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dc.contributor.authorChlon, Leon
dc.date.accessioned2017-11-03T11:24:37Z
dc.date.available2017-11-03T11:24:37Z
dc.date.issued2017-11-01
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/268068
dc.description.abstractTumours are highly heterogeneous collections of tissues characterised by a repertoire of heavily mutated and rapidly proliferating cells. Evading immune destruction is a fundamental hallmark of cancer, and elucidating the contextual basis of tumour-infiltrating leukocytes is pivotal for improving immunotherapy initiatives. However, progress in this domain is hindered by an incomplete characterisation of the regulatory mechanisms involved in cancer immunity. Addressing this challenge, this thesis is formulated around a fundamental line of inquiry: how do we quantitatively describe the immune system with respect to tumour heterogeneity? Describing the molecular interactions between cancer cells and the immune system is a fundamental goal of cancer immunology. The first part of this thesis describes a three-stage association study to address this challenge in pancreatic ductal adenocarcinoma (PDAC). Firstly, network-based approaches are used to characterise PDAC on the basis of transcription factor regulators of an oncogenic KRAS signature. Next, gene expression tools are used to resolve the leukocyte subset mixing proportions, stromal contamination, immune checkpoint expression and immune pathway dysregulation from the data. Finally, partial correlations are used to characterise immune features in terms of KRAS master regulator activity. The results are compared across two independent cohorts for consistency. Moving beyond associations, the second part of the dissertation introduces a causal modelling approach to infer directed interactions between signaling pathway activity and immune agency. This is achieved by anchoring the analysis on somatic genomic changes. In particular, copy number profiles, transcriptomic data, image data and a protein-protein interaction network are integrated using graphical modelling approaches to infer directed relationships. Generated models are compared between independent cohorts and orthogonal datasets to evaluate consistency. Finally, proposed mechanisms are cross-referenced against literature examples to test for legitimacy. In summary, this dissertation provides methodological contributions, at the levels of associative and causal inference, for inferring the contextual basis for tumour-specific immune agency.en
dc.description.sponsorshipThis PhD was supported by the Cancer Research UK and Engineering and Physical Sciences Research Council Imaging Centre in Cambridge and Manchester (C197/A16465)
dc.language.isoenen
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectCancer Immunologyen
dc.subjectMachine Learningen
dc.subjectStatistical Modellingen
dc.subjectCausalityen
dc.subjectSystems Biologyen
dc.titleMachine Learning Methods for Cancer Immunologyen
dc.typeThesisen
dc.type.qualificationlevelDoctoral
dc.type.qualificationnameDoctor of Philosophy (PhD)
dc.publisher.institutionUniversity of Cambridgeen
dc.publisher.departmentCancer Research UK Cambridge Instituteen
dc.date.updated2017-11-02T18:54:07Z
dc.identifier.doi10.17863/CAM.14294
dc.publisher.collegePembroke
dc.type.qualificationtitlePhD in Medical Sciences
cam.supervisorMarkowetz, Florian
rioxxterms.freetoread.startdate2018-11-03


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Attribution-NonCommercial-NoDerivatives 4.0 International
Except where otherwise noted, this item's licence is described as Attribution-NonCommercial-NoDerivatives 4.0 International