Down-regulation of CYLD expression by Snail promotes tumor progression in malignant melanoma

被引:183
|
作者
Massoumi, Ramin [1 ,6 ]
Kuphal, Silke [2 ]
Hellerbrand, Claus [3 ]
Haas, Bodo [5 ]
Wild, Peter [7 ]
Spruss, Thilo [4 ]
Pfeifer, Alexander [5 ]
Faessler, Reinhard [1 ]
Bosserhoff, Anja K. [2 ]
机构
[1] Max Planck Inst Biochem, Dept Mol Med, D-82152 Martinsried, Germany
[2] Univ Regensburg, Inst Pathol, D-93053 Regensburg, Germany
[3] Univ Regensburg, Dept Internal Med 1, D-93053 Regensburg, Germany
[4] Univ Regensburg, Inst Pharm, D-93053 Regensburg, Germany
[5] Univ Bonn, Inst Pharmacol & Toxicol, D-53113 Bonn, Germany
[6] Malmo Univ Hosp, Dept Lab Med CRC, S-20502 Malmo, Sweden
[7] Univ Zurich Hosp, Inst Pathol, CH-8091 Zurich, Switzerland
来源
JOURNAL OF EXPERIMENTAL MEDICINE | 2009年 / 206卷 / 01期
关键词
NF-KAPPA-B; EPITHELIAL-MESENCHYMAL TRANSITIONS; E-CADHERIN EXPRESSION; TRANSCRIPTION FACTOR SNAIL; INHIBITING ACTIVITY; SIGNALING PATHWAY; UP-REGULATION; HUMAN COLON; CELLS; MIGRATION;
D O I
10.1084/jem.20082044
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
High malignancy and early metastasis are hallmarks of melanoma. Here, we report that the transcription factor Snail1 inhibits expression of the tumor suppressor CYLD in melanoma. As a direct consequence of CYLD repression, the protooncogene BCL-3 translocates into the nucleus and activates Cyclin D1 and N-cadherin promoters, resulting in proliferation and invasion of melanoma cells. Rescue of CYLD expression in melanoma cells reduced proliferation and invasion in vitro and tumor growth and metastasis in vivo. Analysis of a tissue microarray with primary melanomas from patients revealed an inverse correlation of Snail1 induction and loss of CYLD expression. Importantly, tumor thickness and progression-free and overall survival inversely correlated with CYLD expression. Our data suggest that Snail1-mediated suppression of CYLD plays a key role in melanoma malignancy.
引用
收藏
页码:221 / 232
页数:12
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