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Scheme : Project Grants
Research Topic : primitive neuroectodermal tumours
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  • Funded Activity

    A 2:1 Randomised Phase II Study Of NivolUmab And Temozolomide Vs Temozolomide In Methylated Newly Diagnosed Elderly Glioblastoma (NUTMEG)

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,608,845.00
    Summary
    Radiotherapy and Temozolomide (TMZ) chemotherapy treatment for the brain tumour glioblastoma (GBM) is not as effective in elderly patients. If their tumour has a genetic marker called "methylated MGMT", TMZ does work relatively better and is often given alone. Elderly GBM patients with this marker will be randomly selected in this trial to have TMZ alone or TMZ + Nivolumab - a drug that assists the immune system to attack cancer.
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    Funded Activity

    Targeting Mitochondrial Metabolism In Diffuse Intrinsic Pontine Gliomas As A Novel Therapeutic Strategy

    Funder
    National Health and Medical Research Council
    Funding Amount
    $607,796.00
    Summary
    Diffuse Intrinsic Pontine Glioma (DIPG) represents the most aggressive cancer of childhood, with no effective treatments available, and almost all children dying within one year of diagnosis. We have successfully grown the first DIPG cells in the laboratory and found a new approach to attack them, by specifically targeting the cell's power source - the mitochondria. We will build on these findings and develop this treatment strategy with the aim to make this novel therapy available to children w .... Diffuse Intrinsic Pontine Glioma (DIPG) represents the most aggressive cancer of childhood, with no effective treatments available, and almost all children dying within one year of diagnosis. We have successfully grown the first DIPG cells in the laboratory and found a new approach to attack them, by specifically targeting the cell's power source - the mitochondria. We will build on these findings and develop this treatment strategy with the aim to make this novel therapy available to children with this deadly disease.
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    Funded Activity

    Contribution Of Ovarian Cancer Stem Cells To Chemoresistance And Recurrent Disease.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $378,940.00
    Summary
    Ovarian cancer is the most lethal gynaecological cancer. Previously, we showed that cancer stem cells are the “beating heart” of the ovarian cancer and are responsible for drug resistance and tumour relapse. The ineffective targeting of these cells by chemotherapy is accountable for the poor clinical outcomes in ovarian cancer patients. This project will define the molecular signals involved in maintenance of cancer stem cells and develop targeted therapies against these cells.
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    Funded Activity

    Nfib Regulates Glial Differentiation During Development And Disease Via Repression Of The Key Epigenetic Protein, Ezh2

    Funder
    National Health and Medical Research Council
    Funding Amount
    $572,912.00
    Summary
    Glial development is critical during development, and unrestrained proliferation of glial stem cells in the adult can lead to deadly brain cancers such as glioma. At present there is no cure for glioma and current treatments do not significantly delay tumour progression. Nfib is a transcription factor that may prevent tumour growth through cellular differentiation. We will investigate the role of Nfib during development and in the pathogenesis of glioma and its potential as a therapeutic target.
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    Funded Activity

    Control Of Gastrointestinal Tumour Progression By Therapeutic Interference With Myeloid Derived Cells

    Funder
    National Health and Medical Research Council
    Funding Amount
    $758,678.00
    Summary
    Cancers of the stomach and the colon are a major health burden. Despite our increased molecular understanding of the mutation that cause these cancers our treatment options are very limited. Here we will use sophisticated and validated mouse models for these cancers to establish how blood-borne cells contribute to the growth and spreading of these cancer. We will use these models to establish highly effective treatment combinations of therapeutic agents that are already undergoing preclinical te .... Cancers of the stomach and the colon are a major health burden. Despite our increased molecular understanding of the mutation that cause these cancers our treatment options are very limited. Here we will use sophisticated and validated mouse models for these cancers to establish how blood-borne cells contribute to the growth and spreading of these cancer. We will use these models to establish highly effective treatment combinations of therapeutic agents that are already undergoing preclinical testing.
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    Funded Activity

    CHARACTERIZATION OF A NEW SUBTYPE OF AGGRESSIVE BREAST CANCER

    Funder
    National Health and Medical Research Council
    Funding Amount
    $763,152.00
    Summary
    Much effort has been invested in the sequencing of cancer genomes, leading to the identification of genes linked to aggressive subtypes. There is now a need to confirm the importance of these genes and to exploit these findings for patient therapies. We have identified a new cancer driver controlling an aggressive type of breast tumour which may act through one carbon/folate metabolism. We aim to map the inner workings of these cancers to devise effective targeted drugs for these patients.
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    Funded Activity

    Developing Irreversible Electroporation Non-Thermal Tumor Ablation For Organ-Confined Prostate Cancer Treatment

    Funder
    National Health and Medical Research Council
    Funding Amount
    $290,512.00
    Summary
    IRE is technique for targeted tissue ablation. Electrodes placed into the targeted area deliver intense, brief electric pulses. Nano-scale pores are created in the cell membrane killing the cells but preserving the extracellular matrix. The pulses do not affect sensitive structures including neurovascular bundles, major vasculature and ductal systems preserving their function. It may address prostate regions implicated in prostate cancer without damaging vital structures, reducing side effects.
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    Funded Activity

    Targeting The PD-1 Pathway In Osteosarcoma

    Funder
    National Health and Medical Research Council
    Funding Amount
    $650,813.00
    Summary
    Osteosarcoma is the most common tumour of bone. Recent success in targeting immune checkpoint blockers such as Programmed death-1 (PD-1) in genomically complex tumours suggests that osteosarcomas may be amenable to such strategies. We will characterise the role of the PD-1 pathway in osteosarcoma development and growth. Using preclinical mouse models we will investigate the biology of the PD-1 pathway and study its potential as a therapeutic target in advanced and resectable osteosarcoma.
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    Funded Activity

    A Prospective Study Of Language Impairment And Recovery Following Surgery For Brain Tumours

    Funder
    National Health and Medical Research Council
    Funding Amount
    $861,342.00
    Summary
    This multi-site project will investigate the incidence and nature of post-operative language difficulties (aphasia) in patients following surgery for left hemisphere primary brain tumours. It will provide comprehensive data concerning risk factors for post-surgical aphasia in Australian patients, in addition to important information about the brain lesions responsible for its various clinical presentations. This information will be used to generate recommendations for clinical practice.
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    Funded Activity

    The Development Of Innovative Multiplexed Molecular Imaging Technology Targeting Improved Diagnostic Imaging Of Glioblastoma Multiforme

    Funder
    National Health and Medical Research Council
    Funding Amount
    $403,599.00
    Summary
    Glioblastoma Multiforme (GBM) is extremely invasive and the most lethal of all primary brain tumours. To optimise treatment planning, we propose to develop novel Multiplexed Molecular Imaging (MMI) technology employing the latest PET-MRI hybrid imaging technology. Our strategy targets the development of new F19 MRI MI agents for measuring tumour infiltration that can be multiplexed with F18 PET hypoxia tracers. Our MI agents can also act as conjugative vehicles for drug delivery.
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    Showing 1-10 of 17 Funded Activites

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