Identification of Kininogen-1 as a Serum Biomarker for the Early Detection of Advanced Colorectal Adenoma and Colorectal Cancer

被引:7
|
作者
Wang, Jing [1 ,2 ]
Wang, Xinying [1 ,2 ]
Lin, Shiyong [3 ]
Chen, Chudi [1 ,2 ]
Wang, Congrong [4 ]
Ma, Qunying [1 ,2 ]
Jiang, Bo [1 ,2 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Gastroenterol, Guangzhou, Guangdong, Peoples R China
[2] Guangdong Prov Key Lab Gastroenterol, Guangzhou, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Ctr Canc, Dept Endoscopy & Laser, Guangzhou 510275, Guangdong, Peoples R China
[4] Southern Med Univ, Nanfang Hosp, Dept Lab Med, Guangzhou, Guangdong, Peoples R China
来源
PLOS ONE | 2013年 / 8卷 / 07期
关键词
FECAL OCCULT BLOOD; CELL CARCINOMA; PRACTICE GUIDELINES; MASS-SPECTROMETRY; TUMOR-MARKERS; IN-VIVO; PROTEOMICS; PLASMA; RISK; EXPRESSION;
D O I
10.1371/journal.pone.0070519
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Serum markers represent potential tools for the detection of colorectal cancer (CRC). The aim of this study was to obtain proteomic expression profiles and identify serum markers for the early detection of CRC. Methods: Proteomic profiles of serum samples collected from 35 healthy volunteers, 35 patients with advanced colorectal adenoma (ACA), and 40 patients with CRC were compared using Clinprot technology. Using enzyme-linked immunosorbent assays (ELISAs), 366 sera samples were additionally analyzed, and immunohistochemistry studies of 400 tissues were used to verify the expression of kininogen-1 and its value in the early detection of CRC. Results: Predicting models were established among the three groups, and kininogen-1 was identified as a potential marker for CRC using Clinprot technology. ELISAs also detected significantly higher serum kininogen-1 levels in ACA and CRC patients compared to controls (P<0.05). Furthermore, the area under the receiver operating characteristic curve (AUC) for serum kininogen-1 in the diagnosis of ACA was 0.635 (P = 0.003), and for serum carcinoembryonic antigen (CEA) was 0.453 (P = 0.358). The sensitivity, specificity, and accuracy of serum kininogen-1 for diagnosing Duke's stage A and B CRC was 70.13%, 65.88%, and 67.90%, respectively, whereas serum CEA was 38.96%, 85.88%, and 63.58%, respectively. Moreover, immunohistochemistry showed that expression of kininogen-1 was significantly higher in CRC and ACA tissues than in normal mucosa (48.39% vs. 15.58% vs. 0%, P<0.05). Conclusions: These results suggest that Clinprot technology provides a useful tool for the diagnosis of CRC, and kininogen-1 is a potential serum biomarker for the early detection of advanced colorectal adenoma and CRC.
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页数:9
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