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Expression of DNA topoisomerase II-α: Clinical significance in laryngeal carcinoma

DNA topoisomerase II-α (Topo II-α) is essential for numerous cell processes, including DNA replication, transcription, recombination, and chromosome separation and condensation. Altered Topo II-α expression may lead to carcinogenesis and cancer progression. The aim of the present study was to invest...

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Autores principales: FENG, YAN, ZHANG, HAILI, GAO, WEI, WEN, SHUXIN, HUANGFU, HUI, SUN, RUIFANG, BAI, WEI, WANG, BINQUAN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156233/
https://www.ncbi.nlm.nih.gov/pubmed/25202370
http://dx.doi.org/10.3892/ol.2014.2367
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author FENG, YAN
ZHANG, HAILI
GAO, WEI
WEN, SHUXIN
HUANGFU, HUI
SUN, RUIFANG
BAI, WEI
WANG, BINQUAN
author_facet FENG, YAN
ZHANG, HAILI
GAO, WEI
WEN, SHUXIN
HUANGFU, HUI
SUN, RUIFANG
BAI, WEI
WANG, BINQUAN
author_sort FENG, YAN
collection PubMed
description DNA topoisomerase II-α (Topo II-α) is essential for numerous cell processes, including DNA replication, transcription, recombination, and chromosome separation and condensation. Altered Topo II-α expression may lead to carcinogenesis and cancer progression. The aim of the present study was to investigate the association between Topo II-α expression levels and clinicopathological data from laryngeal cancer patients. Immunohistochemistry was used to analyze Topo II-α expression in laryngeal squamous cell carcinoma and distant healthy tissues obtained from 70 patients. In addition, fluorescence in situ hybridization was used to detect Topo II-α amplification and chromosome 17 ploidy using a laryngeal cancer tissue microarray. The expression of Topo II-α protein was detected in 71.43% (50/70) of laryngeal carcinoma tissues, in contrast to 9% of healthy tissues (2/22). Furthermore, the expression of Topo II-α protein was found to be associated with tumor de-differentiation and advanced tumor T stage. However, the expression of Topo II-α protein was not identified to be associated with Topo II-α amplification in laryngeal carcinoma, although was found to positively correlate with chromosome 17 aneuploidy (P<0.05). A higher aneuploidy rate contributed to increased expression levels of Topo II-α protein. Aberrant Topo II-α expression and chromosome 17 aneuploidy contributed to the development and progression of laryngeal cancer, indicating that targeting Topo II-α may provide a treatment strategy for patients with laryngeal cancer.
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spelling pubmed-41562332014-09-08 Expression of DNA topoisomerase II-α: Clinical significance in laryngeal carcinoma FENG, YAN ZHANG, HAILI GAO, WEI WEN, SHUXIN HUANGFU, HUI SUN, RUIFANG BAI, WEI WANG, BINQUAN Oncol Lett Articles DNA topoisomerase II-α (Topo II-α) is essential for numerous cell processes, including DNA replication, transcription, recombination, and chromosome separation and condensation. Altered Topo II-α expression may lead to carcinogenesis and cancer progression. The aim of the present study was to investigate the association between Topo II-α expression levels and clinicopathological data from laryngeal cancer patients. Immunohistochemistry was used to analyze Topo II-α expression in laryngeal squamous cell carcinoma and distant healthy tissues obtained from 70 patients. In addition, fluorescence in situ hybridization was used to detect Topo II-α amplification and chromosome 17 ploidy using a laryngeal cancer tissue microarray. The expression of Topo II-α protein was detected in 71.43% (50/70) of laryngeal carcinoma tissues, in contrast to 9% of healthy tissues (2/22). Furthermore, the expression of Topo II-α protein was found to be associated with tumor de-differentiation and advanced tumor T stage. However, the expression of Topo II-α protein was not identified to be associated with Topo II-α amplification in laryngeal carcinoma, although was found to positively correlate with chromosome 17 aneuploidy (P<0.05). A higher aneuploidy rate contributed to increased expression levels of Topo II-α protein. Aberrant Topo II-α expression and chromosome 17 aneuploidy contributed to the development and progression of laryngeal cancer, indicating that targeting Topo II-α may provide a treatment strategy for patients with laryngeal cancer. D.A. Spandidos 2014-10 2014-07-22 /pmc/articles/PMC4156233/ /pubmed/25202370 http://dx.doi.org/10.3892/ol.2014.2367 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
FENG, YAN
ZHANG, HAILI
GAO, WEI
WEN, SHUXIN
HUANGFU, HUI
SUN, RUIFANG
BAI, WEI
WANG, BINQUAN
Expression of DNA topoisomerase II-α: Clinical significance in laryngeal carcinoma
title Expression of DNA topoisomerase II-α: Clinical significance in laryngeal carcinoma
title_full Expression of DNA topoisomerase II-α: Clinical significance in laryngeal carcinoma
title_fullStr Expression of DNA topoisomerase II-α: Clinical significance in laryngeal carcinoma
title_full_unstemmed Expression of DNA topoisomerase II-α: Clinical significance in laryngeal carcinoma
title_short Expression of DNA topoisomerase II-α: Clinical significance in laryngeal carcinoma
title_sort expression of dna topoisomerase ii-α: clinical significance in laryngeal carcinoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156233/
https://www.ncbi.nlm.nih.gov/pubmed/25202370
http://dx.doi.org/10.3892/ol.2014.2367
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