Navarini-Meury Alexander A, Conrad Curdin
Department of Dermatology, University Hospital of Zurich, Gloriastrasse 31, 8091 Zurich, Switzerland.
Semin Cancer Biol. 2009 Apr;19(2):84-91. doi: 10.1016/j.semcancer.2008.10.012. Epub 2008 Nov 7.
Unwanted growth breeds response--in the garden as well as in the tumor microenvironment. Innate immune cells mediate the earliest responses against melanoma or its precursors. However, the actual benefit by those cellular efforts is questionable. Why can early melanoma lesions actually develop in the face of rapid innate responses, and why is neutrophil- and macrophage-attracting chemokine secretion observed in melanoma? A surprisingly similar choice of chemokine receptors and chemokines are present in both innate immune cells and melanoma. Here we focus on analogies and differences between the two. Melanoma cell clusters show active chemokine signalling, with mostly tumor growth-enhancing and leukocyte-attracting effects. However, infiltrating leukocytes have only weak tumoricidal effects. Therefore, the observed leukocyte infiltration in melanoma might be at least in part an epiphenomenon of neoplastic self-stimulation rather than a full-fledged innate anti-tumor immune response.
有害生长会引发反应——无论是在花园中还是肿瘤微环境中。先天免疫细胞介导针对黑色素瘤或其前体的最早反应。然而,这些细胞活动所带来的实际益处值得怀疑。为什么早期黑色素瘤病变在快速的先天反应面前仍能实际发展,以及为什么在黑色素瘤中会观察到吸引中性粒细胞和巨噬细胞的趋化因子分泌?先天免疫细胞和黑色素瘤中存在惊人相似的趋化因子受体和趋化因子选择。在这里,我们关注两者之间的异同。黑色素瘤细胞簇显示出活跃的趋化因子信号传导,大多具有促进肿瘤生长和吸引白细胞的作用。然而,浸润的白细胞只有微弱的杀肿瘤作用。因此,在黑色素瘤中观察到的白细胞浸润可能至少部分是肿瘤自我刺激的附带现象,而非成熟的先天抗肿瘤免疫反应。