Massoumi Ramin, Kuphal Silke, Hellerbrand Claus, Haas Bodo, Wild Peter, Spruss Thilo, Pfeifer Alexander, Fässler Reinhard, Bosserhoff Anja K
Department of Molecular Medicine, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.
J Exp Med. 2009 Jan 16;206(1):221-32. doi: 10.1084/jem.20082044. Epub 2009 Jan 5.
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.
高恶性和早期转移是黑色素瘤的特征。在此,我们报告转录因子Snail1抑制黑色素瘤中肿瘤抑制因子CYLD的表达。作为CYLD抑制的直接后果,原癌基因BCL-3易位至细胞核并激活细胞周期蛋白D1和N-钙黏蛋白启动子,导致黑色素瘤细胞增殖和侵袭。恢复黑色素瘤细胞中CYLD的表达可降低其体外增殖和侵袭能力以及体内肿瘤生长和转移能力。对来自患者的原发性黑色素瘤组织芯片分析显示,Snail1诱导与CYLD表达缺失呈负相关。重要的是,肿瘤厚度、无进展生存期和总生存期与CYLD表达呈负相关。我们的数据表明,Snail1介导的CYLD抑制在黑色素瘤恶性进展中起关键作用。