Meikle Claire K S, Kelly Clare A, Garg Priyanka, Wuescher Leah M, Ali Ramadan A, Worth Randall G
Department of Medical Microbiology and Immunology, University of Toledo College of Medicine and Life Sciences Toledo, OH, USA.
Front Cell Dev Biol. 2017 Jan 5;4:147. doi: 10.3389/fcell.2016.00147. eCollection 2016.
Platelets are critical to hemostatic and immunological function, and are key players in cancer progression, metastasis, and cancer-related thrombosis. Platelets interact with immune cells to stimulate anti-tumor responses and can be activated by immune cells and tumor cells. Platelet activation can lead to complex interactions between platelets and tumor cells. Platelets facilitate cancer progression and metastasis by: (1) forming aggregates with tumor cells; (2) inducing tumor growth, epithelial-mesenchymal transition, and invasion; (3) shielding circulating tumor cells from immune surveillance and killing; (4) facilitating tethering and arrest of circulating tumor cells; and (5) promoting angiogenesis and tumor cell establishment at distant sites. Tumor cell-activated platelets also predispose cancer patients to thrombotic events. Tumor cells and tumor-derived microparticles lead to thrombosis by secreting procoagulant factors, resulting in platelet activation and clotting. Platelets play a critical role in cancer progression and thrombosis, and markers of platelet-tumor cell interaction are candidates as biomarkers for cancer progression and thrombosis risk.
血小板对止血和免疫功能至关重要,并且是癌症进展、转移及癌症相关血栓形成的关键参与者。血小板与免疫细胞相互作用以刺激抗肿瘤反应,并且可被免疫细胞和肿瘤细胞激活。血小板活化可导致血小板与肿瘤细胞之间发生复杂的相互作用。血小板通过以下方式促进癌症进展和转移:(1)与肿瘤细胞形成聚集体;(2)诱导肿瘤生长、上皮-间质转化和侵袭;(3)保护循环肿瘤细胞免受免疫监视和杀伤;(4)促进循环肿瘤细胞的黏附和滞留;以及(5)促进远处部位的血管生成和肿瘤细胞定植。肿瘤细胞激活的血小板还使癌症患者易发生血栓事件。肿瘤细胞和肿瘤衍生的微粒通过分泌促凝血因子导致血栓形成,从而引起血小板活化和凝血。血小板在癌症进展和血栓形成中起关键作用,血小板-肿瘤细胞相互作用的标志物有望作为癌症进展和血栓形成风险的生物标志物。