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MicroRNA and gene networks in human diffuse large B-cell lymphoma

Molecular biologists have collected considerable data regarding the involvement of genes and microRNAs (miRNAs) in cancer. However the underlying mechanisms of cancer with regard to genes and miRNAs remain unclear. The aim of the present study was to evaluate diffuse large B-cell lymphoma (DLBCL) an...

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Autores principales: WANG, KUNHAO, XU, ZHIWEN, WANG, NING, XU, TING, ZHU, MINGHUI
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4186561/
https://www.ncbi.nlm.nih.gov/pubmed/25289101
http://dx.doi.org/10.3892/ol.2014.2438
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author WANG, KUNHAO
XU, ZHIWEN
WANG, NING
XU, TING
ZHU, MINGHUI
author_facet WANG, KUNHAO
XU, ZHIWEN
WANG, NING
XU, TING
ZHU, MINGHUI
author_sort WANG, KUNHAO
collection PubMed
description Molecular biologists have collected considerable data regarding the involvement of genes and microRNAs (miRNAs) in cancer. However the underlying mechanisms of cancer with regard to genes and miRNAs remain unclear. The aim of the present study was to evaluate diffuse large B-cell lymphoma (DLBCL) and construct regulatory networks of genes and miRNAs to gradually reveal the underlying mechanisms of DLBCL development. The first differential expression network that is presented is an experimentally validated network of miRNAs and genes. This network presents known biological regulatory associations among miRNAs and genes in the human body. The second network is a DLBCL differential expression network. Differentially expressed gene and miRNA data regarding DLBCL were collected and, based on the first network and the differentially expressed data, the second network was inferred, which demonstrates the irregular regulatory associations that may lead to the occurrence of DLBCL. The third network is a DLBCL-associated network. This network is comprised of non-differentially expressed genes and miRNAs that contribute to numerous DLBCL processes. The similarities and differences among the three networks were extracted and compared to distinguish key regulatory associations; furthermore, important signaling pathways in DLBCL were identified. The present study partially clarified the pathogenesis of DLBCL and provided an improved understanding of the underlying molecular mechanisms, as well as a potential treatment for DLBCL.
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spelling pubmed-41865612014-10-06 MicroRNA and gene networks in human diffuse large B-cell lymphoma WANG, KUNHAO XU, ZHIWEN WANG, NING XU, TING ZHU, MINGHUI Oncol Lett Articles Molecular biologists have collected considerable data regarding the involvement of genes and microRNAs (miRNAs) in cancer. However the underlying mechanisms of cancer with regard to genes and miRNAs remain unclear. The aim of the present study was to evaluate diffuse large B-cell lymphoma (DLBCL) and construct regulatory networks of genes and miRNAs to gradually reveal the underlying mechanisms of DLBCL development. The first differential expression network that is presented is an experimentally validated network of miRNAs and genes. This network presents known biological regulatory associations among miRNAs and genes in the human body. The second network is a DLBCL differential expression network. Differentially expressed gene and miRNA data regarding DLBCL were collected and, based on the first network and the differentially expressed data, the second network was inferred, which demonstrates the irregular regulatory associations that may lead to the occurrence of DLBCL. The third network is a DLBCL-associated network. This network is comprised of non-differentially expressed genes and miRNAs that contribute to numerous DLBCL processes. The similarities and differences among the three networks were extracted and compared to distinguish key regulatory associations; furthermore, important signaling pathways in DLBCL were identified. The present study partially clarified the pathogenesis of DLBCL and provided an improved understanding of the underlying molecular mechanisms, as well as a potential treatment for DLBCL. D.A. Spandidos 2014-11 2014-08-12 /pmc/articles/PMC4186561/ /pubmed/25289101 http://dx.doi.org/10.3892/ol.2014.2438 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
WANG, KUNHAO
XU, ZHIWEN
WANG, NING
XU, TING
ZHU, MINGHUI
MicroRNA and gene networks in human diffuse large B-cell lymphoma
title MicroRNA and gene networks in human diffuse large B-cell lymphoma
title_full MicroRNA and gene networks in human diffuse large B-cell lymphoma
title_fullStr MicroRNA and gene networks in human diffuse large B-cell lymphoma
title_full_unstemmed MicroRNA and gene networks in human diffuse large B-cell lymphoma
title_short MicroRNA and gene networks in human diffuse large B-cell lymphoma
title_sort microrna and gene networks in human diffuse large b-cell lymphoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4186561/
https://www.ncbi.nlm.nih.gov/pubmed/25289101
http://dx.doi.org/10.3892/ol.2014.2438
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