Identification of collapsin response mediator protein-2 as a potential marker of colorectal carcinoma by comparative analysis of cancer cell secretomes

被引:107
作者
Wu, Chih-Ching [2 ]
Chen, Hua-Chien
Chen, Su-Jen
Liu, Hao-Ping
Hsieh, Yi-Yueh [3 ,5 ]
Yu, Chia-Jung [1 ]
Tang, Reiping [4 ]
Hsieh, Ling-Ling
Yu, Jau-Song [1 ,2 ]
Chang, Yu-Sun
机构
[1] Chang Gung Univ, Dept Cell & Mol Biol, Tao Yuan, Taiwan
[2] Chang Gung Univ, Proteom Core Lab, Tao Yuan, Taiwan
[3] Chang Gung Mem Hosp, Dept Pathol, Tao Yuan, Taiwan
[4] Chang Gung Mem Hosp, Dept Surg, Colorectal Sect, Tao Yuan, Taiwan
[5] Chang Gung Univ, Dept Publ Hlth, Tao Yuan, Taiwan
关键词
CRMP-2; colorectal carcinoma; secretome; tumor marker;
D O I
10.1002/pmic.200700819
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The cancer cell secretome may contain many potentially useful biomarkers. We therefore sought to identify proteins in the conditioned media of colorectal carcinoma (CRC) cell lines but not in those from other cancer cell lines. The secretomes of 21 cancer cell lines derived from 12 cancer types were analyzed by SDS-PAGE combined with MALDI-TOF MS. Among the 325 proteins identified, collapsin response mediator protein-2 (CRMP-2) was chosen for evaluation as a potential CRC biomarker, since it was selectively detected in the CRC cell line secretome and has never been reported as a cancer biomarker. Immunohistochemical analysis of 169 CRC specimens showed that CRMP-2 was positively detected in 58.6% of the tumors, but weakly or not detected in > 90% of the adjacent nontumor epithelial cells. Moreover, the CRMP-2-positive rate was significantly increased in earlier stage tumors and lymph node metastasis. Plasma CRMP-2 levels were significantly higher in CRC patients (N = 201) versus healthy controls (N = 201) (61.3 +/- 34.6 vs. 40.2 +/- 24.3 ng/mL, p = 0.001). Our results indicate that comparative analysis of cancer cell secretome is a feasible strategy for identifying potential cancer biomarkers, and that CRMP-2 may be a novel CRC biomarker.
引用
收藏
页码:316 / 332
页数:17
相关论文
共 84 条
[1]  
Alessandro Riccardo, 2005, Clin Colorectal Cancer, V4, P396, DOI 10.3816/CCC.2005.n.012
[2]   Proteomic expression analysis of colorectal cancer by two-dimensional differential gel electrophoresis [J].
Alfonso, P ;
Núñez, A ;
Madoz-Gurpide, J ;
Lombardia, L ;
Sánchez, L ;
Casal, JI .
PROTEOMICS, 2005, 5 (10) :2602-2611
[3]   Genes of glycolysis are ubiquitously overexpressed in 24 cancer classes [J].
Altenberg, B ;
Greulich, KO .
GENOMICS, 2004, 84 (06) :1014-1020
[4]   Phosphorylation by Rho kinase regulates CRMP-2 activity in growth cones [J].
Arimura, N ;
Ménager, C ;
Kawano, Y ;
Yoshimura, T ;
Kawabata, S ;
Hattori, A ;
Fukata, Y ;
Amano, M ;
Goshima, Y ;
Inagaki, M ;
Morone, N ;
Usukura, J ;
Kaibuchi, K .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (22) :9973-9984
[5]  
Bast RC, 1998, J CLIN ONCOL, V16, P793
[6]   Feature-based prediction of non-classical and leaderless protein secretion [J].
Bendtsen, JD ;
Jensen, LJ ;
Blom, N ;
von Heijne, G ;
Brunak, S .
PROTEIN ENGINEERING DESIGN & SELECTION, 2004, 17 (04) :349-356
[7]   Improved prediction of signal peptides: SignalP 3.0 [J].
Bendtsen, JD ;
Nielsen, H ;
von Heijne, G ;
Brunak, S .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 340 (04) :783-795
[8]   Proteomic analysis of colorectal cancer reveals alterations in metabolic pathways - Mechanism of tumorigenesis [J].
Bi, Xuezhi ;
Lin, Qingsong ;
Foo, Tet Wei ;
Joshi, Shashikant ;
You, Tao ;
Shen, Han-Ming ;
Ong, Choon Nam ;
Cheah, Peh Yean ;
Eu, Kong Weng ;
Hew, Choy-Leong .
MOLECULAR & CELLULAR PROTEOMICS, 2006, 5 (06) :1119-1130
[9]  
Buckhaults P, 2001, CANCER RES, V61, P6996
[10]  
Byk T, 1996, J NEUROSCI, V16, P688