Literature DB >> 9045950

Serological evaluation of soluble CD44 in renal cancer.

M Kan1, H Kanayama, S Naruo, M Tsuji, K Kojima, Y Kurokawa, S Kagawa.   

Abstract

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.

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Year:  1996        PMID: 9045950      PMCID: PMC5921015          DOI: 10.1111/j.1349-7006.1996.tb03131.x

Source DB:  PubMed          Journal:  Jpn J Cancer Res        ISSN: 0910-5050


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  4 in total

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3.  Blood classical monocytes phenotype is not altered in primary non-small cell lung cancer.

Authors:  Saleh A Almatroodi; Christine F McDonald; Allison L Collins; Ian A Darby; Dodie S Pouniotis
Journal:  World J Clin Oncol       Date:  2014-12-10

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  4 in total

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