pubmed-article:12388718 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:12388718 | lifeskim:mentions | umls-concept:C0036220 | lld:lifeskim |
pubmed-article:12388718 | lifeskim:mentions | umls-concept:C0029016 | lld:lifeskim |
pubmed-article:12388718 | lifeskim:mentions | umls-concept:C0302600 | lld:lifeskim |
pubmed-article:12388718 | lifeskim:mentions | umls-concept:C0079633 | lld:lifeskim |
pubmed-article:12388718 | lifeskim:mentions | umls-concept:C2003941 | lld:lifeskim |
pubmed-article:12388718 | lifeskim:mentions | umls-concept:C0086597 | lld:lifeskim |
pubmed-article:12388718 | pubmed:issue | 22 | lld:pubmed |
pubmed-article:12388718 | pubmed:dateCreated | 2002-10-21 | lld:pubmed |
pubmed-article:12388718 | pubmed:abstractText | The development of the complex neoplasm Kaposi's sarcoma is dependent on infection with the Kaposi's sarcoma-associated herpesvirus (KSHV) and appears to be greatly enhanced by cytokines and human immunodeficiency virus type 1 (HIV-1) Tat. Interleukin-8 (IL-8) and growth-regulated oncogene alpha (GRO-alpha) are chemokines involved in chemoattraction, neovascularization, and stimulation of HIV-1 replication. We have previously demonstrated that production of GRO-alpha is stimulated by exposure of monocyte-derived macrophages (MDM) to HIV-1. Here we show that exposure of MDM to HIV-1, viral Tat, or viral gp120 leads to a substantial increase in IL-8 production. We also demonstrate that IL-8 and GRO-alpha are induced by KSHV infection of endothelial cells and are crucial to the angiogenic phenotype developed by KSHV-infected endothelial cells in cell culture and upon implantation into SCID mice. Thus, the three known etiological factors in Kaposi's sarcoma pathogenesis-KSHV, HIV-1 Tat, and cellular growth factors-might be linked, in part, through induction of IL-8 and GRO-alpha. | lld:pubmed |
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