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NOTCH and PI3K-AKT pathways intertwined.

NOTCH and PI3K-AKT pathways intertwined. Research Abstract Details 

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  • NOTCH and PI3K-AKT pathways intertwined. Abstract Text:

    alejandro gutierrezAlejandro Gutierrez,a thomas lookA Thomas Look,alejandro gutierrezAlejandro Gutierrez,a thomas lookA Thomas Look,

    Constitutive signaling by the NOTCH1 receptor contributes to more than half of all cases of T cell acute lymphoblastic leukemia (T-ALL). However, blocking the proteolytic activation of NOTCH1 with gamma-secretase inhibitors (GSIs) fails to alter the growth of some T-ALL cell lines carrying the mutated receptor. A recent report by Palomero et al. in Nature Medicine identifies loss of PTEN as a critical event leading to resistance to NOTCH inhibition, which causes the transfer of "oncogene addiction" from the NOTCH1 to the PI3K/AKT pathway. This novel observation suggests the need to simultaneously inhibit both pathways as a means to improve therapeutic efficacy in human T-ALL.

    NOTCH and PI3K-AKT pathways intertwined. Publishing Authors By Initials

    a gutierrezA Gutierrez,at lookAT Look,a gutierrezA Gutierrez,at lookAT Look,

    For similar abstracts research abstracts see: abstracts research

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    NOTCH and PI3K-AKT pathways intertwined. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Cancer cell

    VOLUME: 12

    Page Numbers: 411-3

    Journal Abbreviation:

    ISSN: 1535-6108

    DAY: 12

    MONTH: Nov

    YEAR: 2007

    NOTCH and PI3K-AKT pathways intertwined. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 101130617

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    Grant and Affiliation Information for NOTCH and PI3K-AKT pathways intertwined.

    AFFILIATION: Department of Pediatric Oncology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Cancer Cell

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