Zaidi M Raza, Day Chi-Ping, Merlino Glenn
Laboratory of Cancer Biology and Genetics, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-4264, USA.
J Invest Dermatol. 2008 Oct;128(10):2381-91. doi: 10.1038/jid.2008.177.
Cutaneous malignant melanoma is highly invasive and capable of metastasizing to distant sites where it is typically resistant to available therapy. While striving to prevent or eradicate melanoma, researchers have two significant advantages not shared by those working on many other cancers. The main environmental etiological agent, UV radiation, is known and melanocytic lesions are excisable for molecular analysis from most stages. Yet knowledge about how UV initiates melanoma has been insufficient to achieve prevention, and the understanding of metastatic mechanisms has been inadequate to reduce mortality. Here, we review the value of melanoma mouse models, focusing on these critical early and late stages.
皮肤恶性黑色素瘤具有高度侵袭性,能够转移至远处部位,且通常对现有治疗具有抗性。在努力预防或根除黑色素瘤的过程中,研究人员拥有两个从事许多其他癌症研究的人员所没有的显著优势。主要的环境致病因素紫外线辐射是已知的,并且黑素细胞病变在大多数阶段都可切除用于分子分析。然而,关于紫外线如何引发黑色素瘤的知识还不足以实现预防,对转移机制的理解也不足以降低死亡率。在此,我们回顾黑色素瘤小鼠模型的价值,重点关注这些关键的早期和晚期阶段。