Coexpression of EphB4 and ephrinB2 in tumour advancement of ovarian cancers

被引:50
作者
Alam, S. M. [1 ]
Fujimoto, J. [1 ]
Jahan, I. [1 ]
Sato, E. [1 ]
Tamaya, T. [1 ]
机构
[1] Gifu Univ, Sch Med, Dept Obstet & Gynecol, Gifu 5011194, Japan
关键词
EphB4; ephrinB2; prognostic indicator; tumour advancement; ovarian cancers;
D O I
10.1038/sj.bjc.6604216
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
EphB4 and ephrinB2 expressions in ovarian cancers were studied to analyse EphB4/ephrinB2 functions against clinical backgrounds. EphB4 and ephrinB2 were dominantly localised in ovarian cancer cells of all cases studied. Both the histoscores and mRNA levels of EphB4 and ephrinB2 significantly increased with clinical stages (I<II<III<IV, P < 0.001) in ovarian cancers, although there was no significant difference in EphB4 and ephrinB2 histoscores or in mRNA levels according to histopathological types. EphB4 as well as ephrinB2 histoscores in cancer cells correlated with the corresponding mRNA levels in each case (EphB4, P < 0.001; ephrinB2, P < 0.001). The 24-month survival rates of the 36 patients with high EphB4 and ephrinB2 expression were poor (25 and 27%, respectively), while for the other 36 patients with low EphB4 and ephrinB2 expression, they were significantly higher (68 and 64%, respectively). Therefore, EphB4/ephrinB2 may function in tumour advancement and coexpression of the Eph/ephrin system may potentiate tumour progression leading to poor survival. Thus, EphB4/ephrinB2 can be recognised as a novel prognostic indicator in the primary tumours of ovarian cancers.
引用
收藏
页码:845 / 851
页数:7
相关论文
共 44 条
[1]
Overexpression of ephrinB2 and EphB4 in tumor advancement of uterine endometrial cancers [J].
Alam, S. M. ;
Fujimoto, J. ;
Jahan, I. ;
Sato, E. ;
Tamaya, T. .
ANNALS OF ONCOLOGY, 2007, 18 (03) :485-490
[2]
[Anonymous], INT J GYNECOL OBSTET
[3]
MEMBRANE-BOUND LERK2 LIGAND CAN SIGNAL THROUGH 3 DIFFERENT EPH-RELATED RECEPTOR TYROSINE KINASES [J].
BRAMBILLA, R ;
SCHNAPP, A ;
CASAGRANDA, F ;
LABRADOR, JP ;
BERGEMANN, AD ;
FLANAGAN, JG ;
PASQUALE, EB ;
KLEIN, R .
EMBO JOURNAL, 1995, 14 (13) :3116-3126
[4]
Soluble Eph A receptors inhibit tumor angiogenesis and progression in vivo [J].
Brantley, DM ;
Cheng, N ;
Thompson, EJ ;
Lin, Q ;
Brekken, RA ;
Thorpe, PE ;
Muraoka, RS ;
Cerretti, DP ;
Pozzi, A ;
Jackson, D ;
Lin, C ;
Chen, J .
ONCOGENE, 2002, 21 (46) :7011-7026
[5]
New potential ligand-receptor signaling loops in ovarian cancer identified in multiple gene expression studies [J].
Castellano, Giancarlo ;
Reid, James F. ;
Alberti, Paola ;
Carcangiu, Maria Luisa ;
Tomassetti, Antonella ;
Canevari, Silvana .
CANCER RESEARCH, 2006, 66 (22) :10709-10719
[6]
Ephrin B expression in epithelial ovarian neoplasms correlates with tumor differentiation and angiogenesis [J].
Castellvi, Josep ;
Garcia, Angel ;
de la Torre, Javier ;
Hernandez, Javier ;
Gil, Antonio ;
Xercavins, Jordi ;
Ramon y Cajal, Santiago .
HUMAN PATHOLOGY, 2006, 37 (07) :883-889
[7]
Cheng N, 2002, MOL CANCER RES, V1, P2
[8]
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P159
[9]
LIGANDS FOR EPH-RELATED RECEPTOR TYROSINE KINASES THAT REQUIRE MEMBRANE ATTACHMENT OR CLUSTERING FOR ACTIVITY [J].
DAVIS, S ;
GALE, NW ;
ALDRICH, TH ;
MAISONPIERRE, PC ;
LHOTAK, V ;
PAWSON, T ;
GOLDFARB, M ;
YANCOPOULOS, GD .
SCIENCE, 1994, 266 (5186) :816-819
[10]
Eph receptors and ephrin ligands: embryogenesis to tumorigenesis [J].
Dodelet, VC ;
Pasquale, EB .
ONCOGENE, 2000, 19 (49) :5614-5619