Oleksowicz L, Dutcher J P
Department of Oncology, Montefiore Medical Center Hospital, Albert Einstein College of Medicine, Bronx, New York 10467, USA.
Med Oncol. 1995 Jun;12(2):95-102. doi: 10.1007/BF01676709.
In vitro and in vivo studies have demonstrated that adhesive interactions between tumor cells and platelets may play a central role in the metastatic process. Ultrastructural studies have demonstrated that platelets appear to enhance the development of arrested tumor emboli into a secondary metastatic colony. Platelet adhesive glycoprotein receptors and their immunorelated counterparts expressed by tumor cells participate in tumor-induced platelet aggregation, which may be an early step in the development of a metastatic lesion. Platelet anti-adhesive agents have been demonstrated to reduce metastases in rodent models. Although tumor adhesive glycoproteins have yet to be fully characterized, specific inhibition of their functional sites could constitute a forthcoming strategy for effective inhibition of metastases.
体外和体内研究表明,肿瘤细胞与血小板之间的黏附相互作用可能在转移过程中起核心作用。超微结构研究表明,血小板似乎会促进停滞的肿瘤栓子发展为继发性转移瘤。肿瘤细胞表达的血小板黏附糖蛋白受体及其免疫相关对应物参与肿瘤诱导的血小板聚集,这可能是转移病灶发展的早期步骤。血小板抗黏附剂已被证明可减少啮齿动物模型中的转移。尽管肿瘤黏附糖蛋白尚未完全表征,但对其功能位点的特异性抑制可能构成有效抑制转移的未来策略。