• Novel approach could lead to treatment o

    From ScienceDaily@1:317/3 to All on Mon May 9 22:30:42 2022
    Novel approach could lead to treatment of devastating brain tumors


    Date:
    May 9, 2022
    Source:
    University of Surrey
    Summary:
    Findings from a seven-year research project suggests that there
    could be a new approach to treating one of the most common and
    devasting forms of brain cancer in adults -- Glioblastoma Multiforme
    (GBM).



    FULL STORY ========================================================================== Findings from a seven-year research project suggests that there could
    be a new approach to treating one of the most common and devasting forms
    of brain cancer in adults -- Glioblastoma Multiforme (GBM).


    ==========================================================================
    In a peer-reviewed study published by BMC Cancer,scientists from the
    University of Surrey show that a short chain of amino acids (the HTL-001 peptide) is effective at targeting and inhibiting the function of a
    family of genes responsible for the growth of GBM -- Hox genes. The
    study was conducted in cell and animal models.

    The HTL-001 peptide used in the study has undergone safety testing and
    is suitable for patient trials. These trials are now being considered
    in GBM and other cancers.

    Hardev Pandha, project lead and Professor of Medical Oncology at
    the University of Surrey, said: "People who suffer from Glioblastoma
    Multiforme have a five per cent survival rate over a five-year period --
    a figure that has not improved in decades.

    While we are still early in the process, our seven-year project offers
    a glimmer of hope for finding a solution to Hox gene dysregulation,
    which is associated with the growth of GBM and other cancers, and which
    has proven to be elusive as a target for so many years." Ironically,
    Hox genes are responsible for the healthy growth of brain tissue but
    are ordinarily silenced at birth after vigorous activity in the growing
    embryo. However, if they are inappropriately 'switched on' again, their activity can lead to the progression of cancer. Hox gene dysregulation
    has long been recognised in GBM.

    The project was carried out in collaboration with the universities of
    Surrey, Leeds and Texas, and HOX Therapeutics, a University of Surrey
    start-up company based on the University's Surrey Research Park.

    Professor Susan Short, co-author of the study from the University
    of Leeds, said: "We desperately need new treatment avenues for these
    aggressive brain tumours.

    Targeting developmental genes like the HOX genes that are abnormally
    switched on in the tumour cells could be a novel and effective
    way to stop glioblastomas growing and becoming life-threatening."
    James Culverwell, CEO of HOX Therapeutics, said: "HOX Therapeutics
    is excited to be associated with this project and we hope that with
    our continuing support, this research will eventually lead to novel and effective treatments for both brain and other cancers where HOX gene over- expression is a clear therapeutic target."

    ========================================================================== Story Source: Materials provided by University_of_Surrey. Note: Content
    may be edited for style and length.


    ========================================================================== Journal Reference:
    1. Einthavy Arunachalam, William Rogers, Guy R. Simpson, Carla Mo"ller-
    Levet, Gemma Bolton, Mohammed Ismael, Christopher Smith, Karl
    Keegen, Izhar Bagwan, Tim Brend, Susan C. Short, Bangxing Hong,
    Yoshihiro Otani, Balveen Kaur, Nicola Annels, Richard Morgan,
    Hardev Pandha. HOX and PBX gene dysregulation as a therapeutic
    target in glioblastoma multiforme.

    BMC Cancer, 2022; 22 (1) DOI: 10.1186/s12885-022-09466-8 ==========================================================================

    Link to news story: https://www.sciencedaily.com/releases/2022/05/220509100942.htm

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