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Gene expression of WWOX, FHIT and p73 in acute lymphoblastic leukemia

The aim of the present study was to analyze the expression of WW-domain oxidoreductase (WWOX), fragile histidine triad (FHIT) and p73 in acute lymphoblastic leukemia (ALL). Samples from 122 ALL patients and 35 non-ALL control patients were collected in this study. RT-PCR was performed to detect the...

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Autores principales: CHEN, XU, ZHANG, HUI, LI, PING, YANG, ZHENG, QIN, LINGYAN, MO, WUNING
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3796419/
https://www.ncbi.nlm.nih.gov/pubmed/24137446
http://dx.doi.org/10.3892/ol.2013.1514
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author CHEN, XU
ZHANG, HUI
LI, PING
YANG, ZHENG
QIN, LINGYAN
MO, WUNING
author_facet CHEN, XU
ZHANG, HUI
LI, PING
YANG, ZHENG
QIN, LINGYAN
MO, WUNING
author_sort CHEN, XU
collection PubMed
description The aim of the present study was to analyze the expression of WW-domain oxidoreductase (WWOX), fragile histidine triad (FHIT) and p73 in acute lymphoblastic leukemia (ALL). Samples from 122 ALL patients and 35 non-ALL control patients were collected in this study. RT-PCR was performed to detect the mRNA expression of WWOX, FHIT and p73. The methylation status of the WWOX promoter region, FHIT promoter region and the first exon region of p73 were also analyzed using the methylation-specific PCR method. The mRNA expression of WWOX, FHIT and p73 was significantly lower in the ALL samples compared with the controls (48.2, 42.9 and 55.4%, respectively). By contrast, the methylation frequency of WWOX, FHIT and p73 was significantly higher in the ALL samples compared with the controls (44.6, 46.4 and 37.5%, respectively). The mRNA expression of these three genes was inversely correlated with the methylation frequency in the ALL samples (correlation coefficients, −0.661, −0.685 and −0.536 for WWOX, FHIT and p73, respectively). Moreover, the mRNA expression of WWOX was positively correlated with that of FHIT and p73 (correlation coefficients, 0.569 and 0.556, respectively). However, the methylation status of WWOX had no correlation with that of FHIT or p73. It was concluded that the high methylation status of WWOX, FHIT and p73 may lead to the inactivation of expression and the silencing of these genes, promoting the occurrence and development of ALL. The determination of the mRNA expression and methylation status of WWOX, FHIT and p73 may aid in the development of treatment approaches for ALL.
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spelling pubmed-37964192013-10-17 Gene expression of WWOX, FHIT and p73 in acute lymphoblastic leukemia CHEN, XU ZHANG, HUI LI, PING YANG, ZHENG QIN, LINGYAN MO, WUNING Oncol Lett Articles The aim of the present study was to analyze the expression of WW-domain oxidoreductase (WWOX), fragile histidine triad (FHIT) and p73 in acute lymphoblastic leukemia (ALL). Samples from 122 ALL patients and 35 non-ALL control patients were collected in this study. RT-PCR was performed to detect the mRNA expression of WWOX, FHIT and p73. The methylation status of the WWOX promoter region, FHIT promoter region and the first exon region of p73 were also analyzed using the methylation-specific PCR method. The mRNA expression of WWOX, FHIT and p73 was significantly lower in the ALL samples compared with the controls (48.2, 42.9 and 55.4%, respectively). By contrast, the methylation frequency of WWOX, FHIT and p73 was significantly higher in the ALL samples compared with the controls (44.6, 46.4 and 37.5%, respectively). The mRNA expression of these three genes was inversely correlated with the methylation frequency in the ALL samples (correlation coefficients, −0.661, −0.685 and −0.536 for WWOX, FHIT and p73, respectively). Moreover, the mRNA expression of WWOX was positively correlated with that of FHIT and p73 (correlation coefficients, 0.569 and 0.556, respectively). However, the methylation status of WWOX had no correlation with that of FHIT or p73. It was concluded that the high methylation status of WWOX, FHIT and p73 may lead to the inactivation of expression and the silencing of these genes, promoting the occurrence and development of ALL. The determination of the mRNA expression and methylation status of WWOX, FHIT and p73 may aid in the development of treatment approaches for ALL. D.A. Spandidos 2013-10 2013-08-05 /pmc/articles/PMC3796419/ /pubmed/24137446 http://dx.doi.org/10.3892/ol.2013.1514 Text en Copyright © 2013, 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
CHEN, XU
ZHANG, HUI
LI, PING
YANG, ZHENG
QIN, LINGYAN
MO, WUNING
Gene expression of WWOX, FHIT and p73 in acute lymphoblastic leukemia
title Gene expression of WWOX, FHIT and p73 in acute lymphoblastic leukemia
title_full Gene expression of WWOX, FHIT and p73 in acute lymphoblastic leukemia
title_fullStr Gene expression of WWOX, FHIT and p73 in acute lymphoblastic leukemia
title_full_unstemmed Gene expression of WWOX, FHIT and p73 in acute lymphoblastic leukemia
title_short Gene expression of WWOX, FHIT and p73 in acute lymphoblastic leukemia
title_sort gene expression of wwox, fhit and p73 in acute lymphoblastic leukemia
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3796419/
https://www.ncbi.nlm.nih.gov/pubmed/24137446
http://dx.doi.org/10.3892/ol.2013.1514
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