A Re-evaluation of the "Oncogenic" Nature of Wnt/β-catenin Signaling in Melanoma and Other Cancers

被引:111
|
作者
Lucero, Olivia M. [1 ]
Dawson, David W. [2 ]
Moon, Randall T. [3 ]
Chien, Andy J. [1 ,3 ]
机构
[1] Univ Washington, Dept Med, Div Dermatol, Seattle, WA 98109 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
[3] Univ Washington, Inst Stem Cell & Regenerat Med, Seattle, WA 98109 USA
关键词
Wnt; Oncogene; Melanoma; Beta-catenin; Homeostasis; BETA-CATENIN; CELL FATE; EXPRESSION; WNT; PROGRESSION; DISEASE; REGENERATION; MELANOCYTES; INHIBITION; INCREASES;
D O I
10.1007/s11912-010-0114-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In cancer, Wnt/beta-catenin signaling is ubiquitously referred to as an "oncogenic" pathway that promotes tumor progression. This review examines how the regulation and downstream effects of Wnt/beta-catenin signaling in cancer varies depending on cellular context, with a focus on malignant melanoma. We emphasize that the cellular homeostasis of Wnt/beta-catenin signaling may represent a more appropriate concept than the simplified view of the Wnt/beta-catenin pathway as either oncogenic or tumor-suppressing. Ultimately, a more refined understanding of the contextual regulation of Wnt/beta-catenin signaling will be essential for addressing if and how therapeutic targeting of this pathway could be leveraged for patient benefit.
引用
收藏
页码:314 / 318
页数:5
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