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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

Head, Sarcoma Translational Research

Team members (21)

Postdoctoral Research Fellow

Postdoctoral Researcher

Dr Omar Elaskalani
Dr Omar Elaskalani

BSc, MSc, PhD

Senior Research Officer

Dr Rachael Zemek
Dr Rachael Zemek

BSc (Hons), PhD

Honorary Research Associate

Dr Breana Vitali

Dr Breana Vitali

Postdoctoral Researcher

Sajla Singh

Sajla Singh

Research Assistant

Jenny Truong

Jenny Truong

Research Assistant

Iley Johnson

Iley Johnson

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

Mishka Bayar

Mishka Bayar

Medical Student

Hannah Smolders

Hannah Smolders

Casual Research Assistant

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

Related video

Publications

Reports and Findings

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Comparative analysis of malignant pleural effusion and peripheral blood reveals unique T cell signatures associated with survival in mesothelioma patients

The success of cancer immunotherapies has highlighted the importance of monitoring the anti-tumour T cell response. Patients with mesothelioma frequently present with a malignant pleural effusion (MPE) that is commonly drained regularly to alleviate symptoms. As MPE contains tumour cells, T cells and cytokines, it provides a unique opportunity to sample immune events at the tumour site.

Rare Occurrence of Congenital Neuroblastoma and Tuberous Sclerosis

Pharmacological targeting and characterization of Voltage-Gated Sodium Channels (VGSCs) expressed in the high-grade glioma microenvironment

High-grade glioma (HGG) cells reactivate neurodevelopmental programs regulated by ion channels to drive tumor progression. The activity of voltage-gated sodium channels (VGSCs) is fundamental to development, a target of blood-brain barrier (BBB)-permeable FDA-approved drugs, and aids tumor advancement in several cancers. However, the contribution of VGSC activity to HGG pathology remains unknown.

CAR T cells targeting B7H3 demonstrate potent preclinical activity against AML and ESCC

T cells engineered to express chimeric antigen receptors (CARs) are a promising modality to treat refractory cancers. CD19 CAR-T therapy has achieved remarkable responses in against B-cell lymphomas, however, challenges persist for acute myeloid leukemia (AML) and solid malignancies. B7H3 is an immune regulatory molecule that is highly expressed in various tumor cells. Its abnormal expression in acute AML and esophageal squamous cell carcinoma (ESCC) is closely related to tumor progression. 

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