Flamme I, Krieg M, Plate K H
Zentrum für Molekularbiologische Medizin, Universität zu Köln, Germany.
Am J Pathol. 1998 Jul;153(1):25-9. doi: 10.1016/s0002-9440(10)65541-1.
Hemangioblastomas, the most frequent manifestation of the hereditary von Hippel-Lindau disease (VHL), are highly vascularized tumors of the central nervous system. In previous studies, the endothelial-specific mitogen vascular endothelial growth factor (VEGF) was shown to be up-regulated in the stromal cells, the putative neoplastic cells in hemangioblastomas. Therefore, it was suggested that secretion of VEGF by stromal cells is the pathogenetic cause of the vascular lesions in hemangioblastomas. The novel basic helix loop helix transcription factor HRF/HIF-2alpha is a candidate regulator of VEGF expression during development. We therefore investigated expression of HRF/HIF-2alpha in hemangioblastomas and found the overexpression of VEGF mRNA in stromal cells to be highly correlated with elevated expression levels of HRF/HIF-2alpha mRNA. This finding is suggestive for a role of HRF in VEGF-dependent vascular growth in hemangioblastomas and could provide a link between transcriptional activation of the VEGF gene and loss of function of the VHL gene product.
血管母细胞瘤是遗传性冯·希佩尔-林道病(VHL)最常见的表现形式,是中枢神经系统的高度血管化肿瘤。在先前的研究中,内皮细胞特异性促有丝分裂原血管内皮生长因子(VEGF)在血管母细胞瘤的基质细胞(即假定的肿瘤细胞)中被证明上调。因此,有人提出基质细胞分泌VEGF是血管母细胞瘤血管病变的致病原因。新型碱性螺旋环螺旋转录因子HRF/HIF-2α是发育过程中VEGF表达的候选调节因子。因此,我们研究了HRF/HIF-2α在血管母细胞瘤中的表达,发现基质细胞中VEGF mRNA的过表达与HRF/HIF-2α mRNA表达水平的升高高度相关。这一发现提示HRF在血管母细胞瘤中VEGF依赖性血管生长中起作用,并可能在VEGF基因的转录激活与VHL基因产物的功能丧失之间提供联系。