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    Targeting the Hippo Signaling Pathway in Atypical Teratoid Rhabdoid Tumor

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    Author
    Norris, Gregory
    Affiliation
    The University of Arizona College of Medicine - Phoenix
    Issue Date
    2017-05-26
    Keywords
    Cancer
    Pediatric
    Brain Tumor
    Atypical Teratoid Rhabdoid Tumor
    Hippo Signaling Pathway
    Verteporfin
    MeSH Subjects
    Brain Neoplasms
    Child
    Polymerase Chain Reaction
    Sequence Analysis, RNA
    Dose-Response Relationship, Drug
    Gene Expression
    Treatment Outcome
    
    Metadata
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    Publisher
    The University of Arizona.
    Description
    A Thesis submitted to The University of Arizona College of Medicine - Phoenix in partial fulfillment of the requirements for the Degree of Doctor of Medicine.
    URI
    http://hdl.handle.net/10150/623631
    Abstract
    Atypical teratoid rhabdoid tumor (ATRT) is a highly malignant pediatric central nervous system tumor. The prognosis is often poor, with a 2‐year survival rate estimated at 15%. This dismal prognosis highlights the need to develop new treatment modalities for this devastating pediatric tumor. Recently, a tumor suppressing signaling pathway known as Hippo has emerged as a possible cancer treatment target. The Hippo signaling pathway is involved in organ growth and maintenance, and is dysregulated in many diverse cancers. We used quantitative real‐time PCR to evaluate the mRNA expression profile of Hippo pathway genes. We then used determined the protein expression of various Hippo components using Western blots. The results of this study suggest that Hippo plays a definite role in atypical teratoid rhabdoid tumor.
    Type
    text; Electronic Thesis
    Language
    en_US
    Collections
    College of Medicine - Phoenix, Scholarly Projects

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