Eph receptors and ephrins in cancer progression

促红细胞生成素肝细胞(Eph)受体 以法林 EPH受体A2 癌症研究 血管生成 癌细胞 生物 癌症 转移 受体酪氨酸激酶 癌症干细胞 受体 细胞生物学 信号转导 干细胞 遗传学
作者
Elena B. Pasquale
出处
期刊:Nature Reviews Cancer [Nature Portfolio]
卷期号:24 (1): 5-27 被引量:48
标识
DOI:10.1038/s41568-023-00634-x
摘要

Evidence implicating Eph receptor tyrosine kinases and their ephrin ligands (that together make up the 'Eph system') in cancer development and progression has been accumulating since the discovery of the first Eph receptor approximately 35 years ago. Advances in the past decade and a half have considerably increased the understanding of Eph receptor–ephrin signalling mechanisms in cancer and have uncovered intriguing new roles in cancer progression and drug resistance. This Review focuses mainly on these more recent developments. I provide an update on the different mechanisms of Eph receptor–ephrin-mediated cell–cell communication and cell autonomous signalling, as well as on the interplay of the Eph system with other signalling systems. I further discuss recent advances in elucidating how the Eph system controls tumour expansion, invasiveness and metastasis, supports cancer stem cells, and drives therapy resistance. In addition to functioning within cancer cells, the Eph system also mediates the reciprocal communication between cancer cells and cells of the tumour microenvironment. The involvement of the Eph system in tumour angiogenesis is well established, but recent findings also demonstrate roles in immune cells, cancer-associated fibroblasts and the extracellular matrix. Lastly, I discuss strategies under evaluation for therapeutic targeting of Eph receptors–ephrins in cancer and conclude with an outlook on promising future research directions. This Review by Elena B. Pasquale outlines the current understanding of Eph receptor–ephrin signalling mechanisms in cancer progression and therapy resistance, and also details therapeutic strategies for targeting the Eph system as a novel cancer therapy and for improving the efficacy of conventional cancer therapies.
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