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Field of Research : Cancer Cell Biology
Status : Closed
Research Topic : METASTASIS
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  • Funded Activity

    Parathyroid Hormone-related Protein (PTHrP), Common Genetic Variants In The PTHrP Gene (PTHLH), And Breast Cancer Risk And Survival

    Funder
    National Health and Medical Research Council
    Funding Amount
    $120,253.00
    Summary
    In a partnership between Peter MacCallum Cancer Centre, St Vincent's Hospital, and The University of Melbourne, we are investigating the role of PTHrP, a peptide integral to the growth and spread of Cancer. Initially thought to facilitate cancer spread, recent studies suggest it may actually be protective. In a new approach, we will analyse new DNA databases and patient data from around the world. We hope to extend our understanding of PTHrP, and perhaps find novel drug and therapeutic targets.
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    Funded Activity

    Uncovering The Role Of Collecting Lymphatic Vessels In Cancer.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $688,875.00
    Summary
    Lymphatic vessels are a critical part of the circulatory system, allowing the return of fluid and cells that escape the blood vessels, and playing an intimate role in the body's immune function. In cancer, the lymphatic vessels serve as conduits for the transport of tumour cells to lymph nodes and may contribute to distant metastasis. Our study is designed to understand the role played by major collecting lymphatic vessels in cancer and to identify molecules that control their activity.
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    Funded Activity

    Transient Tissue ‘priming’ Via FAK Inhibition To Impair Pancreatic Cancer Progression And Improve Sensitivity To Gemcitabine/Abraxane

    Funder
    National Health and Medical Research Council
    Funding Amount
    $643,848.00
    Summary
    The success of cancer drugs is dependent on many factors including the properties of the tumour tissue. As a tumour grows it changes the tissue around it, and this affects response to treatment. Combining classical biology with engineering to generate 3D models that mimic tumours, along with cutting-edge imaging technology and mouse models, we will target FAK-controlled cancer cell pathways that sense tissue changes, together with already approved cancer drugs to improve patient outcome.
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    Funded Activity

    Vitamin D Deficiency And Breast Cancer Metastasis To Bone

    Funder
    National Health and Medical Research Council
    Funding Amount
    $300,413.00
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    Funded Activity

    Single-cell Optical Window Imaging In CDK1-FRET Biosensor Mice To Assess Tissue Stiffness And Optimise Delivery And Therapeutic Response To Gemcitabine/Abraxane In Pancreatic Cancer.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $676,979.00
    Summary
    Inefficient drug response in solid tumour tissue is commonly a limiting factor in the clinical effectiveness of cancer therapies. Using cutting-edge imaging technology and 3D models that mimic the disease, we have mapped areas of poor drug response within distinct regions of tumours. Here, we pinpoint and specifically target key factors limiting efficient drug targeting in order to improve the encouraging anti-cancer profile of the new drug combination Gemcitabine/Abraxane in pancreatic cancer.
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    Funded Activity

    Real-time Optical Window Imaging Of AKT-FRET Biosensor Mice To Maximise PI3K/AKT Drug Targeting Within The Hypoxic Microenvironment Of Pancreatic Cancer.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $683,447.00
    Summary
    Inefficient drug response in solid tumour tissue is often a limiting factor in the clinical effectiveness of cancer therapies. Using cutting-edge imaging technology and 3D models that mimic the disease, we have mapped areas of poor drug response within distinct regions of tumours with low oxygen levels known as hypoxia. Here, we will specifically target factors limiting efficient drug targeting in these areas to improve the encouraging anti-cancer profile of AKT inhibitors in pancreatic cancer.
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    Funded Activity

    Live FRET Imaging To Visualize Drug Targeting In Combination With Stromal Therapy In Pancreatic Cancer: Optimising Anti-invasive Treatment.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $690,356.00
    Summary
    Here we use nanotechnology (tiny biosensors) to monitor and improve drug delivery to solid tumours in pancreatic cancer.
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    Funded Activity

    Biosensor Imaging In Preclinical Pancreatic Cancer Targeting: Taking Cancer Targeting To New Dimensions.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $640,210.00
    Summary
    Using cutting-edge imaging technology and 3D models that mimic cancer, we can map areas of poor drug response within distinct 'stages' or regions of tumours. Here, we pinpoint and specifically target key factors limiting efficient drug response in order to improve the encouraging anti-cancer profile of new or current drugs in pancreatic cancer.
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    Funded Activity

    PARP And PI3K Inhibition In Pancreatic Cancer: Intravital Insights And ‘fine-tune’ Priming Using AKT And Single/double-strand DNA Break Biosensor Mice.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $760,505.00
    Summary
    Inefficient drug response in solid tumour tissue is often a limiting factor in the clinical effectiveness of cancer therapies. Using cutting-edge imaging technology and 3D models that mimic the disease, we can map areas of poor drug response within distinct regions of tumours with chemotherapy. Here, we will shift factors limiting efficient drug targeting in these areas to improve the encouraging anti-cancer profile of PI3K and DNA repair inhibitors in pancreatic cancer.
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    Funded Activity

    Investigating Signalling Pathways That Mediate Suppression Of Anoikis By Chemokine Receptors In Metastatic Breast Cancer Cells

    Funder
    National Health and Medical Research Council
    Funding Amount
    $597,349.00
    Summary
    This research aims at understanding the "nuts and bolts" of the main killer in cancer patients - tumour metastasis. We will look for molecules that are specific to metastatic tumour cells that transmit signals from the cell surface to the cell "suicide" machinery and prevent metastatic cancer cell death.
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    Showing 1-10 of 28 Funded Activites

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