c-fos-induced growth factor/vascular endothelial growth factor D induces angiogenesis in vivo and in vitro

被引:218
作者
Marconcini, L
Marchio, S
Morbidelli, L
Cartocci, E
Albini, A
Ziche, M
Bussolino, F
Oliviero, S
机构
[1] Univ Siena, Dipartimento Biol Mol, I-53100 Siena, Italy
[2] Univ Turin, Dipartimento Genet Biol & Chim Med, I-10060 Candiolo, Italy
[3] Inst Canc Res & Treatment, I-10060 Candiolo, Italy
[4] Univ Siena, Ist Sci Farmaceut, I-53100 Siena, Italy
[5] Univ Florence, Dipartimento Farmacol, I-50121 Florence, Italy
[6] Ist Nazl Ric Canc, I-16100 Genoa, Italy
[7] Ctr Biotecnol Avanzate, I-16100 Genoa, Italy
关键词
D O I
10.1073/pnas.96.17.9671
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
c-fos-induced growth factor/vascular endothelial growth factor D (Figf/Vegf-D) is a secreted factor of the VEGF family that binds to the vessel and lymphatic receptors VEGFR-2 and VEGFR-3, Here,ve report that Figf/Vegf-D is a potent angiogenic factor in rabbit cornea in vivo in a dose-dependent manner. In vitro Figf/Vegf-D induces tyrosine phosphorylation of VEGFR-2 and VEGFR-3 in primary human umbilical cord vein endothelial cells (HUVECs) and in an immortal cell line derived from Kaposi's sarcoma lesion (KS-IMM). The treatment of HUVECs with Figf/Vegf-D induces dose-dependent cell growth. Figf/VEGF-D also induces HUVEC elongation and branching to form an extensive network of capillary-like cords in three-dimensional matrix. In KS-IMM cells Figf/Vegf-D treatment results in dose-dependent mitogenic and motogenic activities. Taken together with the previous observations that Figf/Vegf-D expression is under the control of the nuclear oncogene c-fos, our data uncover a link between a nuclear oncogene and angiogenesis, suggesting that Figf/Vegf-D may play a critical role in tumor cell growth and invasion.
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页码:9671 / 9676
页数:6
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