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Kaposi sarcoma herpesvirus-induced cellular reprogramming contributes to the lymphatic endothelial gene expression in Kaposi sarcoma

机译:卡波氏肉瘤疱疹病毒诱导的细胞重编程有助于卡波氏肉瘤中淋巴管内皮基因的表达

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The biology of Kaposi sarcoma is poorly understood because the dominant cell type in Kaposi sarcoma lesions is not known(1-4). We show by gene expression microarrays that neoplastic cells of Kaposi sarcoma are closely related to lymphatic endothelial cells (LECs) and that Kaposi sarcoma herpesvirus (KSHV)(5,6) infects both LECs and blood vascular endothelial cells (BECs) in vitro. The gene expression microarray profiles of infected LECs and BECs show that KSHV induces transcriptional reprogramming of both cell types. The lymphangiogenic molecules VEGF-D and angiopoietin-2 were elevated in the plasma of individuals with acquired immune deficiency syndrome and Kaposi sarcoma. These data show that the gene expression profile of Kaposi sarcoma resembles that of LECs, that KSHV induces a transcriptional drift in both LECs and BECs and that lymphangiogenic molecules are involved in the pathogenesis of Kaposi sarcoma.
机译:对卡波济肉瘤的生物学了解甚少,因为卡波济肉瘤病变中的优势细胞类型尚不清楚(1-4)。我们通过基因表达微阵列显示卡波西肉瘤的赘生性细胞与淋巴管内皮细胞(LECs)密切相关,并且卡波西肉瘤疱疹病毒(KSHV)(5,6)感染LECs和体外血管内皮细胞(BECs)。感染的LEC和BEC的基因表达微阵列谱显示,KSHV诱导两种细胞类型的转录重编程。患有获得性免疫缺陷综合症和卡波西肉瘤的个体血浆中的淋巴管生成分子VEGF-D和血管生成素2升高。这些数据表明,卡波济氏肉瘤的基因表达谱类似于LECs,KSHV诱导了LECs和BECs的转录漂移,并且淋巴管生成分子参与了卡波济氏肉瘤的发病机理。

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