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Sarcoma Translational Research

We aim to discover and develop safer and more effective treatments by doing inventive and rigorous research to improve outcomes for kids with cancer.

Our team features expertise across solid cancers - including sarcoma and immunotherapy research, using pre-clinical models, and systems immunology to address high relapse rates and develop innovative therapies for childhood cancers. 

Sarcoma and other solid cancer research 

Sarcomas are a heterogeneous group of cancers of the bone, muscle, or connective tissue. About 15% of cancers in children and adolescents are sarcomas, whereas only 1% of cancers in adults are sarcomas. Although many sarcomas can be cured with standard therapy, the relatively high incidence of the disease in younger people and the frequency of recurrence make the development of more effective therapies a high priority.

The Sarcoma Translational Research team aims to identify new treatments for young people with solid cancers. In particular, we are developing targeted therapies and immunotherapy approaches.  

Immunotherapy

In addition to sarcoma-specific research, our team includes researchers focused on developing immunotherapies that can be applied across a range of childhood cancers, such as brain cancer, leukaemia, and neuroblastoma. Immunotherapy is an exciting treatment that uses the body’s own immune system to fight cancer. While it has shown promising results in adults, there is a pressing need to adapt these therapies for children. We are working to address this gap by developing safer, more effective treatments that reduce or eliminate the need for toxic chemotherapies and radiotherapies. 

Through close collaboration across the laboratory and oncology clinic at Perth Children’s Hospital, we are discovering how to harness the immune system to target cancer more effectively.

Collaborative and innovative research 

To date, the treatment discovery approach for cancer has been incredibly adult-biased, which is reflected in the dismal number of new treatments approved for children. One important reason for this lack of progress is that in cancer drug discovery, children are treated as “small adults”. Without exception, therapies are developed in adult animal models, then tested in adult clinical trials, with trials in children only occurring later, if at all. Several exciting new therapies, including immunotherapy, are showing remarkable results for many adult cancers, with disappointing results in children. To tackle this challenge, the Centre has established world-first paediatric mouse models for all childhood cancer types, that more accurately represent the biology of kids. 

By bringing together expertise in sarcoma and other solid cancer biology, immunology, and our unique paediatric mouse models, we aim to discover groundbreaking treatments that will improve survival rates and long-term outcomes for children with sarcoma and other cancers. 

Team leader

Centre Head, Cancer; Head, Sarcoma Translational Research

Team members (23)

Postdoctoral Research Fellow

Postdoctoral Researcher

Dr Omar Elaskalani
Dr Omar Elaskalani

BSc, MSc, PhD

Senior Research Officer

Dr Emily Fletcher
Dr Emily Fletcher

BSc (Hons) MRes PhD

Senior Research Fellow

Dr Rachael Zemek
Dr Rachael Zemek

BSc (Hons), PhD

Honorary Research Associate

Breana Vitali

Breana Vitali

Postdoctoral Researcher

Sajla Singh

Sajla Singh

Research Assistant

Jenny Truong

Jenny Truong

Research Assistant

Xueting Ye

Xueting Ye

PhD Student

Neha Jain

Neha Jain

PhD Student

Jorren Kuster

Jorren Kuster

PhD Student

Samantha Barnes

Samantha Barnes

PhD Student

Cenxi Gao

Cenxi Gao

PhD Student

Juliet Schreurs

Juliet Schreurs

PhD Student

Wang Li

Wang Li

PhD Student

Iley Johnson

Iley Johnson

Medical Student

Hala Salih

Hala Salih

Masters Student

Hannah Smolders

Hannah Smolders

Masters Student

Jessica McQuillan

Jessica McQuillan

Masters Student

Febriana Ajelie

Febriana Ajelie

Casual Research Assistant

Francois Rwandamuriye

Francois Rwandamuriye

Honorary Team Member

Bree Foley

Bree Foley

Honorary Researcher

Sarcoma Translational Research projects

Featured projects

The interplay between sarcoma and surgery-induced wound healing

In this project, we are using systems biology approaches to map the wound healing response in sarcoma following surgery to identify new treatments that can prevent sarcoma relapse.

Local immunotherapy for sarcoma

We are developing a gel that can be left behind in the wound bed after sarcoma surgery.

Sarcoma Translational Research

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Publications

Reports and Findings

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Exploiting temporal aspects of cancer immunotherapy

Many mechanisms underlying an effective immunotherapy-induced antitumour response are transient and critically time dependent. This is equally true for several immunological events in the tumour microenvironment induced by other cancer treatments. Immune checkpoint therapy (ICT) has proven to be very effective in the treatment of some cancers, but unfortunately, with many cancer types, most patients do not experience a benefit. 

The MexTAg collaborative cross: host genetics affects asbestos related disease latency, but has little influence once tumours develop

This study combines two innovative mouse models in a major gene discovery project to assess the influence of host genetics on asbestos related disease (ARD). Conventional genetics studies provided evidence that some susceptibility to mesothelioma is genetic. However, the identification of host modifier genes, the roles they may play, and whether they contribute to disease susceptibility remain unknown.

Coupling of response biomarkers between tumor and peripheral blood in patients undergoing chemoimmunotherapy

Platinum-based chemotherapy in combination with anti-PD-L1 antibodies has shown promising results in mesothelioma. However, the immunological mechanisms underlying its efficacy are not well understood and there are no predictive biomarkers to guide treatment decisions.

Role of COL5A1 in lung squamous cell Carcinoma: Prognostic Implications and therapeutic potential

Lung squamous cell carcinoma (LUSC) is a significant health concern, characterized by a lack of specific therapies and limited treatment options for patients in advanced stages. This study aims to identify key molecules of prognostic importance in LUSC and provide an experimental foundation for their potential therapeutic applications.

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