Liebermann Dan A, Tront Jennifer S, Sha Xiogen, Mukherjee Ksushiki, Mohamed-Hadley Alisha, Hoffman Barbara
Fels Institute for Cancer Research and Molecular Biology, Temple University, Philadelphia, Pennsylvania 19140, USA.
Crit Rev Oncog. 2011;16(1-2):129-40. doi: 10.1615/critrevoncog.v16.i1-2.120.
Gadd45 proteins, including Gadd45a, Gadd45b, and Gadd45g, have been implicated in stress signaling in response to physiological and environmental stress, including oncogenic stress, which can result in cell cycle arrest, DNA repair, cell survival, senescence, and apoptosis. The function of Gadd45 as a stress sensor is mediated via a complex interplay of physical interactions with other cellular proteins implicated in cell cycle regulation and the response of cells to stress, notably PCNA, p21, cdc2/cyclinB1, and the p38 and JNK stress response kinases. Altered expression of Gadd45 has been observed in multiple types of solid tumors as well as in hematopoietic malignancies. Using genetically engineered mouse models and bone-marrow transplantation, evidence has been obtained indicating that Gadd45 proteins can function to either promote or suppress tumor development and leukemia; this is dependent on the molecular nature of the activated oncogene and the cell type, via engagement of different signaling pathways.
Gadd45蛋白,包括Gadd45a、Gadd45b和Gadd45g,参与了对生理和环境应激(包括致癌应激)的应激信号传导,这可能导致细胞周期停滞、DNA修复、细胞存活、衰老和凋亡。Gadd45作为应激传感器的功能是通过与其他参与细胞周期调节和细胞应激反应的细胞蛋白(特别是增殖细胞核抗原(PCNA)、p21、细胞周期蛋白依赖性激酶2/细胞周期蛋白B1(cdc2/cyclinB1)以及p38和JNK应激反应激酶)的复杂物理相互作用来介导的。在多种实体瘤以及血液系统恶性肿瘤中均观察到Gadd45表达改变。通过基因工程小鼠模型和骨髓移植,已获得证据表明,Gadd45蛋白可通过不同信号通路的参与,发挥促进或抑制肿瘤发展和白血病的作用;这取决于激活的癌基因的分子性质和细胞类型。