MicroRNA miR-196a is a central regulator of HOX-B7 and BMP4 expression in malignant melanoma

被引:113
作者
Braig, Simone [1 ]
Mueller, Daniel W. [1 ]
Rothhammer, Tanja [1 ]
Bosserhoff, Anja-Katrin [1 ]
机构
[1] Univ Regensburg, Sch Med, Inst Pathol, D-93053 Regensburg, Germany
关键词
Malignant melanoma; Bone morphogenetic proteins; MicroRNA; HOX genes; Fibroblast growth factor; Migration; BONE MORPHOGENETIC PROTEINS; FIBROBLAST-GROWTH-FACTOR; MESSENGER-RNA; TUMOR-GROWTH; IN-VITRO; PROMOTES PROGRESSION; CELL-PROLIFERATION; OVARIAN-CANCER; BREAST-CANCER; INVASION;
D O I
10.1007/s00018-010-0394-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Since bone morphogenetic proteins (BMPs) play an important role in melanoma progression, we aimed to determine the molecular mechanisms leading to overexpression of BMP4 in melanoma cells compared to normal melanocytes. With our experimental approach we revealed that loss of expression of a microRNA represents the starting point for a signaling cascade finally resulting in overexpression of BMP4 in melanoma cells. In detail, strongly reduced expression of the microRNA miR-196a in melanoma cells compared to healthy melanocytes leads to enhanced HOX-B7 mRNA and protein levels, which subsequently raise Ets-1 activity by inducing basic fibroblast growth factor (bFGF). Ets-1 finally accounts for induction of BMP4 expression. We were furthermore able to demonstrate that bFGF-mediated induction of migration is achieved via activation of BMP4, thus determining BMP4 as major modulator of migration in melanoma. In summary, our study provides insights into the early steps of melanoma progression and might thereby harbor therapeutic relevance.
引用
收藏
页码:3535 / 3548
页数:14
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