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Research Topic : notch
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  • Funded Activity

    The Role Of Notch And Hedgehog Signalling Pathways In The Development And Progression Of Breast Cancer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $37,324.00
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    Funded Activity

    Characterising The Physiological Roles Of The Asparaginyl Hydroxylase FIH-1 In Development And Disease.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $274,743.00
    Summary
    FIH-1 is an oxygen-sensing protein expressed in every cell. The ability for cells to detect and respond to oxygen deficiency is necessary for survival in heart disease and stroke, and is also a feature of cancer. This research aims to characterise the role FIH-1 plays in normal development and disease using mouse and tumour model systems. This research could ultimately indicate whether FIH-1 is a feasible drug target.
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    Funded Activity

    The Role Of Notch Numb Interactions In The Control Of Asymmetric Cell Division In Adult Neural Stem Cells

    Funder
    National Health and Medical Research Council
    Funding Amount
    $297,327.00
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    Funded Activity

    Heterogeneity In Processing And Signalling By The Notch Family Of Receptors In Vascular Development And Remodelling.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $85,716.00
    Summary
    Formation and remodelling of the blood vessels is a critical feature of development. In addition, numerous disorders including psoriasis, arthritis, blindness, heart and brain ischemia, neurodegeneration, hypertension, pre-eclampsia, respiratory distress and osteoporosis among others are characterised by defective blood vessel patterning. The significance associated with understanding how Notch genes direct blood vessel formation is paramount, as this knowledge will inform future research.
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    Funded Activity

    Humanisation And Pre-clinical Validation Of A Therapeutic Anti-cancer Antibody

    Funder
    National Health and Medical Research Council
    Funding Amount
    $699,136.00
    Summary
    This grant will develop a novel antibody against a protease expressed on cancer cells. Preclinical studies, and antibody humanisation, will be performed. This project will also provide vital information on optimal therapeutic approaches with the antibody that can be ultimately taken into human trials.
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    Funded Activity

    Antibody-based Inhibition Of ADAM10 As Cancer Immunotherapy

    Funder
    National Health and Medical Research Council
    Funding Amount
    $652,788.00
    Summary
    Despite our advances in understanding the molecular basis of cancer, treatments for metastatic cancers are limited, emphasising an urgent need for strategies targeting several oncogenic pathways. We generated monoclonal antibodies effectively blocking the activity of ADAM10, an oncogenic cell surface protease that activates tumour growth, invasion and metastasis through multiple pathways. Here we describe the strategies that progress these antibodies as lead therapeutics for clinical testing.
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    Funded Activity

    ADAM Metalloprotease Inhibition For Treatment Of Colorectal Cancer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $770,925.00
    Summary
    Colorectal cancer (CRC) causes over 4000 deaths/year, typically from developing drug resistance and spreading to other organs (metastasis). These processes involve tumour cells called cancer stem cells (CSCs), which rely on specific cell surface proteins for survival and function. We are developing antibodies against one of these type of proteins, to test in mouse models of CRC. These already show promise in targeting CSCs and inhibiting drug-resistance and metastasis in mice.
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    Funded Activity

    Investigating The Role Of The Notch4 Receptor In Blood Vessel Formation And Remodelling In Mammals

    Funder
    National Health and Medical Research Council
    Funding Amount
    $653,086.00
    Summary
    We aim to understand how blood vessels form. This process is crucial for foetal development, and for injury repair in adults. When there is too much or too little blood vessel formation, diseases such as arthritis, blindness and osteoporosis can result. Also many tumours grow and spread by growing new blood vessels. We will study a signal that occurs between cells (Notch signalling) that is important in controlling the amount of blood vessel formation, by analysing in detail one component (Notch .... We aim to understand how blood vessels form. This process is crucial for foetal development, and for injury repair in adults. When there is too much or too little blood vessel formation, diseases such as arthritis, blindness and osteoporosis can result. Also many tumours grow and spread by growing new blood vessels. We will study a signal that occurs between cells (Notch signalling) that is important in controlling the amount of blood vessel formation, by analysing in detail one component (Notch4)
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    Funded Activity

    Functional Analysis Of The Notch Signalling Pathway In The Differentiation And Maintenance Of Pituitary Progenitor Cells

    Funder
    National Health and Medical Research Council
    Funding Amount
    $421,320.00
    Summary
    Many of the processes that are essential for normal bodily function such as growth, the ability to cope with stress, sexual organ development, metabolism and milk production, are controlled by the pituitary gland. This organ is located at the base of the brain and regulates these bodily functions through the release of six different hormones. Formation of the pituitary gland occurs during development of the foetus. This process requires a specific set of genes that shape the pituitary and allow .... Many of the processes that are essential for normal bodily function such as growth, the ability to cope with stress, sexual organ development, metabolism and milk production, are controlled by the pituitary gland. This organ is located at the base of the brain and regulates these bodily functions through the release of six different hormones. Formation of the pituitary gland occurs during development of the foetus. This process requires a specific set of genes that shape the pituitary and allow the hormone secreting cells to arise. Changes in these pituitary formation genes results in underdevelopment of the pituitary in newborn babies. In severe cases, where the pituitary has failed to form completely (panhypopituitarism), these babies are extremely ill and in some instances do not survive. We are studying the genes that belong to the Notch signalling pathway. These genes are important regulators of cell differentiation during the development of the brain, skin, bone and many other tissues. However, the role of the Notch signalling genes in pituitary development is not known. We have shown for the first time that these genes are active during pituitary development. To test the function of these genes in the pituitary, we will generate mouse models that either lack or inappropriately activate these genes. Our results will provide insight into the role of Notch Signalling genes in pituitary development in mice and humans. In this project, we also hope to identify cells in the pituitary that are able to give rise to multiple hormone secreting cell types. These stem cells are of significant clinical importance as they provide an avenue for the development of novel therapies for pituitary disorders in humans, based on the replacement of defective pituitary tissue with functional stem cell derived tissue.
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    Funded Activity

    Role Of SLIRP In Colorectal Cancer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $547,315.00
    Summary
    Colon cancer causes about 4,000 deaths per year in Australia. A better understanding of the biology of colon cancer will lead to new therapeutics that will aim to overcome the treatment resistance. This project is focused on understanding how a novel protein SLIRP regulates colon cancer growth, and will investigate the mechanisms for its protective effects on the disease. If successful, these studies could provide the foundation for targeting SLIRP for therapeutics.
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    Showing 1-10 of 18 Funded Activites

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