Kuehn E Wolfgang, Walz Gerd, Benzing Thomas
Renal Division, University Hospital Freiburg, Freiburg, Germany.
Cancer Res. 2007 May 15;67(10):4537-40. doi: 10.1158/0008-5472.CAN-07-0391.
Loss of von Hippel-Lindau (VHL) tumor suppressor gene function occurs in familial and most sporadic renal cell carcinoma. The tumor suppressor role of the protein pVHL is based on its ability to target transcription factors of the hypoxia-inducible factor family for degradation, but other functions of pVHL are less clearly defined. New findings show that pVHL is necessary for cilia formation. pVHL interacts with PAR proteins, a complex that specifies the membrane domains of polarized epithelial cells, and directs the orientation of growing microtubules. Loss of pVHL results in aberrant orientation of newly formed microtubules and prevents ciliogenesis. These results add to a growing body of evidence linking cilia and the cell cycle and suggest that the tumor suppressor role of pVHL may involve previously unrecognized pathways.
在家族性和大多数散发性肾细胞癌中,都会出现冯·希佩尔-林道(VHL)肿瘤抑制基因功能的丧失。蛋白质pVHL的肿瘤抑制作用基于其靶向缺氧诱导因子家族转录因子进行降解的能力,但其其他功能尚不太明确。新发现表明,pVHL对纤毛形成是必需的。pVHL与PAR蛋白相互作用,PAR蛋白是一种确定极化上皮细胞膜结构域的复合物,并指导生长中的微管的方向。pVHL的缺失导致新形成的微管方向异常,并阻止纤毛发生。这些结果进一步证明了纤毛与细胞周期之间的联系,并表明pVHL的肿瘤抑制作用可能涉及以前未被认识的途径。