| MDM2, MDMX and p53 in oncogenesis and cancer therapy. | |
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MedLine Citation:
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PMID: 23303139 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
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The MDM2 and MDMX (also known as HDMX and MDM4) proteins are deregulated in many human cancers and exert their oncogenic activity predominantly by inhibiting the p53 tumour suppressor. However, the MDM proteins modulate and respond to many other signalling networks in which they are embedded. Recent mechanistic studies and animal models have demonstrated how functional interactions in these networks are crucial for maintaining normal tissue homeostasis, and for determining responses to oncogenic and therapeutic challenges. This Review highlights the progress made and pitfalls encountered as the field continues to search for MDM-targeted antitumour agents. |
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Authors:
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Mark Wade; Yao-Cheng Li; Geoffrey M Wahl |
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Publication Detail:
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Type: JOURNAL ARTICLE Date: 2013-1-10 |
Journal Detail:
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Title: Nature reviews. Cancer Volume: - ISSN: 1474-1768 ISO Abbreviation: Nat. Rev. Cancer Publication Date: 2013 Jan |
Date Detail:
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Created Date: 2013-1-10 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 101124168 Medline TA: Nat Rev Cancer Country: - |
Other Details:
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Languages: ENG Pagination: - Citation Subset: - |
Affiliation:
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1] Center for Genomic Science of IIT@SEMM, Fondazione Istituto Italiano di Tecnologia (IIT), Via Adamello 16, 20139 Milan, Italy. [2]. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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