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Transforming Growth Factor-{beta}1 Promotes Matrix Metalloproteinase-9-Mediated Oral Cancer Invasion through Snail Expression.

Transforming Growth Factor-{beta}1 Promotes Matrix Metalloproteinase-9-Mediated Oral Cancer Invasion through Snail Expression. Research Abstract Details 

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  • Transforming Growth Factor-{beta}1 Promotes Matrix Metalloproteinase-9-Mediated Oral Cancer Invasion through Snail Expression. Abstract Text:

    limin sunLimin Sun,michelle e diamondMichelle E Diamond,adam j ottavianoAdam J Ottaviano,mathew j josephMathew J Joseph,vijayalakshmi ananthanarayanVijayalakshmi Ananthanarayan,hidayatullah g munshiHidayatullah G Munshi,limin sunLimin Sun,michelle e diamondMichelle E Diamond,adam j ottavianoAdam J Ottaviano,mathew j josephMathew J Joseph,vijayalakshmi ananthanarayanVijayalakshmi Ananthanarayan,hidayatullah g munshiHidayatullah G Munshi,

    Oral squamous cell carcinoma (OSCC), which is the most common malignancy of the oral cavity, is often associated with local and regional invasion. Increased expression of matrix metalloproteinase-9 (MMP-9) is correlated with invasive behavior of OSCC. Because transforming growth factor beta1 (TGF-beta1) is up-regulated in OSCC tumors, we examined the relationship between TGF-beta1 signaling and MMP-9 in human OSCC specimens. Evaluation of human specimens showed that tumors with enhanced TGF-beta1 signaling also showed increased MMP-9 expression. Because the transcription factor Snail has been determined to be a key mediator of TGF-beta1 signaling, we evaluated the role of Snail in TGF-beta1-mediated MMP-9 expression. Initially, we examined the extent to which TGF-beta1 regulated Snail expression in oral keratinocytes and in OSCC cell lines. TGF-beta1 enhanced Snail expression in a majority of the cell lines examined, with the largest induction of Snail detected in UMSCC1 cells. Interestingly, overexpression of Snail in UMSCC1 cells enhanced MMP-9 and tissue inhibitor of metalloproteinase-1 protein levels. Despite the increase in the tissue inhibitor of metalloproteinase-1 protein, there was a net increase in the pericellular proteolytic activity as shown by enhanced MMP-9-dependent Matrigel invasion. Moreover, Snail-specific siRNA blocked TGF-beta1-induced MMP-9 expression and Matrigel invasion. In addition, Snail increased Ets-1 levels and Ets-1-specific siRNA blocked both Snail- and TGF-beta1-mediated MMP-9 expression and Matrigel invasion. Thus, these data show that Snail functions as a molecular mediator of TGF-beta1-regulated MMP-9 expression by increasing Ets-1 and thereby contributing to oral cancer progression. (Mol Cancer Res 2008;6(1):10-20).

    Transforming Growth Factor-{beta}1 Promotes Matrix Metalloproteinase-9-Mediated Oral Cancer Invasion through Snail Expression. Publishing Authors By Initials

    l sunL Sun,me diamondME Diamond,aj ottavianoAJ Ottaviano,mj josephMJ Joseph,v ananthanarayanV Ananthanarayan,hg munshiHG Munshi,l sunL Sun,me diamondME Diamond,aj ottavianoAJ Ottaviano,mj josephMJ Joseph,v ananthanarayanV Ananthanarayan,hg munshiHG Munshi,

    For similar abstracts research abstracts see: abstracts research

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    Transforming Growth Factor-{beta}1 Promotes Matrix Metalloproteinase-9-Mediated Oral Cancer Invasion through Snail Expression. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Molecular cancer research : MCR

    VOLUME: 6

    Page Numbers: 10-20

    Journal Abbreviation: Mol. Cancer Res.

    ISSN: 1541-7786

    DAY: 31

    MONTH: Jan

    YEAR: 2008

    Transforming Growth Factor-{beta}1 Promotes Matrix Metalloproteinase-9-Mediated Oral Cancer Invasion through Snail Expression. Information

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    LANGUAGE: eng

    NlmUniqueID: 101150042

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    Grant and Affiliation Information for Transforming Growth Factor-{beta}1 Promotes Matrix Metalloproteinase-9-Mediated Oral Cancer Invasion through Snail Expression.

    AFFILIATION: Department of Medicine, Northwestern University Medical School, 303 East Superior Avenue, Lurie 3-117, Chicago, IL 60611. h-munshi@northwestern.edu.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Mol Cancer Res

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