Kaposi's sarcoma associated herpesvirus G protein-coupled receptor immortalizes human endothelial cells by activation of the VEGF receptor-2/KDR

被引:175
作者
Bais, C
Van Geelen, A
Eroles, P
Mutlu, A
Chiozzini, C
Dias, S
Silverstein, RL
Rafii, S
Mesri, EA
机构
[1] Cornell Univ, Weill Med Coll, Dept Med, Lab Viral Oncogenesis, New York, NY 10021 USA
[2] Cornell Univ, Weill Med Coll, Dept Med, Div Hematol Oncol, New York, NY 10021 USA
[3] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Biol, Doctorate Program Biol Sci, Buenos Aires, DF, Argentina
[4] Ist Super Sanita, Virol Lab, I-00161 Rome, Italy
关键词
D O I
10.1016/S1535-6108(03)00024-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The G protein-coupled receptor oncogene (vGPCR) of the Kaposi's sarcoma (KS) associated herpesvirus (KSHV), an oncovirus implicated in angioproliferative neoplasms, induces angiogenesis by VEGF secretion. Accordingly, we found that expression of vGPCR in human umbilical vein endothelial cells (HUVEC) leads to immortalization with constitutive VEGF receptor-2/ KDR expression and activation. vGPCR immortalization was associated with anti-senescence mediated by alternative lengthening of telomeres and an anti-apoptotic response mediated by vGPCR constitutive signaling and KDR autocrine signaling leading to activation of the PI3K/AKT pathway. In the presence of the KS growth factor VEGF, this mechanism can sustain suppression of signaling by the immortalizing gene. We conclude that vGPCR can cause an oncogenic immortalizing event and recapitulate aspects of the KS angiogenic phenotype in human endothelial cells, pointing to this gene as a pathogenic determinant of KSHV.
引用
收藏
页码:131 / 143
页数:13
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