Mandriota Stefano J, Turner Kevin J, Davies David R, Murray Paul G, Morgan Neil V, Sowter Heidi M, Wykoff Charles C, Maher Eamonn R, Harris Adrian L, Ratcliffe Peter J, Maxwell Patrick H
Wellcome Trust Centre for Human Genetics, Oxford OX3 7BN, United Kingdom.
Cancer Cell. 2002 Jun;1(5):459-68. doi: 10.1016/s1535-6108(02)00071-5.
Mutations in the von Hippel-Lindau (VHL) gene are associated with hereditary and sporadic clear cell renal carcinoma. VHL acts in a ubiquitin ligase complex regulating hypoxia-inducible factor-1 (HIF-1), but the link between this function and cancer development is unclear. Here we show that in the kidneys of patients with VHL disease, HIF activation is an early event occurring in morphologically normal single cells within the renal tubules. In comparison, dysplastic lesions, cystic lesions, and tumors showed evidence of additional mechanisms that amplify HIF activation. Detection of cells with constitutive HIF activation identified a large number of previously unrecognized foci of VHL inactivation. In proximal tubules these were almost entirely unicellular, whereas multicellular foci were almost exclusively seen in the distal nephron.
冯·希佩尔-林道(VHL)基因的突变与遗传性和散发性透明细胞肾细胞癌相关。VHL在一种调节缺氧诱导因子-1(HIF-1)的泛素连接酶复合物中发挥作用,但这种功能与癌症发展之间的联系尚不清楚。在此我们表明,在VHL病患者的肾脏中,HIF激活是在肾小管内形态正常的单个细胞中发生的早期事件。相比之下,发育异常病变、囊性病变和肿瘤显示出放大HIF激活的其他机制的证据。对具有组成性HIF激活的细胞的检测确定了大量以前未被识别的VHL失活灶。在近端小管中,这些几乎完全是单细胞的,而多细胞灶几乎仅见于远端肾单位。