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Expression and clinical significance of cytochrome c oxidase subunit IV in colorectal cancer patients

INTRODUCTION: Previous studies have demonstrated that the expression of cytochrome c oxidase (COX) subunits encoded by mitochondrial DNA is elevated in colorectal cancer (CRC). However, the expression of nuclear DNA-encoded COX IV and its clinical significance have not yet been investigated in CRC....

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Autores principales: Zhang, Kun, Chen, Yibing, Huang, Xiaojun, Qu, Ping, Pan, Qiuzhong, Lü, Lin, Jiang, Shanshan, Ren, Tingitng, Su, Haichuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754367/
https://www.ncbi.nlm.nih.gov/pubmed/26925120
http://dx.doi.org/10.5114/aoms.2016.57581
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author Zhang, Kun
Chen, Yibing
Huang, Xiaojun
Qu, Ping
Pan, Qiuzhong
Lü, Lin
Jiang, Shanshan
Ren, Tingitng
Su, Haichuan
author_facet Zhang, Kun
Chen, Yibing
Huang, Xiaojun
Qu, Ping
Pan, Qiuzhong
Lü, Lin
Jiang, Shanshan
Ren, Tingitng
Su, Haichuan
author_sort Zhang, Kun
collection PubMed
description INTRODUCTION: Previous studies have demonstrated that the expression of cytochrome c oxidase (COX) subunits encoded by mitochondrial DNA is elevated in colorectal cancer (CRC). However, the expression of nuclear DNA-encoded COX IV and its clinical significance have not yet been investigated in CRC. MATERIAL AND METHODS: We examined COX IV expression in paired CRC samples (cancer and pericancerous tissues) by quantitative real-time polymerase chain reaction (qPCR), Western blot and immunohistochemical staining and analyzed its clinical significance. RESULTS: qPCR and Western blot analyses showed that COX IV expression was significantly elevated at both the mRNA (p = 0.05) and protein levels in CRC tissue samples when compared with those in paired pericancerous tissues. Immunohistochemistry also revealed that COX IV expression was significantly increased in CRC tissues (p < 0.001). Association analyses showed that there was no significant association between COX IV expression and clinical parameters of CRC patients except for gender (p = 0.017). Moreover, we did not find any association between COX IV expression and overall survival or recurrence-free survival of CRC patients. Further analysis showed no significant relationship between the expression of COX IV and proliferating cell nuclear antigen (PCNA), a marker of cell proliferation. CONCLUSIONS: Our findings suggest that elevated COX IV expression may play an important role in colorectal carcinogenesis, but not in progression, which warrants further investigation in future studies.
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spelling pubmed-47543672016-02-26 Expression and clinical significance of cytochrome c oxidase subunit IV in colorectal cancer patients Zhang, Kun Chen, Yibing Huang, Xiaojun Qu, Ping Pan, Qiuzhong Lü, Lin Jiang, Shanshan Ren, Tingitng Su, Haichuan Arch Med Sci Clinical Research INTRODUCTION: Previous studies have demonstrated that the expression of cytochrome c oxidase (COX) subunits encoded by mitochondrial DNA is elevated in colorectal cancer (CRC). However, the expression of nuclear DNA-encoded COX IV and its clinical significance have not yet been investigated in CRC. MATERIAL AND METHODS: We examined COX IV expression in paired CRC samples (cancer and pericancerous tissues) by quantitative real-time polymerase chain reaction (qPCR), Western blot and immunohistochemical staining and analyzed its clinical significance. RESULTS: qPCR and Western blot analyses showed that COX IV expression was significantly elevated at both the mRNA (p = 0.05) and protein levels in CRC tissue samples when compared with those in paired pericancerous tissues. Immunohistochemistry also revealed that COX IV expression was significantly increased in CRC tissues (p < 0.001). Association analyses showed that there was no significant association between COX IV expression and clinical parameters of CRC patients except for gender (p = 0.017). Moreover, we did not find any association between COX IV expression and overall survival or recurrence-free survival of CRC patients. Further analysis showed no significant relationship between the expression of COX IV and proliferating cell nuclear antigen (PCNA), a marker of cell proliferation. CONCLUSIONS: Our findings suggest that elevated COX IV expression may play an important role in colorectal carcinogenesis, but not in progression, which warrants further investigation in future studies. Termedia Publishing House 2016-02-02 2016-02-01 /pmc/articles/PMC4754367/ /pubmed/26925120 http://dx.doi.org/10.5114/aoms.2016.57581 Text en Copyright © 2016 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Clinical Research
Zhang, Kun
Chen, Yibing
Huang, Xiaojun
Qu, Ping
Pan, Qiuzhong
Lü, Lin
Jiang, Shanshan
Ren, Tingitng
Su, Haichuan
Expression and clinical significance of cytochrome c oxidase subunit IV in colorectal cancer patients
title Expression and clinical significance of cytochrome c oxidase subunit IV in colorectal cancer patients
title_full Expression and clinical significance of cytochrome c oxidase subunit IV in colorectal cancer patients
title_fullStr Expression and clinical significance of cytochrome c oxidase subunit IV in colorectal cancer patients
title_full_unstemmed Expression and clinical significance of cytochrome c oxidase subunit IV in colorectal cancer patients
title_short Expression and clinical significance of cytochrome c oxidase subunit IV in colorectal cancer patients
title_sort expression and clinical significance of cytochrome c oxidase subunit iv in colorectal cancer patients
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754367/
https://www.ncbi.nlm.nih.gov/pubmed/26925120
http://dx.doi.org/10.5114/aoms.2016.57581
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