@phdthesis{86ec49bb350249b48090e35b0c487cb6,
title = "Interrogating the functional diversity of type I interferons to generate tailored therapies for cancer",
abstract = "Immunotherapies have changed the landscape of cancer treatment. The tumour microenvironment (TME) often dictates response to immunotherapy, whereby a {\textquoteleft}hot{\textquoteright} tumour is more responsive than their {\textquoteleft}cold{\textquoteright} counterparts. However, many patients remain unresponsive to treatment despite having a {\textquoteleft}hot{\textquoteright} tumour. In this thesis, we explored the functional diversity of type I interferons (IFN-I) against cancer. Utilising sequencing technologies, we showed that expression of IFN-I subtypes within the TME identified a third {\textquoteleft}overheated{\textquoteright} category of tumours. Through interrogation of our preclinical models of tumour control versus progression using advanced data analytic pipelines, we identified therapeutic targets that can enhance tumour elimination.",
keywords = "Immunotherapy, type I interferon, tumour microenvironment, tailored therapies, next generation sequencing",
author = "Hannah Newnes",
year = "2023",
doi = "10.26182/sg5x-7w14",
language = "English",
school = "The University of Western Australia",
}