Department of Dermatology, Eberhard Karls University, Tübingen, Germany.
J Clin Invest. 2010 Jun;120(6):1800-3. doi: 10.1172/JCI43424. Epub 2010 May 24.
The classical model of metastasis is that tumor cell dissemination occurs late in tumor development, after the primary tumor has grown, and that only then will tumor cells invade the local tissue, enter the blood or lymphatic vessels, and colonize new sites to cause metastases. However, evidence increasingly indicates that single tumor cells spread to distant sites much earlier than previously believed. In this issue of the JCI, Eyles and colleagues provide new insight into the mechanisms underlying early tumor cell dissemination, formation of metastases, and tumor immunosurveillance using transgenic mice that spontaneously develop melanomas of the uvea. The authors provide striking evidence that tumor cells start to disseminate during the initial steps of tumor development, that late appearing metastases arise from these early disseminated tumor cells, and that CD8+ T cells inhibit the growth of disseminated tumor cells, surprisingly, not by cytotoxic effects, but through cytostatic effects.
经典的转移模型认为,肿瘤细胞的扩散发生在肿瘤发展的晚期,即在原发肿瘤生长之后,只有在这个时候,肿瘤细胞才会侵犯局部组织,进入血液或淋巴管,并在新的部位定植,从而导致转移。然而,越来越多的证据表明,单个肿瘤细胞的扩散发生得远比以前认为的要早。在本期 JCI 中,Eyles 及其同事使用自发性发生葡萄膜黑色素瘤的转基因小鼠,为早期肿瘤细胞扩散、转移形成和肿瘤免疫监视的机制提供了新的见解。作者提供了令人震惊的证据,表明肿瘤细胞在肿瘤发展的最初阶段就开始扩散,晚期出现的转移瘤来源于这些早期扩散的肿瘤细胞,而且 CD8+T 细胞抑制了扩散的肿瘤细胞的生长,令人惊讶的是,这种抑制作用不是通过细胞毒性作用,而是通过细胞静止作用。