Department of Pathology and Laboratory Medicine, Weill Cornell Medical College and Weill Graduate School of Medical Sciences of Cornell University New York, NY, USA.
Front Oncol. 2012 Mar 6;2:21. doi: 10.3389/fonc.2012.00021. eCollection 2012.
The cullin 4-RING ubiquitin ligase (CRL4) family employs multiple DDB1-CUL4 associated factors substrate receptors to direct the degradation of proteins involved in a wide spectrum of cellular functions. Aberrant expression of the cullin 4A (CUL4A) gene is found in many tumor types, while mutations of the cullin 4B (CUL4B) gene are causally associated with human X-linked mental retardation. This focused review will summarize our current knowledge of the two CUL4 family members in the pathogenesis of human malignancy and neuronal disease, and discuss their potential as new targets for cancer prevention and therapeutic intervention.
Cullin 4-RING 泛素连接酶(CRL4)家族利用多种 DDB1-CUL4 相关因子底物受体来指导涉及广泛细胞功能的蛋白质的降解。许多肿瘤类型中都发现了 Cullin 4A(CUL4A)基因的异常表达,而 Cullin 4B(CUL4B)基因突变则与人类 X 连锁智力迟钝有关。本综述将总结我们目前对 CUL4 家族这两个成员在人类恶性肿瘤和神经疾病发病机制中的认识,并讨论它们作为癌症预防和治疗干预新靶点的潜力。