IL-20, an anti-angiogenic cytokine that inhibits COX-2 expression

被引:35
作者
Heuzé-Vourc'h, N
Liu, M
Dalwadi, H
Baratelli, FE
Zhu, L
Goodglick, L
Pold, M
Sharma, S
Ramirez, RD
Shay, JW
Minna, JD
Strieter, RM
Dubinett, SM [1 ]
机构
[1] Univ Calif Los Angeles, Dept Med, Div Pulm & Crit Care Med, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Lung Canc Res Program, Los Angeles, CA USA
[3] Vet Affairs Greater Los Angeles Healthcare Ctr, Los Angeles, CA USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA USA
[5] Univ Texas, SW Med Ctr, Hamon Ctr Therapuet Oncol Res, Dallas, TX USA
[6] Dallas Vet Affairs Med Ctr, Dallas, TX USA
[7] Univ Texas, SW Med Ctr, Dept Cell Biol, Dallas, TX USA
关键词
interleukin-20; cyclooxygenase-2; prostaglandin-E-2; lung cancer; angiogenesis; NSCLC; human bronchial epithelial cells;
D O I
10.1016/j.bbrc.2005.05.122
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
COX-2 overexpression and subsequent PGE(2) production are frequently associated with non-small cell lung cancer and are implicated in tumor-mediated angiogenesis. Here, we report for the first time that IL-20 downregulates COX-2 and PGE(2) in human bronchial epithelial and endothelial cells. Flow cytometry analysis suggests that IL-20-dependent inhibition of COX-2/PGE(2) occurs through the IL-22R1/IL-2OR2 dimers. In addition, we report that IL-20 exerts anti-angiogenic effects, inhibiting experimental angiogenesis. IL-20-mediated inhibition of PMA-induced angiogenesis occurs through the COX-2 regulatory pathway. Altogether our findings revealed that IL-20 is a negative modulator of COX-2/PGE(2) and inhibits angiogenesis. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:470 / 475
页数:6
相关论文
共 21 条
[1]   Interleukin 20: Discovery, receptor identification, and role in epidermal function [J].
Blumberg, H ;
Conklin, D ;
Xu, WF ;
Grossmann, A ;
Brender, T ;
Carollo, S ;
Eagan, M ;
Foster, D ;
Haldeman, BA ;
Hammond, A ;
Haugen, H ;
Jelinek, L ;
Kelly, JD ;
Madden, K ;
Maurer, MF ;
Parrish-Novak, J ;
Prunkard, D ;
Sexson, S ;
Sprecher, C ;
Waggie, K ;
West, J ;
Whitmore, TE ;
Yao, L ;
Kuechle, MK ;
Dale, BA ;
Chandrasekher, YA .
CELL, 2001, 104 (01) :9-19
[2]   Lung cancer and cyclooxygenase-2 [J].
Castelao, JE ;
Bart, RD ;
DiPerna, CA ;
Sievers, EM ;
Bremner, RM .
ANNALS OF THORACIC SURGERY, 2003, 76 (04) :1327-1335
[3]   Signal transduction pathways regulating cyclooxygenase-2 expression: potential molecular targets for chemoprevention [J].
Chun, KS ;
Surh, YJ .
BIOCHEMICAL PHARMACOLOGY, 2004, 68 (06) :1089-1100
[4]   Targeting cyclooxygenase-2 in human neoplasia: Rationale and promise [J].
Dannenberg, AJ ;
Subbaramaiah, K .
CANCER CELL, 2003, 4 (06) :431-436
[5]   The contributions of cyclooxygenase-2 to tumor angiogenesis [J].
Gately, S .
CANCER AND METASTASIS REVIEWS, 2000, 19 (1-2) :19-27
[6]  
Herschman Harvey R, 2003, Mol Imaging Biol, V5, P286
[7]  
Heuze-Vourc'h N, 2003, CANCER RES, V63, P766
[8]   Cyclooxygenase-5: a target for the prevention and treatment of breast cancer [J].
Howe, LR ;
Subbaramaiah, K ;
Brown, AMC ;
Dannenberg, AJ .
ENDOCRINE-RELATED CANCER, 2001, 8 (02) :97-114
[9]  
Huang M, 1998, CANCER RES, V58, P1208
[10]  
HUANG M, 1995, CANCER RES, V55, P3847