Mandriota, SJ and Turner, KJ and Davies, DR and Murray, PG and Morgan, NV and Sowter, HM and Wykoff, CC and Maher, ER and Harris, AL and Ratcliffe, PJ and Maxwell, PH (2002) HIF activation identifies early lesions in VHL kidneys: Evidence for site-specific tumor suppressor function in the nephron. CANCER CELL , 1 (5) 459 - 468.
Full text not available from this repository.
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.
|Title:||HIF activation identifies early lesions in VHL kidneys: Evidence for site-specific tumor suppressor function in the nephron|
|Keywords:||RENAL-CELL CARCINOMA, HIPPEL-LINDAU GENE, HYPOXIA-INDUCIBLE FACTORS, FACTOR MESSENGER-RNA, GROWTH-FACTOR-ALPHA, LYMPHATIC CAPILLARIES, PROLINE HYDROXYLATION, PROLYL HYDROXYLATION, CARBONIC-ANHYDRASES, EXPRESSION|
|UCL classification:||UCL > School of Life and Medical Sciences > Faculty of Medical Sciences > Medicine (Division of)|
Archive Staff Only: edit this record