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Targeting APL fusion proteins by peptide interference.

Targeting APL fusion proteins by peptide interference. Research Abstract Details 

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  • Targeting APL fusion proteins by peptide interference. Abstract Text:

    a melnickA Melnick,

    A significant barrier to experimental therapeutics is the ability to identify and specifically target oncogenic proteins involved in the molecular pathogenesis of disease. In acute promyelocytic leukemia (APL), aberrant transcription factors and their associated machinery play a central role in mediating the malignant phenotype. The mechanism of action of APL chimeric fusion proteins involves their ability to either self-associate or interact with different partner proteins. Thus, targeting protein-protein interactions could have a significant impact in blocking the activity of APL oncoproteins. As therapeutic targets, the interface between interacting proteins may not always be amenable to highly specific small molecule blockade. In contrast, peptides are well-suited to this purpose and can be reliably delivered when fused to cell-permeable peptide domains. Therapeutic peptides can be designed to directly target APL fusion proteins, their downstream effectors, or other potentially synergistic oncogenic mechanisms of importance in APL blasts. In addition to serving as potential therapeutic agents, such reagents could serve as powerful reagents to dissect the molecular pathogenesis of APL.

    Targeting APL fusion proteins by peptide interference. Publishing Authors By Initials

    a melnickA Melnick,

    For similar biological phenomena, cell phenomena, and immunity: cell physiology: cell communication: signal transduction research abstracts see: biological phenomena, cell phenomena, and immunity: cell physiology: cell communication: signal transduction research

    PUBMED ID PMID:

    MEDLINE DATE:

    Targeting APL fusion proteins by peptide interference. Journal Published:

    PUBLICATION TYPE: Review

    Journal: Current topics in microbiology and immunology

    VOLUME: 313

    Page Numbers: 221-43

    Journal Abbreviation: Curr. Top. Microbiol. Immunol.

    ISSN: 0070-217X

    DAY: 3

    MONTH: 12

    YEAR: 2007

    Targeting APL fusion proteins by peptide interference. Information

    Number of References: 90

    LANGUAGE: eng

    NlmUniqueID: 110513

    Targeting APL fusion proteins by peptide interference. Keywords Mesh Terms:

    KEYWORDS: Signal Transduction

    MESH TERMS: physiology

    Chemical & Substance for Abstract: Targeting APL fusion proteins by peptide interference. Information

    Substance Name: promyelocytic leukemia-retinoic acid rec

    Registry Number: 0

    Grant and Affiliation Information for Targeting APL fusion proteins by peptide interference.

    AFFILIATION: Department of Developmental and Molecular Biology and Medical Oncology, Albert Einstein College of Medicine, 1300 Morris Park Ave, Bronx, NY 10461, USA. amelnick@aecom.yu.edu

    Country: Germany

    Germany Research PublicationGermany Research Publication

    AGENCY: United States NCI

    GRANT: R01 CA104348

    ACRONYM: CA

    MEDLINETA: Curr Top Microbiol Immunol

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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