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      Restoration of caveolin-1 expression suppresses growth and metastasis of head and neck squamous cell carcinoma

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          Abstract

          Caveolin-1 (Cav-1) plays an important role in modulating cellular signalling, but its role in metastasis is not well defined. A significant reduction in Cav-1 levels was detected in lymph node metastases as compared with primary tumour of head and neck squamous cell carcinoma (HNSCC) specimens ( P<0.0001), confirming the downregulation of Cav-1 observed in a highly metastatic M4 cell lines derived from our orthotopic xenograft model. To investigate the function of Cav-1 in metastasis of HNSCC, we compared stable clones of M4 cells carrying human cav-1 cDNA (CavS) with cells expressing an empty vector (EV) in vitro and in the orthotopic xenograft model. Overexpression of Cav-1 suppressed growth of the CavS tumours compared with the EV tumours. The incidence of lung metastases was significantly lower in animals carrying CavS tumours than those with EV tumours ( P=0.03). In vitro, CavS cells displayed reduced cell growth, invasion, and increased anoikis compared with EV cells. In CavS cells, Cav-1 formed complex with integrin β1 and Src. Further application of integrin β1 neutralising antibody or Src inhibitor PP2 to EV cells illustrated similar phenotypes as CavS cells, suggesting that Cav-1 may play an inhibitory role in tumorigenesis and lung metastasis through regulating integrin β1- and Src-mediated cell–cell and cell–matrix interactions.

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          Most cited references27

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          A renaissance for SRC.

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            Caveolin-1 in oncogenic transformation, cancer, and metastasis.

            Caveolae are 50- to 100-nm omega-shaped invaginations of the plasma membrane that function as regulators of signal transduction. Caveolins are a class of oligomeric structural proteins that are both necessary and sufficient for caveolae formation. Interestingly, caveolin-1 has been implicated in the pathogenesis of oncogenic cell transformation, tumorigenesis, and metastasis. Here, we review the available experimental evidence (gleaned from cultured cells, animal models, and human tumor samples) that caveolin-1 (Cav-1) functions as a "tumor and/or metastasis modifier gene." Genetic evidence from the study of Cav-1(-/-) null mice and human breast cancer mutations [CAV-1 (P132L)] supports the idea that caveolin-1 normally functions as a negative regulator of cell transformation and mammary tumorigenesis. In contrast, caveolin-1 may function as a tumor promoter in prostate cancers. We discuss possible molecular mechanisms to explain these intriguing, seemingly opposing, findings. More specifically, caveolin-1 phosphorylation (at Tyr14 and Ser80) and mutations (P132L) may override or inactivate the growth inhibitory activity of the caveolin-scaffolding domain (residues 82-101).
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              A requirement for caveolin-1 and associated kinase Fyn in integrin signaling and anchorage-dependent cell growth.

              Caveolin-1 functions as a membrane adaptor to link the integrin alpha subunit to the tyrosine kinase Fyn. Upon integrin ligation, Fyn is activated and binds, via its SH3 domain, to Shc. Shc is subsequently phosphorylated at tyrosine 317 and recruits Grb2. This sequence of events is necessary to couple integrins to the Ras-ERK pathway and promote cell cycle progression. These findings reveal an unexpected function of caveolin-1 and Fyn in integrin signaling and anchorage-dependent cell growth.
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                Author and article information

                Journal
                Br J Cancer
                British Journal of Cancer
                Nature Publishing Group
                0007-0920
                1532-1827
                28 October 2008
                11 November 2008
                04 November 2008
                : 99
                : 10
                : 1684-1694
                Affiliations
                [1 ]Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine Atlanta, GA, USA
                [2 ]Department of Pathology, Emory University School of Medicine Atlanta, GA, USA
                [3 ]Department of Biostatistics and Bioinformatics, Emory University Rollins School of Public Health Atlanta, GA, USA
                [4 ]Quest Diagnostics Atlanta, GA, USA
                [5 ]Department of Anatomic Pathology, The Cleveland Clinic Cleveland, OH, USA
                Author notes
                [* ]Author for correspondence: gzchen@ 123456emory.edu
                Article
                6604735
                10.1038/sj.bjc.6604735
                2584955
                19002186
                7ed61ce0-e1a8-41c9-9c94-9ee064add83a
                Copyright 2008, Cancer Research UK
                History
                : 03 June 2008
                : 01 September 2008
                : 23 September 2008
                Categories
                Molecular Diagnostics

                Oncology & Radiotherapy
                caveolin-1,integrin β1,squamous cell carcinoma of the head and neck,src

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