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Serological Evaluation of Soluble CD44 in Renal Cancer
In this study, we examined the feasibility of using elevated serum CD44 concentration as an indicator in renal cancer. We performed enzyme‐linked immunosorbent assays using 63 sera obtained from 47 patients with renal cancer and 16 healthy controls and evaluated the clinico‐pathological parameters....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1996
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921015/ https://www.ncbi.nlm.nih.gov/pubmed/9045950 http://dx.doi.org/10.1111/j.1349-7006.1996.tb03131.x |
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author | Kan, Masaharu Kanayama, Hiro‐omi Naruo, Seiichi Tsuji, Masahito Kojima, Keiji Kurokawa, Yasushi Kagawa, Susumu |
author_facet | Kan, Masaharu Kanayama, Hiro‐omi Naruo, Seiichi Tsuji, Masahito Kojima, Keiji Kurokawa, Yasushi Kagawa, Susumu |
author_sort | Kan, Masaharu |
collection | PubMed |
description | In this study, we examined the feasibility of using elevated serum CD44 concentration as an indicator in renal cancer. We performed enzyme‐linked immunosorbent assays using 63 sera obtained from 47 patients with renal cancer and 16 healthy controls and evaluated the clinico‐pathological parameters. The concentration of soluble CD44 standard (sCD44std), indicating the concentration of all circulating CD44 isoforms, was significantly higher in renal cancer patients than in normal individuals (745±170 ng/ml vs. 563±159 ng/ml, P=0.001). The concentration of soluble CD44 splice isoforms sharing exon v6 (sCD44v6) was also higher in the same patients (287±121 vs. 220±59, P=0.056). However, there were no correlations between the concentrations of sCD44std or sCD44v6 and clinico‐pathological parameters such as grade, stage, histological type, tumor size and growth type. The ratio of sCD44std/sCD44v6 was higher in the rapid growth‐type cancers than in the slow growth‐type cancers (3.95±2.12 vs. 2.63±0.82, P=0.014). These findings suggested that the serum concentration of unknown soluble CD44 isoforms not sharing exon v6, which are present in sCD44std, increases in patients with rapid growth‐type cancers. These findings indicated that sCD44std and sCD44v6 are not useful indicators of tumor burden and metastasis in patients with renal cancer, but that an unknown sCD44 isoform(s) plays a role in the biological behavior of the rapid growth‐type cancers. |
format | Online Article Text |
id | pubmed-5921015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59210152018-05-11 Serological Evaluation of Soluble CD44 in Renal Cancer Kan, Masaharu Kanayama, Hiro‐omi Naruo, Seiichi Tsuji, Masahito Kojima, Keiji Kurokawa, Yasushi Kagawa, Susumu Jpn J Cancer Res Article In this study, we examined the feasibility of using elevated serum CD44 concentration as an indicator in renal cancer. We performed enzyme‐linked immunosorbent assays using 63 sera obtained from 47 patients with renal cancer and 16 healthy controls and evaluated the clinico‐pathological parameters. The concentration of soluble CD44 standard (sCD44std), indicating the concentration of all circulating CD44 isoforms, was significantly higher in renal cancer patients than in normal individuals (745±170 ng/ml vs. 563±159 ng/ml, P=0.001). The concentration of soluble CD44 splice isoforms sharing exon v6 (sCD44v6) was also higher in the same patients (287±121 vs. 220±59, P=0.056). However, there were no correlations between the concentrations of sCD44std or sCD44v6 and clinico‐pathological parameters such as grade, stage, histological type, tumor size and growth type. The ratio of sCD44std/sCD44v6 was higher in the rapid growth‐type cancers than in the slow growth‐type cancers (3.95±2.12 vs. 2.63±0.82, P=0.014). These findings suggested that the serum concentration of unknown soluble CD44 isoforms not sharing exon v6, which are present in sCD44std, increases in patients with rapid growth‐type cancers. These findings indicated that sCD44std and sCD44v6 are not useful indicators of tumor burden and metastasis in patients with renal cancer, but that an unknown sCD44 isoform(s) plays a role in the biological behavior of the rapid growth‐type cancers. Blackwell Publishing Ltd 1996-11 /pmc/articles/PMC5921015/ /pubmed/9045950 http://dx.doi.org/10.1111/j.1349-7006.1996.tb03131.x Text en |
spellingShingle | Article Kan, Masaharu Kanayama, Hiro‐omi Naruo, Seiichi Tsuji, Masahito Kojima, Keiji Kurokawa, Yasushi Kagawa, Susumu Serological Evaluation of Soluble CD44 in Renal Cancer |
title | Serological Evaluation of Soluble CD44 in Renal Cancer |
title_full | Serological Evaluation of Soluble CD44 in Renal Cancer |
title_fullStr | Serological Evaluation of Soluble CD44 in Renal Cancer |
title_full_unstemmed | Serological Evaluation of Soluble CD44 in Renal Cancer |
title_short | Serological Evaluation of Soluble CD44 in Renal Cancer |
title_sort | serological evaluation of soluble cd44 in renal cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921015/ https://www.ncbi.nlm.nih.gov/pubmed/9045950 http://dx.doi.org/10.1111/j.1349-7006.1996.tb03131.x |
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