Is YKL-40 a new therapeutic target in cancer?

被引:61
作者
Johansen, Julia S.
Jensen, Benny Vittrup
Roslind, Anne
Price, Paul A.
机构
[1] Univ Copenhagen, Herlev Hosp, Dept Rheumatol Q107, DK-2730 Herlev, Denmark
[2] Univ Copenhagen, Herlev Hosp, Dept Oncol, DK-2730 Herlev, Denmark
[3] Univ Calif San Diego, Dept Biol, La Jolla, CA 92093 USA
关键词
biomarker; cancer target; CHI3L1; prognosis; YKL-40;
D O I
10.1517/14728222.11.2.219
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
YKL-40 is produced by cancer cells and tumour-associated macrophages. YKL-40 may play a role in cancer cell proliferation, differentiation, survival, invasiveness, metastasis, in angiogenesis and the inflammation and remodelling of the extracellular matrix surrounding the tumour. Serum YKL-40 is a biomarker of prognosis, confirmed in 13 different types of cancer including > 2500 patients. Highest serum YKL-40 is found in patients with metastatic cancer with the shortest recurrence-free interval and shortest overall survival. Serum YKL-40 provides independent information compared with clinical characteristics and biomarkers, such as HER2, carcinoembryonic antigen, CA-125, prostate-specific antigen and lactate dehydrogenase. The authors hypothesise that inhibition of YKL-40 by monoclonal antibodies either directly or towards its receptor may be as efficient a cancer therapeutic as the monoclonal antibodies against HER2, HER1, vascular endothelial growth factor and CD20. Drugs inhibiting YKL-40 should be explored as new cancer therapeutics.
引用
收藏
页码:219 / 234
页数:16
相关论文
共 147 条
[21]   Tumor-associated macrophages: The double-edged sword in cancer progression [J].
Chen, JJW ;
Lin, YC ;
Yao, PL ;
Yuan, A ;
Chen, HY ;
Shun, CT ;
Tsai, MF ;
Chen, CH ;
Yang, PC .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (05) :953-964
[22]   Serum YKL-40 and colorectal cancer [J].
Cintin, C ;
Johansen, JS ;
Christensen, IJ ;
Price, PA ;
Sorensen, S ;
Nielsen, HJ .
BRITISH JOURNAL OF CANCER, 1999, 79 (9-10) :1494-1499
[23]   High serum YKL-40 level after surgery for colorectal carcinoma is related to short survival [J].
Cintin, C ;
Johansen, JS ;
Christensen, IJ ;
Price, PA ;
Sorensen, S ;
Nielsen, HJ .
CANCER, 2002, 95 (02) :267-274
[24]   Inflammation and cancer [J].
Coussens, LM ;
Werb, Z .
NATURE, 2002, 420 (6917) :860-867
[25]   The synovial proteome: analysis of fibroblast-like synoviocytes [J].
Dasuri, K ;
Antonovici, M ;
Chen, KD ;
Wong, K ;
Standing, K ;
Ens, W ;
El-Gabalawy, H ;
Wilkins, JA .
ARTHRITIS RESEARCH & THERAPY, 2004, 6 (02) :R161-R168
[26]   Mechanism of glucocorticoid-induced depletion of human CD14+CD16+ monocytes [J].
Dayyani, F ;
Belge, KU ;
Frankenberger, M ;
Mack, M ;
Berki, T ;
Ziegler-Heitbrock, L .
JOURNAL OF LEUKOCYTE BIOLOGY, 2003, 74 (01) :33-39
[27]   YKL-40 (cartilage gp-39) induces proliferative events in cultured chondrocytes and synoviocytes and increases glycosaminoglycan synthesis in chondrocytes [J].
De Ceuninck, F ;
Gaufillier, S ;
Bonnaud, A ;
Sabatini, M ;
Lesur, C ;
Pastoureau, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 285 (04) :926-931
[28]  
De Ceuninck F, 1998, J CELL BIOCHEM, V69, P414, DOI 10.1002/(SICI)1097-4644(19980615)69:4<414::AID-JCB3>3.0.CO
[29]  
2-Q
[30]   Review - Proteases, extracellular matrix, and cancer - A workshop of the path B study section [J].
DeClerck, YA ;
Mercurio, AM ;
Stack, MS ;
Chapman, HA ;
Zutter, MM ;
Muschel, RJ ;
Raz, A ;
Matrisian, LM ;
Sloane, BF ;
Noel, A ;
Hendrix, MJ ;
Coussens, L ;
Padarathsingh, M .
AMERICAN JOURNAL OF PATHOLOGY, 2004, 164 (04) :1131-1139