1) Definition of clinically relevant endpoints;
2) Training in evaluating pathology and follow up data
3) Delivery of urinary- based machine learning models based on integrative urinary -omics to guide intervention for PCa;
4) Strategic steps to reach implementation; on the basis of the urinary integrative models
1) -omics data retrieval via a systematic search
2) Data alignment and downstream integration
3) Functional annotation to define PCa-related pathways.
1) Drug re-purposing strategies for previously defined agents based on single -omics
2) Preclinical testing of previously identified drug candidates in cell line and animal models
3) Computational drug screening to identify compounds for pre-clinical testing, including different strategies for computational drug screening to be aligned and compared to define selected drugs based on multi-omics integration
4) Application of machine learning and advanced statistics to ascertain correlations among predicted drugs to order them by importance
1) Cell line characterisation at the proteomics level
2) Preclinical testing of -omics based predicted agents in cell line and animal models
3) Proteomics profiling of drug effects to investigate downstream activators
4) Testing of drug combinations to assess synthetic lethal interactions
1) Develop pipeline for pathomics feature extraction from deep learning models
2) Develop and validate DL based pathomics models for PCa stratification and prediction of progression & recurrence
3) Statistical study of associations between imaging -omics features and proteomics features
1) Standardise magnetic resonance imaging parameters, stability analysis of extracted features
2) Extract radiomics features from deep learning models
3) Develop and validate combined deep learning and radiomics models for pre-biopsy stratification;
4) Develop and validate combined -omics models with a focus on accurately ruling out unnecessary biopsies.
1) Establishment of a data management platform
2) Definition of clinically relevant endpoints focusing on primary diagnosis setting
3) Definition of clinically relevant endpoints focusing on metastatic setting
4) Verification of key pathway components at human tissue specimen
5) validation of protein biomarkers at human PCa tissue via immunohistochemistry
1) Consolidation of omics data in the context of prostate cancer
2) Generation of a network-based molecular prostate cancer model
3) Alignment of drug repurposing methods
4) Computational drug screening to identify compounds for pre-clinical testing
5) Identification of drug combinations addressing synthetic lethal interactions
The PROMOTE project has received funding from the European Union’s Horizon Europe Marie Skłodowska-Curie Actions Doctoral Networks - Industrial Doctorates Programme (HORIZON-MSCA-2023-DN-01) under grant agreement No 101169245.
Funded by the European Union. Views and opinions expressed are however those of the author(s) only and do not necessarily reflect those of the European Union. Neither the European Union nor the granting authority can be held responsible for them.
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