Togna G I, Togna A R, Franconi M, Caprino L
Department of Human Physiology and Pharmacology, University of Rome "La Sapienza," Italy.
Thromb Res. 2000 Sep 1;99(5):503-9. doi: 10.1016/s0049-3848(00)00294-2.
Clinical observations suggest that anticancer drugs could contribute to the thrombotic complications of malignancy in treated patients. Thrombotic microangiopathy, myocardial infarction, and cerebrovascular thrombotic events have been reported for cisplatin, a drug widely used in the treatment of many solid tumours. The aim of this study is to explore in vitro cisplatin effect on human platelet reactivity in order to define the potentially active role of platelets in the pathogenesis of cisplatin-induced thrombotic complications. Our results demonstrate that cisplatin increases human platelet reactivity (onset of platelet aggregation wave and thromboxane production) to non-aggregating concentrations of the agonists involving arachidonic acid metabolism. Direct or indirect activation of platelet phospholipase A(2) appears to be implicated. This finding contributes to a better understanding of the pathogenesis of thrombotic complications occurring during cisplatin-based chemotherapy.
临床观察表明,抗癌药物可能会导致接受治疗的患者出现恶性肿瘤的血栓并发症。血栓性微血管病、心肌梗死和脑血管血栓事件已被报道与顺铂有关,顺铂是一种广泛用于治疗多种实体肿瘤的药物。本研究的目的是探讨顺铂在体外对人血小板反应性的影响,以确定血小板在顺铂诱导的血栓并发症发病机制中可能发挥的作用。我们的结果表明,顺铂可使人类血小板对涉及花生四烯酸代谢的激动剂的非聚集浓度的反应性增加(血小板聚集波的起始和血栓素生成)。血小板磷脂酶A(2)的直接或间接激活似乎与之有关。这一发现有助于更好地理解基于顺铂的化疗过程中发生的血栓并发症的发病机制。