LIVER CANCER & PATIENT-DERIVED TUMOUR ORGANOIDS
With
Dr Benjamin Dwyer,
Senior Research Fellow &
Director, Western Australian Organioid Innovation Hub,
Curtin Medical Research Institute,
Curtin University, Western Australia
RESEARCHER PROFILE
Filmed in Perth, Western Australia | February 2026
Dr Benjamin Dwyer is a translational cancer researcher driven by a clear purpose: to ensure discoveries made in the laboratory genuinely improve outcomes for patients.
Based at Curtin University, he established and now leads the organoid platform within the Liver Cancer Collaborative and directs the WA Organoid Innovation Hub, working at the intersection of biology, medicine and biotechnology to accelerate new treatments for liver cancer.
After completing his PhD in Perth, Dr Dwyer joined the world-leading liver research group of Prof Stuart Forbes at the University of Edinburgh, where he contributed to research spanning fundamental biology, clinical trials and commercial translation. He helped define how cholangiocarcinoma crosstalk with macrophages establishes a protective environment. In parallel, he was closely involved in the development of macrophage cell therapy for cirrhosis as part of the management team of the MATCH trials, and established novel, GMP-compatible methods to engineer and cryopreserve therapeutic macrophages, foundational methods for the commercial development of macrophage therapy. He was part of the founding team of a biotechnology spinout created to translate this work, and the therapeutic strategy built on those early methods is now progressing through Phase 1 clinical testing. Seeing principles he helped establish move from bench to bedside has been a defining milestone in his career.
Today, as part of the Liver Cancer Collaborative his research focuses on building patient-derived “mini tumours” for drug development that better predict treatment response, narrowing the gap between laboratory models and real patient outcomes.
COLLABORATIONS WITH:
Perkins Cancer Biobank, Australian Centre for RNA Therapeutics in Cancer, UWA, WA Data Science Innovation Hub, Murdoch University, Epichem, Cholangiocarcinoma Foundation Australia WEHI National Drug Discovery Centre, Inventia Life Sciences, University of Edinburgh, Scottish National Blood Transfusion Service (SNBTS), University of Calgary
FUNDING FROM:
Department of Health WA FHRI Fund, Cancer Research Trust, Gastroenterological Society of Australia (GESA), Ian Potter Foundation, AMMF- The Cholangiocarcinoma Charity,
Source: Supplied and adapted
You Might also like
-
Elite athlete physical and mental health impact performance
Understanding the interaction between genes and lifestyle factors in response to stress can lead to potential therapeutic interventions for stress-related disorders. This research is crucial for promoting health and well-being.
Professor Mehta has recently commenced research into elite athlete physical and mental health impact performance, with research at the intersection of statistics, genomics, and mental health. This research is ahead of, and in anticipation of, the Summer Olympics in Brisbane in 2032.
-
Identifying and treating autoimmune neurological disorders
Associate Professor Sudarshini Ramanathan is a neurologist and clinician scientist whose work focuses on autoimmune neurological disorders. Her research has helped identify new neurological syndromes due to antibody-mediated demyelination and encephalitis, and improve diagnostic tools and treatment guidelines for patients with autoimmune diseases affecting the brain, spinal cord, muscles and nerves.
-
Causal genes and pathogenic mechanisms underlying gastrointestinal diseases
Professor D’Amato has more than 25 years research experience in the field of human genetics and complex diseases, with activities most recently geared towards a translational application for therapeutic precision in gastroenterology. His team, the Gastrointestinal Genetics Laboratory, combine leading expertise in genomic, computational and pre-clinical research, and have contributed important breakthroughs linking specific genes and pathogenetic mechanisms to a number of gastrointestinal diseases like inflammatory bowel disease (IBD), microscopic colitis (MC) and irritable bowel syndrome (IBS).
https://orcid.org/0000-0003-2527-5417