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Research Topic : Steroid hormones
Field of Research : Endocrinology
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  • Funded Activity

    Impact Of Progesterone Receptor Subnuclear Localisation On Progesterone Action In Endocrine Target Cells

    Funder
    National Health and Medical Research Council
    Funding Amount
    $459,514.00
    Summary
    Breast cancer affects 10,000 Australian women annually and is a major cause of cancer death. The hormone progesterone, which is produced by the ovaries in women, is responsible for some aspects of the development of the normal breast in women and is also implicated in the development and response of breast and endometrial cancers. In normal cells progesterone acts via a specific protein (or receptor) in the nucleus, and we have shown that this protein accumulates into foci when it is active. We .... Breast cancer affects 10,000 Australian women annually and is a major cause of cancer death. The hormone progesterone, which is produced by the ovaries in women, is responsible for some aspects of the development of the normal breast in women and is also implicated in the development and response of breast and endometrial cancers. In normal cells progesterone acts via a specific protein (or receptor) in the nucleus, and we have shown that this protein accumulates into foci when it is active. We have noticed that in cancers, this accumulation is disrupted, and this is a bad sign for the cancer. As breast cancer develops, it causes many dramatic changes in the structure of cells of the breast, and particularly in the nucleus, which carries the genetic information that programs cancer cell behaviour. The nucleus normally is highly organised into compartments, which carry out different functions of the cell, such as duplication of the DNA, repair of DNA after damage, and switching on and off of particular genes important to the function of the cell. This organisation is altered dramatically in cancer cells, and it seems that this altered organisation is responsible for altered function. In this project we aim to work out what makes the receptor for progesterone form foci, how these foci are involved in the action of progesterone, and how the changed structure of the nucleus changes this process. This project will link the structure of the cell nucleus with the ability of progesterone to switch on or off particular genes, and this will provide the first signposts of how changes seen in cancer cell nuclei are reflected in changed hormonal signalling. Healthy women are regularly exposed to progestins in oral contraceptives and hormone replacement therapy. The known increased risk of breast cancer as a result of exposure to progestins creates an imperative to understand how progesterone may have aberrant effects. This project will address this important health issue.
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    Funded Activity

    The Role Of Male Hormones In Bone Cell Function

    Funder
    National Health and Medical Research Council
    Funding Amount
    $220,825.00
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    Funded Activity

    Development And Application Of A Novel Ultrasensitive LC-MS Estradiol Assay

    Funder
    National Health and Medical Research Council
    Funding Amount
    $240,400.00
    Summary
    This project will develop a new ultrasensitive method using liquid chromatography-mass spectrometry to measure extremely low level of circulating estrogens in the bloodstream especially in mice. This will allow for the first time the ability to study the natural regulation of fertility in mice and other sub-primate mammals for which the present assay methods are not adequate.
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    Funded Activity

    Women's Hormones And Health Across The Adult Life Span

    Funder
    National Health and Medical Research Council
    Funding Amount
    $951,005.00
    Summary
    Sex hormones are important in younger and older women’s health. However, normal levels of sex hormones for women of different ages and the extent to which sex hormones are associated with common health outcomes are yet to be established. These issues will be systematically studied in comprehensive, community-based studies of younger and older Australian women. The findings will be immediately translated into clinical practice guidelines and community education.
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    Funded Activity

    The Anorexia Of Ageing

    Funder
    National Health and Medical Research Council
    Funding Amount
    $122,608.00
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    Funded Activity

    In Vivo Regulators Of Androgen Receptor Function Inprostate Cancer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $311,081.00
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    Funded Activity

    Novel Ligand-Specific Interactions Enable Mineralocorticoid Receptor Modulation

    Funder
    National Health and Medical Research Council
    Funding Amount
    $835,005.00
    Summary
    The steroid hormone aldosterone controls salt balance and hence, blood pressure. It also has been shown to have a significant role in cardiac failure. Although drugs that block the aldosterone receptor are beneficial in the treatment of heart failure, they are limited by potassium retention in the kidney. In order to develop tissue-specific blockers of the aldosterone receptor, it is necessary to identify mechanisms by which the receptor can be activated and/or blocked in these tissues.
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    Funded Activity

    CHAPERONES IN BREAST CANCER AND ESTROGEN RECEPTOR FUNCTION

    Funder
    National Health and Medical Research Council
    Funding Amount
    $256,573.00
    Summary
    Resistance to hormone therapy in breast cancer is due to adaptations of estrogen signalling mechanisms that result in ERa activation causing growth. So, in the search for new treatments, we are looking for ways to remove ERa from the breast cancer cell. Our study addresses this major issue by focussing on Hsp90 molecular chaperone machinery that is essential for ERa function and in particular immunophilin 'helper' cochaperones that form part of receptor-Hsp90 complexes and fine-tune receptor res .... Resistance to hormone therapy in breast cancer is due to adaptations of estrogen signalling mechanisms that result in ERa activation causing growth. So, in the search for new treatments, we are looking for ways to remove ERa from the breast cancer cell. Our study addresses this major issue by focussing on Hsp90 molecular chaperone machinery that is essential for ERa function and in particular immunophilin 'helper' cochaperones that form part of receptor-Hsp90 complexes and fine-tune receptor responses to hormone. Through a novel mode of action, coumarin-based Hsp90 inhibitors disrupt Hsp90 dimerization causing receptor release and subsequent depletion. We will confirm this novel mechanism for new, high affinity Hsp90 inhibitors and determine which can best interfere with estrogen signalling, either alone or in combination with antiestrogen therapies in the treatment of hormone-dependent cancers. Our study has the potential to pin point the site of action of the immunophilins in ERa to a proline in a region critical for ligand-induced receptoractivation. We will determine the role of the immunophilins and this active-site proline residue in modulating receptor stability and function. Aberrant expression of receptor-associated immunophilins appears linked to endocrine resistance and metastasis in breast cancer. Our study will profile the expression of these chaperones in well defined breast cancer tissue microarrays, and has the potential to identify them as informative biomarkers in the treatment of the disease.
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    Funded Activity

    Hormonal Influences On Cells Of The Pituitary Gland

    Funder
    National Health and Medical Research Council
    Funding Amount
    $119,264.00
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    Funded Activity

    The Role Of Urotensin II In Diabetes-Associated Atherosclerosis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $405,594.00
    Summary
    People with diabetes most commonly die from stroke or heart attack and we need to determine what makes them more prone to these problems. The recently discovered UII system is increased in people with diabetes and has been found in diseased parts of blood vessels. Thus, the aim of this project is to characterise the UII system in the setting of diabetes using 2 unique genetically altered mice and a blocker a to study the effects of high cholesterol, diabetes and a deletion of UII.
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    Showing 1-10 of 32 Funded Activites

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