Wykosky Jill, Debinski Waldemar
Department of Neurosurgery, Brain Tumor Center of Excellence, Comprehensive Cancer Center of Wake Forest University, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157, USA.
Mol Cancer Res. 2008 Dec;6(12):1795-806. doi: 10.1158/1541-7786.MCR-08-0244.
The Eph receptor tyrosine kinases and ephrin ligands have been studied extensively for their roles in developmental processes. In recent years, Eph receptors and ephrins have been found to be integral players in cancer formation and progression. Among these are EphA2 and ephrinA1, which are involved in the development and maintenance of many different types of solid tumors. The function of EphA2 and ephrinA1 in tumorigenesis and tumor progression is complex and seems to be dependent on cell type and microenvironment. These variables affect the expression of the EphA2 and ephrinA1 proteins, the pathways through which they induce signaling, and the functional consequences of that signaling on the behavior of tumor cells and tumor-associated cells. This review will specifically focus on the roles that EphA2 and ephrinA1 play in the different cell types that contribute to the malignancy of solid tumors, with emphasis on the opportunities for therapeutic targeting.
Eph受体酪氨酸激酶和ephrin配体因其在发育过程中的作用而受到广泛研究。近年来,Eph受体和ephrins被发现是癌症形成和进展过程中的重要参与者。其中包括EphA2和ephrinA1,它们参与多种不同类型实体瘤的发生和维持。EphA2和ephrinA1在肿瘤发生和肿瘤进展中的功能复杂,似乎取决于细胞类型和微环境。这些变量会影响EphA2和ephrinA1蛋白的表达、它们诱导信号传导的途径,以及该信号传导对肿瘤细胞和肿瘤相关细胞行为的功能后果。本综述将特别关注EphA2和ephrinA1在促成实体瘤恶性肿瘤的不同细胞类型中所起的作用,重点是治疗靶点的机会。