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Clinical significance of serum thymus and activation-regulated chemokine in gastric cancer: Potential as a serum biomarker

Authors
 Jong-Baeck Lim  ;  Do-Kyun Kim  ;  Hye Won Chung 
Citation
 CANCER SCIENCE, Vol.105(10) : 1327-1333, 2014 
Journal Title
CANCER SCIENCE
ISSN
 1347-9032 
Issue Date
2014
MeSH
Biomarkers, Tumor/blood* ; CA-19-9 Antigen/blood ; Carcinoembryonic Antigen/blood ; Chemokine CCL17/blood* ; Chemokine CCL2/blood ; Chemokine CCL22/blood ; Humans ; Logistic Models ; Stem Cell Factor/blood ; Stomach Neoplasms/blood ; Stomach Neoplasms/diagnosis* ; Stomach Neoplasms/pathology
Keywords
Diagnostic ; gastric cancer ; prognostic ; serum biomarker ; thymus and activation-regulated chemokine
Abstract
Thymus and activation-regulated chemokine (TARC) can stimulate cancer cell proliferation and migration. The present study evaluated the clinical significance of serum TARC in gastric cancer (GC). We measured serum TARC, macrophage-derived chemokine, monocyte chemotactic protein-1 and stem cell factor (SCF) levels using a chemiluminescent immunoassay along the GC carcinogenesis (normal, high-risk, early GC [EGC] and advanced GC [AGC]) in both training (N = 25 per group) and independent validation datasets (90 normal, 30 high-risk, 50 EGC and 50 AGC). Serum levels were compared among groups using one-way analysis of variance. To evaluate the diagnostic potential of serum TARC for GC, receiver operating characteristic curve and logistic regression analyses were performed. Correlations between serum TARC and GC clinicopathological features were analyzed using Spearman's correlation. In the training dataset, serum TARC correlated with serum MDC, MCP-1 and SCF. However, only serum TARC and SCF were significantly higher in cancer groups than non-cancer groups (P < 0.001). In the validation dataset, serum TARC also increased along the GC carcinogenesis; the AGC group (167.2 ± 111.1 ng/mL) had significantly higher levels than the EGC (109.1 ± 67.7 ng/mL), the high-risk (66.2 ± 47.7 ng/mL) and the normal (67.5 ± 36.2 ng/mL) groups (Bonferroni, all P < 0.001). Receiver operating characteristic curves and logistic regression demonstrated the remarkable diagnostic potential of serum TARC as a single marker (72.0% sensitivity and 71.1% specificity; cutoff point, 0.37; logistic regression) and in a multiple-marker panel (72.6% sensitivity and 88.2% specificity; cutoff point, 0.54). Spearman's correlation showed that serum TARC was closely correlated with tumor size (γs = 0.227, P = 0.028), T-stage (γs = 0.340, P = 0.001), N-stage (γs = 0.318, P = 0.002) and M-stage (γs = 0.346, P = 0.001). Serum TARC is a promising serum biomarker for GC.
Full Text
http://onlinelibrary.wiley.com/doi/10.1111/cas.12505/abstract
DOI
10.1111/cas.12505
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers
Yonsei Authors
Lim, Jong Baeck(임종백) ORCID logo https://orcid.org/0000-0003-0419-0422
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/100186
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