Melanoma development and progression: a conspiracy between tumor and host

被引:131
作者
Hsu, MY
Meier, F
Herlyn, M
机构
[1] Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA
[2] Thomas Jefferson Univ Hosp, Dept Pathol & Lab Med, Philadelphia, PA 19107 USA
[3] Univ Tubingen, Dept Dermatol, Tubingen, Germany
关键词
melanocyte; keratinocyte; fibroblast; endothelial cell; cadherin; gap junction; MelCAM/MUC18/CD146; growth factor; chemokine; matrix metalloproteinase;
D O I
10.1046/j.1432-0436.2002.700906.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
While a genome-centric paradigm in human cancer development was useful for the understanding of some malignancies such as leukemias, causative molecular defects intrinsic to melanocytes have not been defined in the majority of human melanomas. Recent work, however, has shown that regulatory signals governing melanocytic cell growth and differentiation may originate from the surrounding host cells either directly through physical contact or indirectly through soluble factors and extracellular matrix molecules. In this review, we present experimental systems useful for dissecting melanoma-host interactions and highlight evidence that the tumor microenvironment contributes to the oncogenic process. Thus, melanomagenesis is not merely an act of a single outlaw but a conspiracy orchestrated by multiple partners in the neighborhood who come into play in a precise spatiotemporal order. Defining intercellular molecular dialogues in human skin promises to provide key information for the development of novel treatment strategies that target the functional unit of stroma and tumor.
引用
收藏
页码:522 / 536
页数:15
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