Effects Of Pin Biomechanics, Coating Material And Surface Roughness On The Pin-bone Interface In External Repair
Funder
National Health and Medical Research Council
Funding Amount
$470,000.00
Summary
Some fractures require external fixation, anchored with metal pins in the bone fragments. The reatment is generally successful, although the pin tracts often loosen and become infected. This complication may jeopardise fracture healing and must be treated. The purpose of this project is to determine what aspects of pin design predispose to these problems at the pin-bone interface. Is it the way the pins are initially inserted, perhaps not tightly enough so that the pin is unstable, or perhaps to ....Some fractures require external fixation, anchored with metal pins in the bone fragments. The reatment is generally successful, although the pin tracts often loosen and become infected. This complication may jeopardise fracture healing and must be treated. The purpose of this project is to determine what aspects of pin design predispose to these problems at the pin-bone interface. Is it the way the pins are initially inserted, perhaps not tightly enough so that the pin is unstable, or perhaps too tight, causing microcracks in the bone? Is it the material of the pin, which might be improved with a bioactive coating? Is it the surface roughness which causes different responses of bone cells? Would it help to have an antibiotic pin? This proposal is designed to answer these questions. The biomechanics of the pin will first be studied with computer models and then tested in the laboratory. The loosening and infection associated with different types of pin will then be studied biologically. The results of the study will clarify the roles of pin biomechanics, coating and surface roughness, leading to improvements in design and better outcomes in fracture patients.Read moreRead less
To understand the genetic basis of two of the most important cancers in women, breast and ovarian cancer. The team has already identified one gene that confers a very high risk of breast cancer and may account for a large proportion of 'familial' breast cancer. Their aim is to identify additional predisposition genes and to determine their normal function in the cell, as well as the way in which they contribute to the development of cancer
DNA Repair Mechanisms In The Pathogenesis Of Hepatocellular Carcinoma
Funder
National Health and Medical Research Council
Funding Amount
$339,078.00
Summary
Hepatocellular carcinoma (HCC) or cancer originating in the liver ranks 5th in worldwide frequency among tumours, and is the 3rd highest cause of cancer in our region. The incidence is increasing in most countries including Australia, Japan and USA. The overall prognosis is poor, with >80% affected persons dying from this disorder. The risk factors for HCC are well known and include chronic hepatitis B or C virus infection, alcoholism and liver iron accumulation. Despite the vast amount of in ....Hepatocellular carcinoma (HCC) or cancer originating in the liver ranks 5th in worldwide frequency among tumours, and is the 3rd highest cause of cancer in our region. The incidence is increasing in most countries including Australia, Japan and USA. The overall prognosis is poor, with >80% affected persons dying from this disorder. The risk factors for HCC are well known and include chronic hepatitis B or C virus infection, alcoholism and liver iron accumulation. Despite the vast amount of information available regarding these risk factors, the way in which they alter normal liver cells to make them cancerous remains undefined. The majority of liver cancers, regardless of cause, develop in severely scarred, or cirrhotic liver in the presence of chronic liver inflammation. Such an environment causes liver cells, which are usually stable and not dividing, to continue replicating in response to injury; such continued cell division can lead to damaged genetic information in the DNA of these cells. Many cancers are associated with chromosomal damage, including broken ends and deleted genetic material. The main focus of this project to investigate how defective repair of disrupted genetic information contained in DNA of chromosomes in damaged liver cells contributes to the development of liver cancer. Using mice lacking specific genetic information to repair DNA double strand breaks, we plan to investigate whether abnormalities in DNA repair mechanisms in liver cells damaged by diethylnitrosamine (DEN) predisposes liver cells to regenerate abnormally thereby progressing to cancer. We have clues that 7 specific sites in chromosomes where loss of key genes may promote HCC formation. These studies will greatly enhance our understanding of the molecular basis by which HCC develops. The ultimate goal of this research is to develop effective screening and treatment strategies to prevent or interrupt the process of liver cancer development in at-risk individuals.Read moreRead less