Pro-Invasive Activity of the Hippo Pathway Effectors YAP and TAZ in Cutaneous Melanoma

• Published in: Journal of investigative dermatology Vol. 134; no. 1; pp. 123 - 132
• Main Authors: Nallet-Staub, Flore, Marsaud, Véronique, Li, Ling, Gilbert, Cristèle, Dodier, Sophie, Bataille, Véronique, Sudol, Marius, Herlyn, Meenhard, Mauviel, Alain
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.01.2014; Elsevier Limited; Nature Publishing Group
• Subjects: Adaptor Proteins, Signal Transducing - genetics; Adaptor Proteins, Signal Transducing - metabolism; Animals; Cell Line, Tumor; Disease Models, Animal; Female; Gene Knockdown Techniques; Humans; Lung Neoplasms - metabolism; Lung Neoplasms - secondary; Melanoma - metabolism; Melanoma - pathology; Mice; Mice, Nude; Neoplasm Invasiveness; Neoplasm Transplantation; Original; Phosphoproteins - genetics; Phosphoproteins - metabolism; Protein-Serine-Threonine Kinases - metabolism; Signal Transduction - physiology; Skin Neoplasms - metabolism; Skin Neoplasms - pathology; Transcription Factors - genetics; Transcription Factors - metabolism
• ISSN: 0022-202X; 1523-1747
• DOI: 10.1038/jid.2013.319

YAP and its paralog protein TAZ are downstream effectors of the Hippo pathway. Both are amplified in many human cancers and promote cell proliferation and epithelial–mesenchymal transition. Little is known about the status of the Hippo pathway in cutaneous melanoma. We profiled Hippo pathway component expression in a panel of human melanoma cell lines and melanocytic lesions, and characterized the capacity of YAP and TAZ to control melanoma cell behavior. YAP and TAZ immuno-staining in human samples revealed mixed cytoplasmic and nuclear staining for both proteins in benign nevi and superficial spreading melanoma. TAZ was expressed at higher levels than YAP1/2 in all cell lines and in those with high invasive potential. Stable YAP or TAZ knockdown dramatically reduced the expression of the classical Hippo target CCN2/connective-tissue growth factor (CTGF), as well as anchorage-independent growth, capacity to invade Matrigel, and ability form lung metastases in mice following tail-vein injection. YAP knockdown also reduced invasion in a model of skin reconstruct. Inversely, YAP overexpression increased melanoma cell invasiveness, associated with increased TEA domain–dependent transcription and CCN2/CTGF expression. Together, these results demonstrate that both YAP and TAZ contribute to the invasive and metastatic capacity of melanoma cells and may represent worthy targets for therapeutic intervention.