Sikder Hashmat A, Devlin Meghann K, Dunlap Shariff, Ryu Byungwoo, Alani Rhoda M
The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.
Cancer Cell. 2003 Jun;3(6):525-30. doi: 10.1016/s1535-6108(03)00141-7.
Since the gene encoding Id1 was cloned in 1990, Id proteins have been implicated in regulating a variety of cellular processes, including cellular growth, senescence, differentiation, apoptosis, angiogenesis, and neoplastic transformation. The development of knockout and transgenic animal models for many members of the Id gene family has been particularly useful in sorting out the biologic relevance of these genes and their expression during normal development, malignant transformation, and tumor progression. Here we review the current understanding of Id gene function, the biologic consequences of Id gene expression, and the implications for Id gene regulation of cell growth and tumorigenesis.
自1990年编码Id1的基因被克隆以来,Id蛋白一直被认为参与调节多种细胞过程,包括细胞生长、衰老、分化、凋亡、血管生成和肿瘤转化。针对Id基因家族许多成员构建的基因敲除和转基因动物模型,对于厘清这些基因在正常发育、恶性转化和肿瘤进展过程中的生物学相关性及其表达情况特别有用。在此,我们综述了目前对Id基因功能的认识、Id基因表达的生物学后果,以及Id基因调控细胞生长和肿瘤发生的意义。