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Expression of CIDE proteins in clear cell renal cell carcinoma and their prognostic significance
Clear cell renal cell carcinoma (ccRCC) is the major and aggressive subtype of renal cell carcinoma. It is known to derive its histologic appearance from accumulation of abundant lipids and glycogens. The cell death-inducing DFF45-like effector (CIDE) family has been characterized as the lipid dropl...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634988/ https://www.ncbi.nlm.nih.gov/pubmed/23475172 http://dx.doi.org/10.1007/s11010-013-1605-y |
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author | Yu, Ming Wang, Hui Zhao, Jun Yuan, Yuan Wang, Chao Li, Jing Zhang, Lijun Zhang, Liying Li, Qing Ye, Jing |
author_facet | Yu, Ming Wang, Hui Zhao, Jun Yuan, Yuan Wang, Chao Li, Jing Zhang, Lijun Zhang, Liying Li, Qing Ye, Jing |
author_sort | Yu, Ming |
collection | PubMed |
description | Clear cell renal cell carcinoma (ccRCC) is the major and aggressive subtype of renal cell carcinoma. It is known to derive its histologic appearance from accumulation of abundant lipids and glycogens. The cell death-inducing DFF45-like effector (CIDE) family has been characterized as the lipid droplet proteins involved in the metabolism of lipid storage droplets. The purpose of this study was to evaluate the expression of CIDE proteins in ccRCC cells and to investigate their prognostic significance. We examined consecutive patients with sporadic ccRCC, who underwent nephrectomy, to measure their mRNA and protein expression of CIDE proteins. We found that Cidec and ADRP expression were significantly up-regulated in ccRCC, compared with normal kidney tissues. Cideb was down-regulated. We also found that Cideb was expressed more in low-grade ccRCC than in high-grade tumors. To further clarify the relationship between Cideb expression and patient prognosis, we evaluated 57 ccRCC patients followed up for 120 months. Reduced ccRCC Cideb expression was associated with a higher Fuhrman nuclear grade. Patients with high Cideb expression had better overall survival rate than those with low expression (p < 0.05). Cideb expression was an independent predictor of survival (p = 0.001). Although the biologic function of Cideb in ccRCC remains unknown, the expression level of Cideb might be a novel predictor of prognosis in ccRCC. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11010-013-1605-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3634988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-36349882013-04-26 Expression of CIDE proteins in clear cell renal cell carcinoma and their prognostic significance Yu, Ming Wang, Hui Zhao, Jun Yuan, Yuan Wang, Chao Li, Jing Zhang, Lijun Zhang, Liying Li, Qing Ye, Jing Mol Cell Biochem Article Clear cell renal cell carcinoma (ccRCC) is the major and aggressive subtype of renal cell carcinoma. It is known to derive its histologic appearance from accumulation of abundant lipids and glycogens. The cell death-inducing DFF45-like effector (CIDE) family has been characterized as the lipid droplet proteins involved in the metabolism of lipid storage droplets. The purpose of this study was to evaluate the expression of CIDE proteins in ccRCC cells and to investigate their prognostic significance. We examined consecutive patients with sporadic ccRCC, who underwent nephrectomy, to measure their mRNA and protein expression of CIDE proteins. We found that Cidec and ADRP expression were significantly up-regulated in ccRCC, compared with normal kidney tissues. Cideb was down-regulated. We also found that Cideb was expressed more in low-grade ccRCC than in high-grade tumors. To further clarify the relationship between Cideb expression and patient prognosis, we evaluated 57 ccRCC patients followed up for 120 months. Reduced ccRCC Cideb expression was associated with a higher Fuhrman nuclear grade. Patients with high Cideb expression had better overall survival rate than those with low expression (p < 0.05). Cideb expression was an independent predictor of survival (p = 0.001). Although the biologic function of Cideb in ccRCC remains unknown, the expression level of Cideb might be a novel predictor of prognosis in ccRCC. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11010-013-1605-y) contains supplementary material, which is available to authorized users. Springer US 2013-03-11 2013 /pmc/articles/PMC3634988/ /pubmed/23475172 http://dx.doi.org/10.1007/s11010-013-1605-y Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Article Yu, Ming Wang, Hui Zhao, Jun Yuan, Yuan Wang, Chao Li, Jing Zhang, Lijun Zhang, Liying Li, Qing Ye, Jing Expression of CIDE proteins in clear cell renal cell carcinoma and their prognostic significance |
title | Expression of CIDE proteins in clear cell renal cell carcinoma and their prognostic significance |
title_full | Expression of CIDE proteins in clear cell renal cell carcinoma and their prognostic significance |
title_fullStr | Expression of CIDE proteins in clear cell renal cell carcinoma and their prognostic significance |
title_full_unstemmed | Expression of CIDE proteins in clear cell renal cell carcinoma and their prognostic significance |
title_short | Expression of CIDE proteins in clear cell renal cell carcinoma and their prognostic significance |
title_sort | expression of cide proteins in clear cell renal cell carcinoma and their prognostic significance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634988/ https://www.ncbi.nlm.nih.gov/pubmed/23475172 http://dx.doi.org/10.1007/s11010-013-1605-y |
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