Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1782333697427505152 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4156233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT fengyan expressionofdnatopoisomeraseiiaclinicalsignificanceinlaryngealcarcinoma AT zhanghaili expressionofdnatopoisomeraseiiaclinicalsignificanceinlaryngealcarcinoma AT gaowei expressionofdnatopoisomeraseiiaclinicalsignificanceinlaryngealcarcinoma AT wenshuxin expressionofdnatopoisomeraseiiaclinicalsignificanceinlaryngealcarcinoma AT huangfuhui expressionofdnatopoisomeraseiiaclinicalsignificanceinlaryngealcarcinoma AT sunruifang expressionofdnatopoisomeraseiiaclinicalsignificanceinlaryngealcarcinoma AT baiwei expressionofdnatopoisomeraseiiaclinicalsignificanceinlaryngealcarcinoma AT wangbinquan expressionofdnatopoisomeraseiiaclinicalsignificanceinlaryngealcarcinoma |