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The Vitamin D status is associated with serum C-reactive protein and adhesion molecules in patients with renal cell carcinoma

Low vitamin D status is associated with an increased risk of renal cell carcinoma (RCC). This study investigated the association of vitamin D status with serum C-reactive protein (CRP) and adhesion molecules among RCC patients. Fifty newly diagnosed RCC patients and 100 age- and sex-matched controls...

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Autores principales: Xu, Shen, Song, Jin, Zhang, Zhi-Hui, Fu, Lin, Gao, Lan, Xie, Dong-Dong, Yu, De-Xin, Xu, De-Xiang, Sun, Guo-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853912/
https://www.ncbi.nlm.nih.gov/pubmed/31723229
http://dx.doi.org/10.1038/s41598-019-53395-9
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author Xu, Shen
Song, Jin
Zhang, Zhi-Hui
Fu, Lin
Gao, Lan
Xie, Dong-Dong
Yu, De-Xin
Xu, De-Xiang
Sun, Guo-Ping
author_facet Xu, Shen
Song, Jin
Zhang, Zhi-Hui
Fu, Lin
Gao, Lan
Xie, Dong-Dong
Yu, De-Xin
Xu, De-Xiang
Sun, Guo-Ping
author_sort Xu, Shen
collection PubMed
description Low vitamin D status is associated with an increased risk of renal cell carcinoma (RCC). This study investigated the association of vitamin D status with serum C-reactive protein (CRP) and adhesion molecules among RCC patients. Fifty newly diagnosed RCC patients and 100 age- and sex-matched controls were recruited. As expected, serum 25(OH)D level was lower in RCC patients than in controls. By contrast, serum levels of CRP, an inflammatory molecule, and ICAM, LAMA4 and EpCAM, three adhesion molecules, were higher in RCC patients than in controls. All RCC patients were divided into two groups: H-VitD (>20 ng/ml) or L-VitD (<20 ng/ml). Interestingly, the levels of serum CRP and all adhesion molecules were higher in RCC patients with L-VitD than those with H-VitD. Nuclear vitamin D receptor (VDR) was downregulated and nuclear factor kappa B (NF-κB) was activated in cancerous tissues. The in vitro experiments found that VitD3 suppressed NF-κB activation and adhesion molecules in RCC cells. Moreover, VitD3 suppressed NF-κB through reinforcing physical interaction between VDR and NF-κB p65 subunit in RCC cells. These results provide a mechanistic explanation for the association among low vitamin D status, local inflammation and increased expression of adhesion molecules among RCC patients.
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spelling pubmed-68539122019-11-19 The Vitamin D status is associated with serum C-reactive protein and adhesion molecules in patients with renal cell carcinoma Xu, Shen Song, Jin Zhang, Zhi-Hui Fu, Lin Gao, Lan Xie, Dong-Dong Yu, De-Xin Xu, De-Xiang Sun, Guo-Ping Sci Rep Article Low vitamin D status is associated with an increased risk of renal cell carcinoma (RCC). This study investigated the association of vitamin D status with serum C-reactive protein (CRP) and adhesion molecules among RCC patients. Fifty newly diagnosed RCC patients and 100 age- and sex-matched controls were recruited. As expected, serum 25(OH)D level was lower in RCC patients than in controls. By contrast, serum levels of CRP, an inflammatory molecule, and ICAM, LAMA4 and EpCAM, three adhesion molecules, were higher in RCC patients than in controls. All RCC patients were divided into two groups: H-VitD (>20 ng/ml) or L-VitD (<20 ng/ml). Interestingly, the levels of serum CRP and all adhesion molecules were higher in RCC patients with L-VitD than those with H-VitD. Nuclear vitamin D receptor (VDR) was downregulated and nuclear factor kappa B (NF-κB) was activated in cancerous tissues. The in vitro experiments found that VitD3 suppressed NF-κB activation and adhesion molecules in RCC cells. Moreover, VitD3 suppressed NF-κB through reinforcing physical interaction between VDR and NF-κB p65 subunit in RCC cells. These results provide a mechanistic explanation for the association among low vitamin D status, local inflammation and increased expression of adhesion molecules among RCC patients. Nature Publishing Group UK 2019-11-13 /pmc/articles/PMC6853912/ /pubmed/31723229 http://dx.doi.org/10.1038/s41598-019-53395-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Xu, Shen
Song, Jin
Zhang, Zhi-Hui
Fu, Lin
Gao, Lan
Xie, Dong-Dong
Yu, De-Xin
Xu, De-Xiang
Sun, Guo-Ping
The Vitamin D status is associated with serum C-reactive protein and adhesion molecules in patients with renal cell carcinoma
title The Vitamin D status is associated with serum C-reactive protein and adhesion molecules in patients with renal cell carcinoma
title_full The Vitamin D status is associated with serum C-reactive protein and adhesion molecules in patients with renal cell carcinoma
title_fullStr The Vitamin D status is associated with serum C-reactive protein and adhesion molecules in patients with renal cell carcinoma
title_full_unstemmed The Vitamin D status is associated with serum C-reactive protein and adhesion molecules in patients with renal cell carcinoma
title_short The Vitamin D status is associated with serum C-reactive protein and adhesion molecules in patients with renal cell carcinoma
title_sort vitamin d status is associated with serum c-reactive protein and adhesion molecules in patients with renal cell carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853912/
https://www.ncbi.nlm.nih.gov/pubmed/31723229
http://dx.doi.org/10.1038/s41598-019-53395-9
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