Crissman J D
Pathol Annu. 1986;21 Pt 1:29-52.
Many of these observations appear to define a reasonable hypothesis. High-grade or poorly differentiated malignant neoplasms have a shorter tumor-doubling time, are less cohesive, often with irregular borders, and tend to invade by small aggregates and individual tumor cells. The observation of the pattern of invasion provides considerable information on the aggressiveness of the neoplasm. The pattern of invasion appears to correlate with tumor cell cohesiveness, motility, loss of contact inhibition, excretion of enzymes, and other factors associated with aggressiveness in experimental models. It is clear that the pattern of tumor-host interaction indirectly reflects many of these parameters and provides major clues to the biologic potential of human carcinomas. These observations should be used to supplement the histologic and cytologic features commonly used to derive a tumor grade. Aggressive tumors are usually larger and are associated with a greater blood supply. Vascular invasion is more common in this situation and large veins may be invaded by tumor by intravascular growth. Penetration of small lymphatic and blood vessels is associated with a poor prognosis and involvement of large veins with intravascular extensions of tumor have the potential of releasing tumor cell aggregates or emboli into the venous circulation. These large tumor cell aggregates have been demonstrated to be associated with a higher efficiency of metastasis formation and infer a poorer prognosis. Why have I bothered with all this detail about the occurrence of circulating tumor cells and their relation to the development of metastases? It must be stressed that many malignant cells are being released into the circulation of cancer patients and few, if any, ever successfully complete the complex sequence leading to a metastatic focus. This has been termed "metastatic inefficiency." Other investigators have referred to the unique cells that have mastered the intricate sequence of steps required to establish metastases as winners of the metastases decathlon. The observations of vascular (lymphatic or blood) invasion in random tissue sections and their relation to patient prognosis can be best explained by our basic knowledge of cancer biology. The finding of occasional small aggregates of single tumor cells in vascular spaces statistically implies that a considerable number of cells must be entering the vascular compartment.(ABSTRACT TRUNCATED AT 400 WORDS)
这些观察结果中的许多似乎都能界定一个合理的假说。高级别或低分化恶性肿瘤的肿瘤倍增时间较短,细胞间黏附性较差,边界常不规则,且倾向于以小细胞团和单个肿瘤细胞的形式浸润。对浸润模式的观察为肿瘤的侵袭性提供了大量信息。浸润模式似乎与肿瘤细胞的黏附性、运动性、接触抑制的丧失、酶的分泌以及实验模型中与侵袭性相关的其他因素有关。显然,肿瘤与宿主的相互作用模式间接反映了其中许多参数,并为人类癌症的生物学潜能提供了重要线索。这些观察结果应用于补充通常用于确定肿瘤分级的组织学和细胞学特征。侵袭性强的肿瘤通常更大,且血供更丰富。在这种情况下,血管侵犯更为常见,大静脉可能会被肿瘤通过血管内生长方式侵犯。小淋巴管和血管的穿透与预后不良相关,而肿瘤血管内扩展累及大静脉则有可能将肿瘤细胞团或栓子释放到静脉循环中。这些大的肿瘤细胞团已被证明与转移形成的更高效率相关,并预示着更差的预后。我为何要详述循环肿瘤细胞的发生及其与转移发展的关系呢?必须强调的是,许多恶性细胞正在释放到癌症患者的循环系统中,但很少有细胞(如果有的话)能成功完成导致转移灶形成的复杂过程。这被称为“转移低效性”。其他研究者将那些成功完成建立转移所需复杂步骤序列的独特细胞称为转移十项全能的获胜者。在随机组织切片中观察到的血管(淋巴管或血管)侵犯及其与患者预后的关系,可通过我们对癌症生物学的基础知识得到最佳解释。在血管腔内偶尔发现单个肿瘤细胞的小细胞团,从统计学角度意味着必然有相当数量的细胞进入了血管腔室。(摘要截选至400字)