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Expression of serum amyloid A in uterine cervical cancer
BACKGROUND: As an acute-phase protein, serum amyloid A (SAA) is expressed primarily in the liver. However, its expression in extrahepatic tissues, especially in tumor tissues, was also demonstrated recently. In our study, we investigated the expression of SAA in uterine cervical carcinomas, and our...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907664/ https://www.ncbi.nlm.nih.gov/pubmed/24447576 http://dx.doi.org/10.1186/1746-1596-9-16 |
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author | Ren, Yanjie Wang, He Lu, Donghao Xie, Xiaoyan Chen, Xinlian Peng, Jing Hu, Qian Shi, Gang Liu, Shanling |
author_facet | Ren, Yanjie Wang, He Lu, Donghao Xie, Xiaoyan Chen, Xinlian Peng, Jing Hu, Qian Shi, Gang Liu, Shanling |
author_sort | Ren, Yanjie |
collection | PubMed |
description | BACKGROUND: As an acute-phase protein, serum amyloid A (SAA) is expressed primarily in the liver. However, its expression in extrahepatic tissues, especially in tumor tissues, was also demonstrated recently. In our study, we investigated the expression of SAA in uterine cervical carcinomas, and our results suggested its potential as a serum biomarker. METHODS: Quantitative real-time polymerase chain reaction (RT-PCR), immunohistochemistry (IHC) and enzyme-linked immunosorbent assay (ELISA) were used to evaluate the SAA gene and protein expression levels in the tissues and sera of patients with non-neoplastic lesions (NNLs), cervical intraepithelial neoplasia (CIN) and cervical carcinoma (CC). RESULTS: Compared with NNLs, the SAA gene (SAA1 and SAA4) expression levels were significantly higher in uterine CC (mean copy numbers: 138.7 vs. 5.01, P < 0.000; and 1.8 vs. 0.079, P = 0.001, respectively) by real-time PCR. IHC revealed cytoplasmic SAA protein staining in tissues from adenocarcinoma and squamous cell carcinoma of the cervix. The median serum concentrations (μg/ml) of SAA were 6.02 in patients with NNLs and 10.98 in patients with CIN (P = 0.31). In contrast, the median serum SAA concentration was 23.7 μg/ml in uterine CC patients, which was significantly higher than the SAA concentrations of the NNL group (P = 0.002) and the CIN group (P = 0.024). CONCLUSIONS: Our data suggested that SAA might be a uterine CC cell product. High SAA concentrations in the serum of CC patients may have a role in monitoring disease occurrence and could have therapeutic applications. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1433263219102962. |
format | Online Article Text |
id | pubmed-3907664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39076642014-02-01 Expression of serum amyloid A in uterine cervical cancer Ren, Yanjie Wang, He Lu, Donghao Xie, Xiaoyan Chen, Xinlian Peng, Jing Hu, Qian Shi, Gang Liu, Shanling Diagn Pathol Research BACKGROUND: As an acute-phase protein, serum amyloid A (SAA) is expressed primarily in the liver. However, its expression in extrahepatic tissues, especially in tumor tissues, was also demonstrated recently. In our study, we investigated the expression of SAA in uterine cervical carcinomas, and our results suggested its potential as a serum biomarker. METHODS: Quantitative real-time polymerase chain reaction (RT-PCR), immunohistochemistry (IHC) and enzyme-linked immunosorbent assay (ELISA) were used to evaluate the SAA gene and protein expression levels in the tissues and sera of patients with non-neoplastic lesions (NNLs), cervical intraepithelial neoplasia (CIN) and cervical carcinoma (CC). RESULTS: Compared with NNLs, the SAA gene (SAA1 and SAA4) expression levels were significantly higher in uterine CC (mean copy numbers: 138.7 vs. 5.01, P < 0.000; and 1.8 vs. 0.079, P = 0.001, respectively) by real-time PCR. IHC revealed cytoplasmic SAA protein staining in tissues from adenocarcinoma and squamous cell carcinoma of the cervix. The median serum concentrations (μg/ml) of SAA were 6.02 in patients with NNLs and 10.98 in patients with CIN (P = 0.31). In contrast, the median serum SAA concentration was 23.7 μg/ml in uterine CC patients, which was significantly higher than the SAA concentrations of the NNL group (P = 0.002) and the CIN group (P = 0.024). CONCLUSIONS: Our data suggested that SAA might be a uterine CC cell product. High SAA concentrations in the serum of CC patients may have a role in monitoring disease occurrence and could have therapeutic applications. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1433263219102962. BioMed Central 2014-01-21 /pmc/articles/PMC3907664/ /pubmed/24447576 http://dx.doi.org/10.1186/1746-1596-9-16 Text en Copyright © 2014 Ren et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Ren, Yanjie Wang, He Lu, Donghao Xie, Xiaoyan Chen, Xinlian Peng, Jing Hu, Qian Shi, Gang Liu, Shanling Expression of serum amyloid A in uterine cervical cancer |
title | Expression of serum amyloid A in uterine cervical cancer |
title_full | Expression of serum amyloid A in uterine cervical cancer |
title_fullStr | Expression of serum amyloid A in uterine cervical cancer |
title_full_unstemmed | Expression of serum amyloid A in uterine cervical cancer |
title_short | Expression of serum amyloid A in uterine cervical cancer |
title_sort | expression of serum amyloid a in uterine cervical cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907664/ https://www.ncbi.nlm.nih.gov/pubmed/24447576 http://dx.doi.org/10.1186/1746-1596-9-16 |
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