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血小板聚集抑制剂对小鼠(3LL)转移形成的影响。

The influence of platelet aggregation inhibitors on metastasis formation in mice (3LL).

作者信息

Hilgard P, Heller H, Schmidt C G

出版信息

Z Krebsforsch Klin Onkol Cancer Res Clin Oncol. 1976 Aug 30;86(3):243-50. doi: 10.1007/BF00286943.

Abstract

Platelets were suggested to play a specific role in the haematogenous spread of experimental tumours. To test this hypothesis mice were treated with various inhibitors or platelet function (acetyl-salicylic acid, RA 233, bencyclan-, cyproheptadine). The effect of treatment on the development of lung colonies after i.v. tumour cell injection as well as on the formation of spontaneous metastases from the solid Lewis-lung carcinoma was evaluated. A significant increase of lung colonies after pretreatment with the platelet aggregation inhibitors was found. The effect of long term treatment on spontaneous metastasis formation gave equivocal results. The present investigations do not support the importance of the integrity of platelet function as a prerequisite for metastasis formation.

摘要

血小板被认为在实验性肿瘤的血源性扩散中起特定作用。为了验证这一假设,用各种血小板功能抑制剂(乙酰水杨酸、RA 233、苄环烷、赛庚啶)对小鼠进行治疗。评估了治疗对静脉注射肿瘤细胞后肺集落形成的影响以及对实体Lewis肺癌自发转移形成的影响。发现用血小板聚集抑制剂预处理后肺集落显著增加。长期治疗对自发转移形成的影响结果不明确。目前的研究不支持血小板功能完整性作为转移形成前提条件的重要性。

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