Hascoet Pauline, Chesnel Franck, Le Goff Cathy, Le Goff Xavier, Arlot-Bonnemains Yannick
UMR 6290 (IGDR), CNRS, University Rennes-1 , Rennes , France.
Front Oncol. 2015 Oct 27;5:241. doi: 10.3389/fonc.2015.00241. eCollection 2015.
Human tumors exhibit a variety of genetic alterations, including point mutations, translocations, gene amplifications and deletions, as well as aneuploid chromosome numbers. For carcinomas, aneuploidy is associated with poor patient outcome for a large variety of tumor types, including breast, colon, and renal cell carcinoma. The Renal cell carcinoma (RCC) is a heterogeneous carcinoma consisting of different histologic types. The clear renal cell carcinoma (ccRCC) is the most common subtype and represents 85% of the RCC. Central to the biology of the ccRCC is the loss of function of the Von Hippel-Lindau gene, but is also associated with genetic instability that could be caused by abrogation of the cell cycle mitotic spindle checkpoint and may involve the Aurora kinases, which regulate centrosome maturation. Aneuploidy can also result from the loss of cell-cell adhesion and apical-basal cell polarity that also may be regulated by the mitotic kinases (polo-like kinase 1, casein kinase 2, doublecortin-like kinase 1, and Aurora kinases). In this review, we describe the "non-mitotic" unconventional functions of these kinases in renal tumorigenesis.
人类肿瘤表现出多种基因改变,包括点突变、易位、基因扩增和缺失,以及非整倍体染色体数目。对于癌来说,非整倍体与多种肿瘤类型(包括乳腺癌、结肠癌和肾细胞癌)患者的不良预后相关。肾细胞癌(RCC)是一种由不同组织学类型组成的异质性癌。透明肾细胞癌(ccRCC)是最常见的亚型,占RCC的85%。ccRCC生物学的核心是冯·希佩尔-林道基因功能的丧失,但也与遗传不稳定性有关,这种不稳定性可能由细胞周期有丝分裂纺锤体检查点的废除引起,并且可能涉及调节中心体成熟的极光激酶。非整倍体也可能源于细胞间粘附和顶端-基底端细胞极性的丧失,而这也可能受有丝分裂激酶(polo样激酶1、酪蛋白激酶2、双皮质素样激酶1和极光激酶)的调节。在本综述中,我们描述了这些激酶在肾肿瘤发生中的“非有丝分裂”非常规功能。