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肝素的转移增强作用及其与一种脂蛋白因子的关系。

Metastasis-enhancing effect of heparin and its relationship to a lipoprotein factor.

作者信息

Chan S Y, Pollard M

出版信息

J Natl Cancer Inst. 1980 May;64(5):1121-5.

PMID:6929014
Abstract

The effect of low-dose heparin on spontaneous metastasis formation was studied with the PA-III rat prostate adenocarcinoma cell line model system. In LW rats given heparin iv at a dose of 1,000 U/kg body weight (three times/wk), the metastatic spread of implanted PA-III cells from the footpad through ipsilateral lymphatics to the lungs was enhanced. The weights of the draining lymph nodes (popliteal, inguinal, and axillary) and the number of lung tumor colonies were significantly increased compared with those in the saline-treated control tumor-bearing rats. The growth of the primary tumor was also enhanced. Heparin alone did not induce enlarged lymph nodes in rats nor did it change the growth pattern of PA-III cells in vitro. The accelerated metastatic spread of the PA-III cells was possibly related to the destruction of the oncolytic activity of the very low-density lipoprotein by the lipoprotein lipases induced by the iv administration of heparin. However, the possibility that other mechanisms could be operative in this phenomenon has not been ruled out.

摘要

采用PA - III大鼠前列腺腺癌细胞系模型系统研究了低剂量肝素对自发转移形成的影响。在以1000 U/kg体重的剂量静脉注射肝素(每周三次)的LW大鼠中,植入的PA - III细胞从足垫经同侧淋巴管向肺部的转移扩散增强。与生理盐水处理的对照荷瘤大鼠相比,引流淋巴结(腘窝、腹股沟和腋窝)的重量和肺肿瘤集落数显著增加。原发肿瘤的生长也增强。单独使用肝素不会导致大鼠淋巴结肿大,也不会改变PA - III细胞在体外的生长模式。PA - III细胞转移扩散加速可能与静脉注射肝素诱导的脂蛋白脂肪酶破坏极低密度脂蛋白的溶瘤活性有关。然而,尚未排除其他机制在这一现象中起作用的可能性。

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