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

Author:

Massoumi Ramin12,Kuphal Silke3,Hellerbrand Claus3,Haas Bodo4,Wild Peter5,Spruss Thilo3,Pfeifer Alexander4,Fässler Reinhard1,Bosserhoff Anja K.3

Affiliation:

1. Department of Molecular Medicine, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany

2. Cell and Experimental Pathology, Department of Laboratory Medicine CRC, Malmö University Hospital, 205 02 Malmö, Sweden

3. Institute of Pathology, Department of Internal Medicine I, Institute of Pharmacy, University Regensburg, 93053 Regensburg, Germany

4. Institute for Pharmacology and Toxicology, University of Bonn, 53113 Bonn, Germany

5. Institute of Pathology, University Hospital Zürich, 8091 Zürich, Switzerland

Abstract

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.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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