Bais C, Santomasso B, Coso O, Arvanitakis L, Raaka E G, Gutkind J S, Asch A S, Cesarman E, Gershengorn M C, Mesri E A
Laboratory of Viral Oncogenesis, Division of Hematology-Oncology, Cornell University Medical College, New York, New York 10021, USA.
Nature. 1998 Jan 1;391(6662):86-9. doi: 10.1038/34193.
The Kaposi's sarcoma-associated herpesvirus (KSHV/HHV8) is a gamma-2 herpesvirus that is implicated in the pathogenesis of Kaposi's sarcoma and of primary effusion B-cell lymphomas (PELs). KSHV infects malignant and progenitor cells of Kaposi's sarcoma and PEL, it encodes putative oncogenes and genes that may cause Kaposi's sarcoma pathogenesis by stimulating angiogenesis. The G-protein-coupled receptor encoded by an open reading frame (ORF 74) of KSHV is expressed in Kaposi's sarcoma lesions and in PEL and stimulates signalling pathways linked to cell proliferation in a constitutive (agonist-independent) way. Here we show that signalling by this KSHV G-protein-coupled receptor leads to cell transformation and tumorigenicity, and induces a switch to an angiogenic phenotype mediated by vascular endothelial growth factor, an angiogenesis and Kaposi's-spindle-cell growth factor. We find that this receptor can activate two protein kinases, JNK/SAPK and p38MAPK, by triggering signalling cascades like those induced by inflammatory cytokines that are angiogenesis activators and mitogens for Kaposi's sarcoma cells and B cells. We conclude that the KSHV G-protein-coupled receptor is a viral oncogene that can exploit cell signalling pathways to induce transformation and angiogenesis in KSHV-mediated oncogenesis.
卡波西肉瘤相关疱疹病毒(KSHV/HHV8)是一种γ-2疱疹病毒,与卡波西肉瘤和原发性渗出性B细胞淋巴瘤(PEL)的发病机制有关。KSHV感染卡波西肉瘤和PEL的恶性细胞及祖细胞,它编码假定的癌基因以及可能通过刺激血管生成导致卡波西肉瘤发病机制的基因。由KSHV的一个开放阅读框(ORF 74)编码的G蛋白偶联受体在卡波西肉瘤病变和PEL中表达,并以组成性(不依赖激动剂)方式刺激与细胞增殖相关的信号通路。在此我们表明,这种KSHV G蛋白偶联受体发出的信号导致细胞转化和致瘤性,并诱导向由血管内皮生长因子介导的血管生成表型转变,血管内皮生长因子是一种血管生成因子和卡波西肉瘤纺锤体细胞生长因子。我们发现该受体可通过触发类似于由炎症细胞因子诱导的信号级联反应来激活两种蛋白激酶,即JNK/SAPK和p38MAPK,炎症细胞因子是血管生成激活剂以及卡波西肉瘤细胞和B细胞的有丝分裂原。我们得出结论,KSHV G蛋白偶联受体是一种病毒癌基因,其可利用细胞信号通路在KSHV介导的肿瘤发生过程中诱导转化和血管生成。