Kaelin William G
Howard Hughes Medical Institute, Dana-Farber Cancer Institute, and Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Am Soc Nephrol. 2003 Nov;14(11):2703-11. doi: 10.1097/01.asn.0000092803.69761.41.
Recent studies of a relatively rare hereditary cancer syndrome, von Hippel-Lindau (VHL) disease, have shed new light on the molecular pathogenesis of kidney cancer and, perhaps more important, on how mammalian cells sense and respond to changes in oxygen availability. This knowledge is already translating into new therapeutic targets for kidney cancer as well as for multiple conditions, such as myocardial infarction and stroke, in which ischemia plays a pathogenic role. This review summarizes the current knowledge of the molecular pathogenesis of von Hippel-Lindau disease and the role of the VHL gene product (pVHL) in kidney cancer and the mammalian oxygen sensing pathway.
最近对一种相对罕见的遗传性癌症综合征——冯·希佩尔-林道(VHL)病的研究,为肾癌的分子发病机制,或许更重要的是,为哺乳动物细胞如何感知并应对氧可用性的变化,带来了新的认识。这一知识已转化为肾癌以及多种病症(如心肌梗死和中风,其中局部缺血起致病作用)的新治疗靶点。本综述总结了目前关于冯·希佩尔-林道病分子发病机制的知识,以及VHL基因产物(pVHL)在肾癌和哺乳动物氧感应途径中的作用。