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CXCL4-血小板因子 4、肝素诱导的血小板减少症和癌症。

CXCL4-platelet factor 4, heparin-induced thrombocytopenia and cancer.

机构信息

Oslo University Hospital Rikshospitalet, Department of Haematology and Research Institute of Internal Medicine, and University of Oslo, Institute of Clinical Medicine, Oslo, Norway.

出版信息

Thromb Res. 2012 Apr;129 Suppl 1:S97-100. doi: 10.1016/S0049-3848(12)70026-9.

Abstract

Platelet factor 4 (CXCL4-PF4) is a chemokine that binds to and neutralizes heparin and other negatively charged proteoglycans, but is also involved in angiogenesis and cancer development. In some patients exposed to heparin, antibodies are generated against the CXCL-PF4/heparin complex that may activate platelets and coagulation and lead to thrombocytopenia and arterial or venous thrombosis, a condition commonly named heparin induced thrombocytopenia (HIT). HIT has been investigated in numerous clinical settings, but there is limited data on the epidemiology and phenotype of HIT in cancer patients. The present review describes the role of CXCL4-PF4 in cancer, the immunobiology, clinical presentation and diagnosis of HIT, and the specific problems faced in cancer patients.

摘要

血小板因子 4(CXCL4-PF4)是一种趋化因子,可与肝素和其他带负电荷的蛋白聚糖结合并中和它们,但也参与血管生成和癌症发展。在一些接触肝素的患者中,会针对 CXCL-PF4/肝素复合物产生抗体,这些抗体可能会激活血小板并引发凝血,导致血小板减少症以及动脉或静脉血栓形成,这种情况通常被命名为肝素诱导的血小板减少症(HIT)。HIT 已在许多临床环境中进行了研究,但有关癌症患者中 HIT 的流行病学和表型的数据有限。本综述描述了 CXCL4-PF4 在癌症中的作用、HIT 的免疫生物学、临床表现和诊断,以及癌症患者面临的具体问题。

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