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本文引用的文献

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Citrullinated histone H3, a biomarker of neutrophil extracellular trap formation, predicts the risk of venous thromboembolism in cancer patients.瓜氨酸化组蛋白 H3,中性粒细胞胞外诱捕网形成的生物标志物,可预测癌症患者发生静脉血栓栓塞的风险。
J Thromb Haemost. 2018 Mar;16(3):508-518. doi: 10.1111/jth.13951. Epub 2018 Feb 7.
2
Human pancreatic tumors grown in mice release tissue factor-positive microvesicles that increase venous clot size.在小鼠体内生长的人类胰腺肿瘤释放组织因子阳性的微囊泡,增加静脉血栓的大小。
J Thromb Haemost. 2017 Nov;15(11):2208-2217. doi: 10.1111/jth.13809. Epub 2017 Sep 20.
3
Cancer-associated pathways and biomarkers of venous thrombosis.癌症相关的静脉血栓形成途径和生物标志物。
Blood. 2017 Sep 28;130(13):1499-1506. doi: 10.1182/blood-2017-03-743211. Epub 2017 Aug 14.
4
Tumor-Derived Exosomes Induce the Formation of Neutrophil Extracellular Traps: Implications For The Establishment of Cancer-Associated Thrombosis.肿瘤来源的外泌体诱导中性粒细胞胞外陷阱的形成:对建立癌症相关血栓的影响。
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Gynecol Oncol. 2017 Jul;146(1):146-152. doi: 10.1016/j.ygyno.2017.04.021. Epub 2017 May 10.
6
Mice with a deficiency in CLEC-2 are protected against deep vein thrombosis.CLEC-2 缺乏的小鼠对深静脉血栓形成具有抵抗力。
Blood. 2017 Apr 6;129(14):2013-2020. doi: 10.1182/blood-2016-09-742999. Epub 2017 Jan 19.
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Prostaglandin E synthase is upregulated by Gas6 during cancer-induced venous thrombosis.Gas6 在癌症诱导的静脉血栓形成过程中上调前列腺素 E 合酶。
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Tissue factor-positive tumor microvesicles activate platelets and enhance thrombosis in mice.组织因子阳性肿瘤微泡激活小鼠血小板并增强血栓形成。
J Thromb Haemost. 2016 Jan;14(1):153-66. doi: 10.1111/jth.13181. Epub 2015 Dec 11.
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癌症相关性血栓形成的小鼠模型。

Mouse models of cancer-associated thrombosis.

机构信息

Department of Medicine, Division of Hematology and Oncology, Thrombosis and Hemostasis Program, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA; K. G. Jebsen Thrombosis Research and Expertise Center, University of Tromsø, Tromsø, Norway.

Department of Medicine, Division of Hematology and Oncology, Thrombosis and Hemostasis Program, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA; Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

出版信息

Thromb Res. 2018 Apr;164 Suppl 1(Suppl 1):S48-S53. doi: 10.1016/j.thromres.2017.12.018. Epub 2017 Dec 29.

DOI:10.1016/j.thromres.2017.12.018
PMID:29306575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5942599/
Abstract

Cancer patients have an increased risk of venous thromboembolism (VTE) compared with the general population. Mouse models are used to better understand the mechanisms of cancer-associated thrombosis. Several mouse models of cancer-associated thrombosis have been developed that use different mouse strains, tumors, tumor sites and thrombosis models. In this review, we summarize these different models. These models have been used to determine the role of different pathways in cancer-associated thrombosis. For instance, they have revealed roles for tumor-derived tissue factor-positive microvesicles and neutrophil extracellular traps in thrombosis in tumor-bearing mice. A better understanding of the mechanisms of cancer-associated thrombosis may allow the development of new therapies to reduce thrombosis in cancer patients.

摘要

癌症患者发生静脉血栓栓塞症(venous thromboembolism,VTE)的风险高于普通人群。人们使用小鼠模型来更好地理解与癌症相关的血栓形成机制。目前已经开发出多种与癌症相关的血栓形成小鼠模型,这些模型使用了不同的小鼠品系、肿瘤、肿瘤部位和血栓形成模型。在这篇综述中,我们对这些不同的模型进行了总结。这些模型被用于确定不同通路在与癌症相关的血栓形成中的作用。例如,它们揭示了肿瘤来源的组织因子阳性微囊泡和中性粒细胞胞外诱捕网在荷瘤小鼠血栓形成中的作用。更好地理解与癌症相关的血栓形成机制可能会促进开发新的治疗方法,以减少癌症患者的血栓形成。