Research

The profound symptoms of Parkinson’s are caused by accumulation of alpha-synuclein and the death of dopaminergic neurons. These are caused by defects in mitochondrial functioning, ubiquitin signalling and cell death mechanisms.

The Parkinson’s Disease Research Centre has brought together, in the same institute, world-leading experts in these areas to lead collaborative research and find a way to stop Parkinson’s.

WEHI has a decades-long history of leading research into why cells fail to die and instead form cancers, along with developing drugs to help. Now we’re flipping the science and using our expertise to stop neurons from dying in Parkinson’s disease.

Our expertise is focused on five pillars of research:

• biomarker discovery
• breakthrough discoveries
• drug discovery
• clinical trials
• advocacy

This approach, coupled with WEHI’s world-class platforms for drug development, medicinal chemistry, protein degradation technologies, bioinformatics and genomics, as well as our established links to the clinic, provides a unique position to identify new drug targets, and develop targeted new disease-modifying drugs to take to clinical trial.

A core aspect of our research is to understand neuronal cell death and how to prevent it. We are targeting specific mechanisms and pathways based on genes with known links to Parkinson’s.

Our labs are also at the forefront of understanding mitochondrial quality control in neurodegeneration and are looking at potentials for drug repurposing to establish if medications already approved for use in the clinic are effective against neurodegeneration.

To complement these projects our researchers in bioinformatics are working towards blood biomarkers as a diagnostic screening test.

We publish our research in highly regarded peer reviewed journals, a selection of which can be accessed in the links below.

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The intersection of collaborative research and emerging technology is where the next generation of Parkinson’s drugs will be found.

From culturing neurons in the lab that have Parkinson’s genetics using stem cells, to using artificial intelligence to accelerate research and access to genetic databases for Parkinson’s, advances in the tools we have at our disposal are beginning to unravel the complexity of Parkinson’s disease.

Central to our discoveries so far has been global research collaborations and access to funding from both grants and philanthropic donations.

We have neurologists from the Royal Melbourne Hospital’s Movement Disorders Clinic embedded as clinician researchers to bring the insights and firsthand experience of a healthcare perspective to the problem of finding a cure for Parkinson’s.

This ensures that as well as delivering fundamental scientific discoveries, we also have an approach to translating those discoveries into potential drug therapies through clinical trials.