Warren B A
Z Krebsforsch Klin Onkol Cancer Res Clin Oncol. 1976 Sep 24;87(1):1-15. doi: 10.1007/BF00285068.
The ultrastructural morphology of the tumour cycle which has as one of its features the blood-borne tumour embolus associated with thrombosis is illustrated by examples of four phases. (1) The intrinsic vasculature of tumours influences the process of intravasation of tumour cells to form bloodborne emboli. Scanning electron microscopy of melanoma tumours reveals channels containing erythrocytes which are sinusoidal in appearance. (2) The reaction of the circulating blood to the villi and folds of tumour cells is to coat the surface with plasma proteins and platelets. Walker 256 carcinoma cells become encrusted with platelets following agitation with rat platelet rich plasma. (3) Damaged endothelium appears to provide a more secure adhesional site for the tumour embolus. Platelets on a damaged site may provide an active adhesional region for the platelets on the passing embolus. (4) Tumour cells migrate through the endothelial layer from the adherent embolus and can be held up at the level of the basement membrane of the endothelium.
肿瘤循环的超微结构形态以血行肿瘤栓子伴血栓形成作为其特征之一,通过四个阶段的实例进行说明。(1)肿瘤的固有血管系统影响肿瘤细胞进入血管形成血行栓子的过程。黑色素瘤肿瘤的扫描电子显微镜检查显示含有红细胞的通道,其外观呈窦状。(2)循环血液对肿瘤细胞的绒毛和褶皱的反应是用血浆蛋白和血小板覆盖其表面。沃克256癌细胞与富含大鼠血小板的血浆搅拌后会被血小板覆盖。(3)受损的内皮似乎为肿瘤栓子提供了更牢固的粘附位点。受损部位的血小板可能为通过的栓子上的血小板提供一个活跃的粘附区域。(4)肿瘤细胞从粘附的栓子穿过内皮细胞层,并可在内皮基底膜水平处停滞。