Expression of developmentally regulated endothelial cell locus 1 was induced by tumor-derived factors including VEGF

被引:23
作者
Aoki, M [1 ]
Kanamori, M
Ohmori, K
Takaishi, M
Huh, NH
Nogami, S
Kimura, T
机构
[1] Toyama Med & Pharmaceut Univ, Dept Orthopaed Surg, Toyama, Japan
[2] Tokyo Womens Med Coll, Dept Orthopaed Surg, Tokyo 162, Japan
[3] Okayama Univ, Grad Sch Med & Dent, Dept Cell Biol, Okayama, Japan
关键词
developmentally regulated endothelial locus 1; vascular endothelial growth factor; angiogenesis; sarcoma; metastasis;
D O I
10.1016/j.bbrc.2005.06.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Developmentally regulated endothelial cell locus I (Del I) is a new angiogenic molecules expressed specifically in early embryonic endothelial cells. We investigated the relationship between Dell and tumor cell-derived vascular endothelial growth factor (VEGF). Dunn osteosarcoma cells and high- and low-metastatic murine sarcoma cells did not express Dell. However, the expression of Del I was observed in these primary tumor tissues and the pulmonary metastatic tissues after subcutaneous inoculation in vivo. Every tumor cell-conditioned medium containing VEGF induced the expression of Dell in murine lung microvascular endothelial (MLE) cells, although control MLE cells did not express Del I. The anti-mouse VEGF monoclonal antibody inhibited the induction of the Dell expression. In addition, mouse recombinant interleukin-lot and tumor necrosis factor-alpha also induced Dell in MLE cells. Dell may play an important role in tumor angiogenesis through the effects of tumor-derived factors including VEGF. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:990 / 995
页数:6
相关论文
共 40 条
[1]
The embryonic angiogenic factor Del1 accelerates tumor growth by enhancing vascular formation [J].
Aoka, Y ;
Johnson, FL ;
Penta, K ;
Hirata, K ;
Hidai, C ;
Schatzman, R ;
Varner, JA ;
Quertermous, T .
MICROVASCULAR RESEARCH, 2002, 64 (01) :148-161
[2]
Effects of vascular endothelial growth factor and E-selectin on angiogenesis in the murine metastatic RCT sarcoma [J].
Aoki, M ;
Kanamori, M ;
Yudoh, K ;
Ohmori, K ;
Yasuda, T ;
Kimura, T .
TUMOR BIOLOGY, 2001, 22 (04) :239-246
[3]
Asai T, 1998, INT J CANCER, V76, P418, DOI 10.1002/(SICI)1097-0215(19980504)76:3<418::AID-IJC21>3.3.CO
[4]
2-E
[5]
Migration of human monocytes in response to vascular endothelial growth factor (VEGF) is mediated via the VEGF receptor flt-1 [J].
Barleon, B ;
Sozzani, S ;
Zhou, D ;
Weich, HA ;
Mantovani, A ;
Marme, D .
BLOOD, 1996, 87 (08) :3336-3343
[6]
ORGAN-DERIVED MICROVESSEL ENDOTHELIAL-CELLS EXHIBIT DIFFERENTIAL RESPONSIVENESS TO THROMBIN AND OTHER GROWTH-FACTORS [J].
BELLONI, PN ;
CARNEY, DH ;
CARNEY, DH ;
NICOLSON, GL .
MICROVASCULAR RESEARCH, 1992, 43 (01) :20-45
[7]
INDUCTION OF VASCULAR ENDOTHELIAL GROWTH-FACTOR EXPRESSION IN SYNOVIAL FIBROBLASTS BY PROSTAGLANDIN-E AND INTERLEUKIN-1 - A POTENTIAL MECHANISM FOR INFLAMMATORY ANGIOGENESIS [J].
BENAV, P ;
CROFFORD, LJ ;
WILDER, RL ;
HLA, T .
FEBS LETTERS, 1995, 372 (01) :83-87
[8]
BREIER G, 1992, DEVELOPMENT, V114, P521
[9]
INTEGRIN ALPHA(V)BETA(3) ANTAGONISTS PROMOTE TUMOR-REGRESSION BY INDUCING APOPTOSIS OF ANGIOGENIC BLOOD-VESSELS [J].
BROOKS, PC ;
MONTGOMERY, AMP ;
ROSENFELD, M ;
REISFELD, RA ;
HU, TH ;
KLIER, G ;
CHERESH, DA .
CELL, 1994, 79 (07) :1157-1164
[10]
Claffey KP, 1996, CANCER RES, V56, P172