PANCREATIC AND LUNG CANCERS DRIVEN BY MUTATIONS IN THE CANCER GENE KRAS
Dr Mara Zeissig, Group Head, T Cell Immunotherapy Laboratory
Tumour Inflammation and Immunotherapy Program
SAiGENCI – South Australian immunoGENomics Cancer Institute, Australia
RESEARCHER PROFILE
Filmed in Adelaide, Australia | December 2025
Dr Mara Zeissig is a recently appointed Lab Head within the Tumour Inflammation and Immunotherapy Program at the South Australian immunoGENomics Cancer Institute (SAiGENCI).
Her research focuses on studying immune evasion mechanisms in lung and pancreatic cancers to identify novel ways to increase response to immunotherapy. Her expertise is in genetically engineered mouse models of lung cancer, CRISPR-Cas9 screening technologies and T cell based immunotherapies (e.g Checkpoint inhibitors).
Dr Zeissig obtained her PhD at the University of Adelaide in 2020 with Prof Andrew Zannettino, where her research focused on the role of chemokine receptor CCR1 in the dissemination of the hematological malignancy multiple myeloma. She then undertook postdoctoral studies at Monash University with Prof Tony Tiganis, focusing on the role of protein tyrosine phosphotases PTPN2 and PTP1B on anti-tumour immunity in melanoma, breast, colon and liver cancers. In 2022 she joined the lab of Prof Kate Sutherland at WEHI. Here she conducted sophisticated CRISPR-Cas9 in vitro and in vivo screening to identify genetic determinants that influence response to KRAS inhibitors, and to identify novel immunotherapy targets in KRAS-mutant lung cancer. Her research has been published in high-impact journals including Science Advances (2022) and Cancer Discovery (2022). Dr Zeissig has been the recipient of numerous career awards and grants, including a Victorian Cancer Agency ECR Fellowship (2023-2026) and a Cure Cancer Research Grant (2023).
Immunotherapies such as CAR T cell therapy or Immune checkpoint inhibitors all harness the ability of cytotoxic T cells to recognise and kill tumour cells. However, approx. 80% of solid cancer patients do not respond to immunotherapy. This is due to both tumour intrinsic and extrinsic evasion mechanisms, the most crucial of these being 1) the immunosuppressive microenvironment that leads to T cell exhaustion and 2) loss of antigen and/or checkpoint ligand expression on tumour cells rendering the tumour unrecognisable by T cells. Importantly, there may be additional, undiscovered immune evasion mechanisms that could be exploited for immunotherapy.
Dr Zeissig’s lab is focused on understanding how cancers evade the immune system to identify new ways to enhance response to immunotherapy. In particular, her team work on lung and pancreatic cancers driven by mutations in the cancer gene KRAS. They utilise a range of tools including genetically engineered preclinical models of cancer, analysis of immune cell subsets, single-cell profiling and molecular biology techniques. They also harness large-scale genetic screening using CRISPR-Cas9 technology to find previously unknown targets and mechanisms that regulate response to immunotherapy.
Source: Supplied
https://orcid.org/0000-0003-3264-6546
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Health and economic burden of interstitial lung diseases
Dr Cox’s main research interests focus on respiratory diseases and primarily on the economic burden and economic evaluation of interventions and treatments for their management. She earned her PhD from the University of Tasmania where her doctoral research examined the health and economic burden of idiopathic pulmonary fibrosis (IPF) in Australia, one component of the NHMRC Centre for Research Excellence for Pulmonary Fibrosis, a national project implemented alongside the Australian IPF Registry and the Lung Foundation Australia. This research provided the first epidemiological profile and first costing estimates of the economic burden of the disease in Australia, providing essential evidence for health service reimbursement policies.
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Professor Tim Hughes is an international expert in the biology and treatment of leukaemia. He led the establishment of the molecular response criteria that are used world-wide to measure response in chronic myeloid leukaemia (CML) and has led many of the key Global and National trials. His group has successfully developed predictive bioassays and molecular targets that influence the way CML patients are managed world-wide. He has published over 350 papers that have been cited over 65,000 times.
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