, Li, Zhao, Wei-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101819/
https://www.ncbi.nlm.nih.gov/pubmed/24252620
http://dx.doi.org/10.1186/2050-7771-1-24
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author Zhao, Xia
Zhang, Wei
Wang, Li
Zhao, Wei-Li
author_facet Zhao, Xia
Zhang, Wei
Wang, Li
Zhao, Wei-Li
author_sort Zhao, Xia
collection PubMed
description Lymphoid malignancies, mainly including lymphocytic leukemia and lymphoma, are a group of heterogeneous diseases. Although the clinical outcome of patients has been significantly improved with current immuno-chemotherapy, definitive biomarkers remain to be investigated, particularly those reflecting the malignant behavior of tumor cells and those helpful for developing optimal targeted therapy. Recently, genome-wide analysis reveals that altered genetic methylations play an important role in tumor progression through regulation of multiple cellular transduction pathways. This review describes the pathogenetic effect of the aberrant genetic methylation in lymphoid malignancies, with special emphasis on potential therapeutic strategies targeting key signaling networks.
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spelling pubmed-41018192014-07-18 Genetic methylation and lymphoid malignancies: biomarkers of tumor progression and targeted therapy Zhao, Xia Zhang, Wei Wang, Li Zhao, Wei-Li Biomark Res Review Lymphoid malignancies, mainly including lymphocytic leukemia and lymphoma, are a group of heterogeneous diseases. Although the clinical outcome of patients has been significantly improved with current immuno-chemotherapy, definitive biomarkers remain to be investigated, particularly those reflecting the malignant behavior of tumor cells and those helpful for developing optimal targeted therapy. Recently, genome-wide analysis reveals that altered genetic methylations play an important role in tumor progression through regulation of multiple cellular transduction pathways. This review describes the pathogenetic effect of the aberrant genetic methylation in lymphoid malignancies, with special emphasis on potential therapeutic strategies targeting key signaling networks. BioMed Central 2013-08-14 /pmc/articles/PMC4101819/ /pubmed/24252620 http://dx.doi.org/10.1186/2050-7771-1-24 Text en Copyright © 2013 Zhao et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Zhao, Xia
Zhang, Wei
Wang, Li
Zhao, Wei-Li
Genetic methylation and lymphoid malignancies: biomarkers of tumor progression and targeted therapy
title Genetic methylation and lymphoid malignancies: biomarkers of tumor progression and targeted therapy
title_full Genetic methylation and lymphoid malignancies: biomarkers of tumor progression and targeted therapy
title_fullStr Genetic methylation and lymphoid malignancies: biomarkers of tumor progression and targeted therapy
title_full_unstemmed Genetic methylation and lymphoid malignancies: biomarkers of tumor progression and targeted therapy
title_short Genetic methylation and lymphoid malignancies: biomarkers of tumor progression and targeted therapy
title_sort genetic methylation and lymphoid malignancies: biomarkers of tumor progression and targeted therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101819/
https://www.ncbi.nlm.nih.gov/pubmed/24252620
http://dx.doi.org/10.1186/2050-7771-1-24
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