The lining of the uterus is unusual compared to other parts of the adult body in that new blood vessels grow and then breakdown during menstruation every month. The aim of this project is to understand what controls the growth and regression of these uterine blood vessels. This information is of immediate relevance to a number of clinical problems where an ability to either promote or prevent blood vessel growth would be of major advantage. For example, increased blood vessel growth would accele ....The lining of the uterus is unusual compared to other parts of the adult body in that new blood vessels grow and then breakdown during menstruation every month. The aim of this project is to understand what controls the growth and regression of these uterine blood vessels. This information is of immediate relevance to a number of clinical problems where an ability to either promote or prevent blood vessel growth would be of major advantage. For example, increased blood vessel growth would accelerate wound healing, while blocking blood vessel growth would prevent the growth and spread of cancers. Another disorder that could be controlled through preventing blood vessel growth is endometriosis, a disease where cells from the lining of the uterus grow inside the abdomen causing pain and infertility. Endometriosis affects upto 10% of women.Read moreRead less
The main complications of pregnancy, preeclampsia, preterm birth and intrauterine growth restriction affliict 19% of first pregnancies and are life threatening to the mother or baby in 6% of pregnancies. They are associated with poor placental invasion of the uterus. We aim to further elucidate the molecular mechanisms involved in placental invasion and proper placental development to identify possible targets for future treatments to improve the health of pregnant women and babies.
OVARIAN CANCER METASTASIS: Unraveling The Biology Of The Plasminogen Activation Cascade
Funder
National Health and Medical Research Council
Funding Amount
$169,875.00
Summary
Ovarian cancer affects 1,200 new Australians every year. Compared to breast cancer where research education and early screening have improved mortality rates, the incidence of ovarian cancer has not improved and death rates have more than doubled since 1930. With few overt symptoms, ovarian cancer has an extremely poor prognosis - a staggering 71% of women diagnosed with ovarian cancer will die from the disease, compared to 21% for breast cancer. Any studies which increase our understanding of t ....Ovarian cancer affects 1,200 new Australians every year. Compared to breast cancer where research education and early screening have improved mortality rates, the incidence of ovarian cancer has not improved and death rates have more than doubled since 1930. With few overt symptoms, ovarian cancer has an extremely poor prognosis - a staggering 71% of women diagnosed with ovarian cancer will die from the disease, compared to 21% for breast cancer. Any studies which increase our understanding of the biology of ovarian cancer metastasis may lead to new therapies designed to control these processes - as such this would be a major inroad into our fight against this cancer. The aim of this novel research project is to unravel the role that one cell surface system (the plasminogen (Plg) activation cascade) plays in determining the ability of ovarian cancer cells to metastasise and regulate new tumour blood vessel formation. This study addresses the paradoxical observations that this cascade can simultaneously facilitate cancer metastasis whilst concomitantly stopping new blood vessel formation in tumours. Using a number of advanced molecular cell biology methods, the hypothesis we will test is that the capacity of ovarian cancer to metastasise is determined by differential processing of plasminogen subsequent to cell-surface Plg binding. This results in a delicate balance between the generation of cell surface proteases and the release of protein fragments capable of stopping tumour blood vessel growth. Our group is well-equipped to address this hypothesis since we have already shown that: (1) Plg binding and activation is required for cancer cell invasion; (2) Plg binding and activation is elevated on malignant compared to benign cancers (3) Plg unfolds after it binds to cell surfaces or recombinant receptors; and, (4) Plg is easily fragmented to products that inhibit new blood vessel formation after binding to some cancer cells.Read moreRead less