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Early tumor dissemination, but late metastasis: insights into tumor dormancy

机译:肿瘤早期传播,但晚期转移:洞悉肿瘤的潜伏期

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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.
机译:转移的经典模型是,肿瘤细胞的扩散发生在原发肿瘤生长后的肿瘤发展的后期,只有这样,肿瘤细胞才会侵入局部组织,进入血液或淋巴管,并在新的位点定居以引起转移。然而,越来越多的证据表明,单个肿瘤细胞比以前认为的更早扩散到远处。在本期JCI中,Eyles及其同事使用自发形成葡萄膜黑色素瘤的转基因小鼠,对早期肿瘤细胞扩散,转移的形成和肿瘤免疫监测的潜在机制提供了新的见解。作者提供了惊人的证据,即肿瘤细胞在肿瘤发展的初始阶段开始扩散,这些早期扩散的肿瘤细胞开始出现晚期转移,而CD8〜(+)T细胞抑制了扩散的肿瘤细胞的生长,令人惊讶的是,不是通过细胞毒性作用,而是通过细胞抑制作用。

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