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Expression level of<scp>CXCL</scp>7in peripheral blood cells is a potential biomarker for the diagnosis of renal cell carcinoma

Authors :
Wataru Nakata
Kentaro Jingushi
Kazutoshi Fujita
Norio Nonomura
Toshiro Kinouchi
Ryoichi Imamura
Akira Nagahara
Motohide Uemura
Kyosuke Matsuzaki
Kaori Kitae
Yuko Ueda
Yoshiyuki Yamamoto
Cong Wang
Yu Ishizuya
Takuji Hayashi
Atsunari Kawashima
Takeshi Ujike
Takahiro Yoshida
Kazutake Tsujikawa
Source :
Cancer Science
Publication Year :
2017
Publisher :
Wiley, 2017.

Abstract

Summary There are no blood biomarkers for the diagnosis of renal cell carcinoma (RCC) in routine clinical use. We focused on the gene expression profile of peripheral blood cells obtained from RCC patients to discover novel biomarkers for RCC diagnosis. Using microarray analysis and quantitative verification, CXCL7 was shown to be significantly up-regulated in the peripheral blood cells of RCC patients. Importantly, aberrant CXCL7 expression was confirmed even in peripheral blood cells obtained from early stage (pT1a) RCC patients, and the expression level of CXCL7 in peripheral blood cells was a potential independent biomarker for the diagnosis of RCC by Receiver Operating Characteristic curve analysis (sensitivity of 70.0% and specificity of 64.0%, AUC = 0.722, a multiple logistic regression analysis, OR, 1.07; 95% CI, 1.03–1.11; P = 0.0004). Moreover, CXCL7 expression in peripheral blood cells significantly decreased after resection of the primary tumor. CXCL7 is more highly expressed in peripheral blood mononuclear cells than in neutrophils from both healthy controls and RCC patients. Interestingly, CXCL7 expression in peripheral blood mononuclear cells from healthy volunteers was significantly elevated following co-culture with RCC cells compared to those co-cultured with normal cells as a control. These results suggest that aberrant CXCL7 expression in peripheral blood cells is induced by RCC cells and may serve as a novel biomarker in the diagnosis of RCC. This article is protected by copyright. All rights reserved.

Details

ISSN :
13497006 and 13479032
Volume :
108
Database :
OpenAIRE
Journal :
Cancer Science
Accession number :
edsair.doi.dedup.....29b986a116ed70840512f6935540f2bb