Janes Peter W, Slape Christopher I, Farnsworth Rae H, Atapattu Lakmali, Scott Andrew M, Vail Mary E
Department of Biochemistry and Molecular Biology, Monash University , Victoria , Australia and.
Growth Factors. 2014 Dec;32(6):176-89. doi: 10.3109/08977194.2014.982276. Epub 2014 Nov 13.
Eph receptor tyrosine kinases control cell-cell interactions during normal and oncogenic development, and are implicated in a range of processes including angiogenesis, stem cell maintenance and metastasis. They are thus of great interest as targets for cancer therapy. EphA3, originally isolated from leukemic and melanoma cells, is presently one of the most promising therapeutic targets, with multiple tumor-promoting roles in a variety of cancer types. This review focuses on EphA3, its functions in controlling cellular behavior, both in normal and pathological development, and most particularly in cancer.
Eph受体酪氨酸激酶在正常和致癌发育过程中控制细胞间相互作用,并参与包括血管生成、干细胞维持和转移在内的一系列过程。因此,它们作为癌症治疗靶点备受关注。EphA3最初是从白血病细胞和黑色素瘤细胞中分离出来的,目前是最有前景的治疗靶点之一,在多种癌症类型中具有多种促进肿瘤的作用。这篇综述聚焦于EphA3,及其在正常和病理发育过程中,尤其是在癌症中控制细胞行为的功能。