Lejeune Ferdy J, Rimoldi Donata, Speiser Daniel
Ludwig Institute for Cancer Research, Division of Clinical Onco-Immunology and Centre Hospitalier Universitaire Vaudois, Department of Visceral Surgery, Lausanne, Switzerland.
Expert Rev Anticancer Ther. 2007 May;7(5):701-13. doi: 10.1586/14737140.7.5.701.
Classical metastatic melanoma therapy is disappointing but important progress has been made in the understanding of melanoma biology. Genetic lesions and several intracellular signaling pathways that could serve as targets for novel therapy have been identified and a number of new agents are under evaluation. Promising tumor cell targets were identified in the cell membrane, cytoplasm and nucleus. New therapeutic approaches, besides monoclonal antibodies and vaccination, include an increasing number of small molecules that have been shown to interfere restrictively with intracellular signaling pathways in melanoma and decrease proliferation, survival, migration or invasion. Other agents can interfere with stromal components of melanoma, such as angiogenesis and components of the immune system.
经典的转移性黑色素瘤治疗效果令人失望,但在黑色素瘤生物学的理解方面已取得重要进展。已确定了可作为新型治疗靶点的基因损伤和几种细胞内信号通路,并且一些新药物正在评估中。在细胞膜、细胞质和细胞核中确定了有前景的肿瘤细胞靶点。除单克隆抗体和疫苗接种外,新的治疗方法还包括越来越多的小分子,这些小分子已被证明可限制性地干扰黑色素瘤的细胞内信号通路,并减少增殖、存活、迁移或侵袭。其他药物可干扰黑色素瘤的基质成分,如血管生成和免疫系统成分。