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Clinicopathologic significance of CXCR4 and Nrf2 in colorectal cancer
The CXCR4 and Nrf2 signaling pathways are abnormally activated in response to cellular stress in various types of human cancers. In this study, we examined the expression of CXCR4 and Nrf2 in colorectal cancer (CRC) tissue specimens and investigated their correlation with patient clinicopathologic c...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Editorial Department of Journal of Biomedical Research
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721036/ https://www.ncbi.nlm.nih.gov/pubmed/23885267 http://dx.doi.org/10.7555/JBR.27.20130069 |
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author | Hu, Tinghua Yao, Yu Yu, Shuo Guo, Hui Han, Lili Wang, Wenjuan Tian, Tao Hao, Yibin Liu, Zhiyan Nan, Kejun Wang, Shuhong |
author_facet | Hu, Tinghua Yao, Yu Yu, Shuo Guo, Hui Han, Lili Wang, Wenjuan Tian, Tao Hao, Yibin Liu, Zhiyan Nan, Kejun Wang, Shuhong |
author_sort | Hu, Tinghua |
collection | PubMed |
description | The CXCR4 and Nrf2 signaling pathways are abnormally activated in response to cellular stress in various types of human cancers. In this study, we examined the expression of CXCR4 and Nrf2 in colorectal cancer (CRC) tissue specimens and investigated their correlation with patient clinicopathologic characteristics. We determined CXCR4 and Nrf2 expression in 76 CRC tissue specimens and paired normal tissue specimens by immunohistochemistry and real-time PCR. We found that the protein and mRNA transcript levels of CXCR4 were significantly higher in CRC tissue specimens than in paired normal tissues, while the expressions of Nrf2 protein and mRNA were increased in CRC tissues compared to distant non-cancerous tissues. High expression level of CXCR4 was positively correlated with poorly differentiated (P = 0.031), more advanced tumor-node-metastasis (TNM) stage (P = 0.019), lymph node metastasis (P = 0.007) and distant metastasis (P = 0.018). However, the expression of Nrf2 protein was positively correlated with larger tumor size (P = 0.049), more advanced TNM stage (P = 0.013), lymph node metastasis (P = 0.016) and distant metastasis (P = 0.023). Moreover, there was a strong relationship between CXCR4 and Nrf2 expression in CRC tissues, indicating that high Nrf2 expression may contribute to CXCR4 overexpression. In addition, combined expression of CXCR4 and Nrf2 strongly correlated with lymph node metastasis and distant metastasis (P = 0.003). Furthermore, we found that combined high expression of CXCR4 and Nrf2 had stronger correlation with lymph node metastasis and distant metastasis than any single molecule did. This study indicated that the abnormal expression of CXCR4 and Nrf2 contributed to the progression of CRC. |
format | Online Article Text |
id | pubmed-3721036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Editorial Department of Journal of Biomedical Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-37210362013-07-24 Clinicopathologic significance of CXCR4 and Nrf2 in colorectal cancer Hu, Tinghua Yao, Yu Yu, Shuo Guo, Hui Han, Lili Wang, Wenjuan Tian, Tao Hao, Yibin Liu, Zhiyan Nan, Kejun Wang, Shuhong J Biomed Res Research Paper The CXCR4 and Nrf2 signaling pathways are abnormally activated in response to cellular stress in various types of human cancers. In this study, we examined the expression of CXCR4 and Nrf2 in colorectal cancer (CRC) tissue specimens and investigated their correlation with patient clinicopathologic characteristics. We determined CXCR4 and Nrf2 expression in 76 CRC tissue specimens and paired normal tissue specimens by immunohistochemistry and real-time PCR. We found that the protein and mRNA transcript levels of CXCR4 were significantly higher in CRC tissue specimens than in paired normal tissues, while the expressions of Nrf2 protein and mRNA were increased in CRC tissues compared to distant non-cancerous tissues. High expression level of CXCR4 was positively correlated with poorly differentiated (P = 0.031), more advanced tumor-node-metastasis (TNM) stage (P = 0.019), lymph node metastasis (P = 0.007) and distant metastasis (P = 0.018). However, the expression of Nrf2 protein was positively correlated with larger tumor size (P = 0.049), more advanced TNM stage (P = 0.013), lymph node metastasis (P = 0.016) and distant metastasis (P = 0.023). Moreover, there was a strong relationship between CXCR4 and Nrf2 expression in CRC tissues, indicating that high Nrf2 expression may contribute to CXCR4 overexpression. In addition, combined expression of CXCR4 and Nrf2 strongly correlated with lymph node metastasis and distant metastasis (P = 0.003). Furthermore, we found that combined high expression of CXCR4 and Nrf2 had stronger correlation with lymph node metastasis and distant metastasis than any single molecule did. This study indicated that the abnormal expression of CXCR4 and Nrf2 contributed to the progression of CRC. Editorial Department of Journal of Biomedical Research 2013-07 2013-07-06 /pmc/articles/PMC3721036/ /pubmed/23885267 http://dx.doi.org/10.7555/JBR.27.20130069 Text en © 2013 by the Journal of Biomedical Research. All rights reserved. |
spellingShingle | Research Paper Hu, Tinghua Yao, Yu Yu, Shuo Guo, Hui Han, Lili Wang, Wenjuan Tian, Tao Hao, Yibin Liu, Zhiyan Nan, Kejun Wang, Shuhong Clinicopathologic significance of CXCR4 and Nrf2 in colorectal cancer |
title | Clinicopathologic significance of CXCR4 and Nrf2 in colorectal cancer |
title_full | Clinicopathologic significance of CXCR4 and Nrf2 in colorectal cancer |
title_fullStr | Clinicopathologic significance of CXCR4 and Nrf2 in colorectal cancer |
title_full_unstemmed | Clinicopathologic significance of CXCR4 and Nrf2 in colorectal cancer |
title_short | Clinicopathologic significance of CXCR4 and Nrf2 in colorectal cancer |
title_sort | clinicopathologic significance of cxcr4 and nrf2 in colorectal cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721036/ https://www.ncbi.nlm.nih.gov/pubmed/23885267 http://dx.doi.org/10.7555/JBR.27.20130069 |
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