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Clinical Significance of Serum Soluble T Cell Regulatory Molecules in Clear Cell Renal Cell Carcinoma
To clarify the role of serum soluble T cell regulatory molecules in clear cell renal cell carcinoma (CCRCC), we measured the serum levels of soluble interleukin-2 receptor (sIL-2R), soluble B7-H3 (sB7-H3), and soluble cytotoxic T lymphocyte associated antigen-4 (sCTLA-4) in 70 CCRCC patients and 35...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4095742/ https://www.ncbi.nlm.nih.gov/pubmed/25089268 http://dx.doi.org/10.1155/2014/396064 |
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author | Masuda, Akinori Arai, Kyoko Nishihara, Daisaku Mizuno, Tomoya Yuki, Hideo Kambara, Tsunehito Betsunoh, Hironori Abe, Hideyuki Yashi, Masahiro Fukabori, Yoshitatsu Yoshida, Ken-Ichiro Kamai, Takao |
author_facet | Masuda, Akinori Arai, Kyoko Nishihara, Daisaku Mizuno, Tomoya Yuki, Hideo Kambara, Tsunehito Betsunoh, Hironori Abe, Hideyuki Yashi, Masahiro Fukabori, Yoshitatsu Yoshida, Ken-Ichiro Kamai, Takao |
author_sort | Masuda, Akinori |
collection | PubMed |
description | To clarify the role of serum soluble T cell regulatory molecules in clear cell renal cell carcinoma (CCRCC), we measured the serum levels of soluble interleukin-2 receptor (sIL-2R), soluble B7-H3 (sB7-H3), and soluble cytotoxic T lymphocyte associated antigen-4 (sCTLA-4) in 70 CCRCC patients and 35 healthy controls. We investigated correlations between the serum levels of these soluble T cell regulatory molecules and the pathological grade, clinical stage, and prognosis of CCRCC. We also assessed the relations among each of these soluble molecules. As a result, the serum level of sIL-2R was significantly higher in CCRCC patients than in healthy controls (P < 0.05). In addition, elevation of serum sIL-2R was significantly correlated with the clinical stage (P < 0.001), and the survival of patients with high sIL-2R levels was shorter than that of patients with low sIL-2R levels (P < 0.05). Furthermore, the serum level of sB7-H3 was also significantly correlated with the clinical stage (P < 0.05), while the sIL-2R and sB7-H3 levels showed a positive correlation with each other (R = 0.550, P < 0.0001). These results indicate that the serum level of sIL-2R reflects tumor progression in CCRCC patients. In addition, the possibility was suggested that the IL-2/IL-2R and B7-H3 pathways may be involved in the progression of CCRCC. |
format | Online Article Text |
id | pubmed-4095742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-40957422014-08-03 Clinical Significance of Serum Soluble T Cell Regulatory Molecules in Clear Cell Renal Cell Carcinoma Masuda, Akinori Arai, Kyoko Nishihara, Daisaku Mizuno, Tomoya Yuki, Hideo Kambara, Tsunehito Betsunoh, Hironori Abe, Hideyuki Yashi, Masahiro Fukabori, Yoshitatsu Yoshida, Ken-Ichiro Kamai, Takao Biomed Res Int Research Article To clarify the role of serum soluble T cell regulatory molecules in clear cell renal cell carcinoma (CCRCC), we measured the serum levels of soluble interleukin-2 receptor (sIL-2R), soluble B7-H3 (sB7-H3), and soluble cytotoxic T lymphocyte associated antigen-4 (sCTLA-4) in 70 CCRCC patients and 35 healthy controls. We investigated correlations between the serum levels of these soluble T cell regulatory molecules and the pathological grade, clinical stage, and prognosis of CCRCC. We also assessed the relations among each of these soluble molecules. As a result, the serum level of sIL-2R was significantly higher in CCRCC patients than in healthy controls (P < 0.05). In addition, elevation of serum sIL-2R was significantly correlated with the clinical stage (P < 0.001), and the survival of patients with high sIL-2R levels was shorter than that of patients with low sIL-2R levels (P < 0.05). Furthermore, the serum level of sB7-H3 was also significantly correlated with the clinical stage (P < 0.05), while the sIL-2R and sB7-H3 levels showed a positive correlation with each other (R = 0.550, P < 0.0001). These results indicate that the serum level of sIL-2R reflects tumor progression in CCRCC patients. In addition, the possibility was suggested that the IL-2/IL-2R and B7-H3 pathways may be involved in the progression of CCRCC. Hindawi Publishing Corporation 2014 2014-06-25 /pmc/articles/PMC4095742/ /pubmed/25089268 http://dx.doi.org/10.1155/2014/396064 Text en Copyright © 2014 Akinori Masuda et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Masuda, Akinori Arai, Kyoko Nishihara, Daisaku Mizuno, Tomoya Yuki, Hideo Kambara, Tsunehito Betsunoh, Hironori Abe, Hideyuki Yashi, Masahiro Fukabori, Yoshitatsu Yoshida, Ken-Ichiro Kamai, Takao Clinical Significance of Serum Soluble T Cell Regulatory Molecules in Clear Cell Renal Cell Carcinoma |
title | Clinical Significance of Serum Soluble T Cell Regulatory Molecules in Clear Cell Renal Cell Carcinoma |
title_full | Clinical Significance of Serum Soluble T Cell Regulatory Molecules in Clear Cell Renal Cell Carcinoma |
title_fullStr | Clinical Significance of Serum Soluble T Cell Regulatory Molecules in Clear Cell Renal Cell Carcinoma |
title_full_unstemmed | Clinical Significance of Serum Soluble T Cell Regulatory Molecules in Clear Cell Renal Cell Carcinoma |
title_short | Clinical Significance of Serum Soluble T Cell Regulatory Molecules in Clear Cell Renal Cell Carcinoma |
title_sort | clinical significance of serum soluble t cell regulatory molecules in clear cell renal cell carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4095742/ https://www.ncbi.nlm.nih.gov/pubmed/25089268 http://dx.doi.org/10.1155/2014/396064 |
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