NUAK2: an emerging acral melanoma oncogene

被引:2
|
作者
Namiki, Takeshi [1 ,2 ]
Coelho, Sergio G. [1 ]
Hearing, Vincent J. [1 ]
机构
[1] NCI, Cell Biol Lab, NIH, Bethesda, MD 20814 USA
[2] Yokohama Minato Red Cross Hosp, Dept Dermatol, Kanagawa 2310801, Japan
关键词
NUAK2; acral melanoma; migration; metastasis; oncogene; ACTIVATED PROTEIN-KINASE; COMPARATIVE GENOMIC HYBRIDIZATION; HUMAN-MALIGNANT MELANOMA; CHRONIC MYELOGENOUS LEUKEMIA; ABL TYROSINE KINASE; CHRONIC MYELOID-LEUKEMIA; TUMOR-SUPPRESSOR LKB1; METASTATIC MELANOMA; CUTANEOUS MELANOMAS; BRAF MUTATIONS;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent technological advances in cancer genomics make it possible to dissect complicated genomic aberrations of melanomas. In particular, several specific genomic aberrations including 11q13 amplification and KIT aberrations have been identified in acral melanomas. We recently identified NUAK2 at 1q32 as a promising oncogene in acral melanomas and reported its significant roles in tumorigenesis in melanoma cells using both in vitro and in vivo analyses. NUAK2 as a member of the AMPK family has several intriguing aspects both as an oncogene and as a tumor suppressor gene. Here we review genomic aberrations of melanomas focusing on acral melanomas to emphasize the possible roles of NUAK2 in tumorigenesis in general and suggest that NUAK2 has pivotal roles in acral melanomagenesis.
引用
收藏
页码:695 / 704
页数:10
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