Lucotti Serena, Muschel Ruth J
Children's Cancer and Blood Foundation Laboratories, Departments of Pediatrics, and Cell and Developmental Biology, Drukier Institute for Children's Health, Meyer Cancer Center, Weill Cornell Medicine, New York, NY, United States.
Cancer Research UK and MRC Oxford Institute for Radiation Oncology, Department of Oncology, University of Oxford, Oxford, United Kingdom.
Front Oncol. 2020 Sep 18;10:1350. doi: 10.3389/fonc.2020.01350. eCollection 2020.
During the process of hematogenous metastasis, tumor cells interact with platelets and their precursors megakaryocytes, providing a selection driver for the metastatic phenotype. Cancer cells have evolved a plethora of mechanisms to engage platelet activation and aggregation. Platelet coating of tumor cells in the blood stream promotes the successful completion of multiple steps of the metastatic cascade. Along the same lines, clinical evidence suggests that anti-coagulant therapy might be associated with reduced risk of metastatic disease and better prognosis in cancer patients. Here, we review experimental and clinical literature concerning the contribution of platelets and megakaryocytes to cancer metastasis and provide insights into the clinical relevance of anti-coagulant therapy in cancer treatment.
在血行转移过程中,肿瘤细胞与血小板及其前体巨核细胞相互作用,为转移表型提供选择驱动因素。癌细胞已经进化出多种机制来促使血小板活化和聚集。肿瘤细胞在血流中的血小板包被促进了转移级联反应多个步骤的成功完成。同样,临床证据表明,抗凝治疗可能与降低癌症患者发生转移性疾病的风险及改善预后相关。在此,我们综述了关于血小板和巨核细胞对癌症转移作用的实验和临床文献,并深入探讨了抗凝治疗在癌症治疗中的临床相关性。