Tsubura E, Yamashita T, Sone S
Cancer Metastasis Rev. 1983;2(3):223-37. doi: 10.1007/BF00048479.
Most metastases in patients occur as a result of hematogenous dissemination of tumor cells. This process of metastasis is complex and consists of several steps, foremost of which is the arrest of circulating emboli in capillary beds and the formation of a thrombus at that site. Thrombus formation in the metastasis of human cancer was described first by Billroth in 1878. It was reported that the organization of tumor cell emboli, and the subsequent penetration of tumor cells into the capillary wall, was the first stage of metastasis. Since then, many investigations and observations have been made clinically as well as experimentally to clarify the process (or mechanisms) of tumor cell arrest and how to inhibit it. Coagulative and fibrinolytic pathways were believed to have a main role in thrombus formation. However, other factors responsible for the relationship between tumor cells and the host must be also considered. Elegant and extensive studies by Fidler and Kripke demonstrated that development of metastasis is not a random process, but a selection process of specialized subpopulations of highly metastatic cells within the primary tumors. Biochemical constituents and ionic properties on cell surfaces, deformability or locomotive activities of tumor cells, as well as thrombo-plastic-fibrinolytic activities, are also important factors determining the arrest patterns of circulating tumor cells. On the other hand, host defense factors against tumor cells in the bloodstream have been attracting much attention recently in tumor immunology. Host defense factors relating the arrest of tumor cells to the establishment of metastatic foci seemed difficult to define, since many studies showed contradictory data concerning the influence of immune response on tumor cell arrest. Hemodynamic abnormality may also influence the arrest of tumor cells in the circulation. Hypercoagulability induced from host tissues is greatly associated with the arrest patterns. Platelet activities might affect thrombus formation. Nevertheless, exact explanations of the process or mechanisms inhibiting or enhancing the arrest of tumor cells after hematogenous dissemination have not been obtained. In any event, for cancer treatment, it is important to determine which substances inhibit the arrest of circulating tumor cells and how to prevent hematogenous metastasis. In this review, we will focus upon coagulative and fibrinolytic processes and then upon substances that inhibit the arrest of circulating tumor cells. Furthermore, some comments on the possible clinical applications of inhibitory substances for prevention of cancer metastasis are added.
大多数患者的转移是肿瘤细胞经血行播散所致。这种转移过程很复杂,由几个步骤组成,其中首要的是循环栓子在毛细血管床中滞留并在该部位形成血栓。1878年,比尔罗特首次描述了人类癌症转移中的血栓形成。据报道,肿瘤细胞栓子的机化以及随后肿瘤细胞穿透毛细血管壁是转移的第一阶段。从那时起,人们在临床和实验上进行了许多研究和观察,以阐明肿瘤细胞滞留的过程(或机制)以及如何抑制它。凝血和纤溶途径被认为在血栓形成中起主要作用。然而,还必须考虑其他与肿瘤细胞和宿主之间关系有关的因素。菲德勒和克里普克进行的精细而广泛的研究表明,转移的发生不是一个随机过程,而是原发性肿瘤内高转移性细胞的特殊亚群的选择过程。细胞表面的生化成分和离子特性、肿瘤细胞的可变形性或运动活性,以及血栓形成 - 纤维蛋白溶解活性,也是决定循环肿瘤细胞滞留模式的重要因素。另一方面,血液中宿主针对肿瘤细胞的防御因子最近在肿瘤免疫学中备受关注。由于许多研究显示免疫反应对肿瘤细胞滞留的影响的数据相互矛盾,因此将肿瘤细胞滞留与转移灶形成相关的宿主防御因子似乎难以界定。血流动力学异常也可能影响循环中肿瘤细胞的滞留。宿主组织诱导的高凝状态与滞留模式密切相关。血小板活性可能影响血栓形成。然而,对于血行播散后抑制或增强肿瘤细胞滞留的过程或机制尚未得到确切解释。无论如何,对于癌症治疗而言,确定哪些物质抑制循环肿瘤细胞的滞留以及如何预防血行转移很重要。在本综述中,我们将重点关注凝血和纤溶过程,然后关注抑制循环肿瘤细胞滞留的物质。此外,还增加了一些关于抑制物质预防癌症转移的可能临床应用的评论。