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UOL

Develop and Validate Blood-Borne Lung Cancer Diagnostic Biomarkers Using Multi-Omics and Interpretable AI

University of Liverpool Institute of Systems, Molecular and Integrative Biology
Self-funded 🎓 Applied Mathematics 🎓 Bioinformatics 🎓 Cancer Biology multi-omics lung cancer metabolomics biomarkers proteomics miRNA network-based modelling time-to-event analysis

Explore blood-borne biomarkers for early lung cancer detection using matched proteomic, miRNA, and metabolomic data. Integrate multi-omics with novel network and survival models to uncover early disease signals.

AI-generated overview

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Why This Research Matters

This research has the potential to revolutionize lung cancer detection by identifying biomarkers detectable years before clinical diagnosis, thus enabling earlier and more effective interventions. The integration of multi-omics data and novel AI-driven methods could significantly improve cancer screening programs and patient survival rates.

Systems Medicine Pharmacometrics Quantitative Systems Pharmacology

Project Description

Project Overview

Lung cancer is the leading cause of cancer-related death worldwide. This project seeks to develop and validate blood-borne diagnostic biomarkers to enable early detection to save lives. A unique cohort has been collected in Liverpool with matched proteomic, miRNA, and metabolomic profiles from plasma samples collected 1–10 years prior to clinical diagnosis. The project will utilize network-based supervised stratification (NBS2) and time-to-event (TTE) analysis to identify molecular networks indicative of early oncogenesis and late-stage disease.

What You Will Do

  • Integrate multi-omics data into consistent analytical frameworks.
  • Identify biomarkers by applying NBS2 and TTE analysis alongside benchmarking with other machine learning techniques.
  • Validate findings using independent UK Biobank Olink proteins and metabolic datasets.

Expected Outcomes

The project will provide novel insights into the molecular underpinnings of lung cancer progression by leveraging a first-of-its-kind multi-omics dataset sampled years before diagnosis. Outcomes include novel biomarker panels for early detection and improved understanding of the disease biology through pathway-based models.

Why This Matters

Early detection of lung cancer is critical to improving survival rates. Blood-based miRNA screening has recently shown promise, and this studentship will complement ongoing CRUK-funded efforts. The project trains doctoral candidates in cutting-edge multi-omics, network modelling, and survival analysis, equipping them with skills sought by the pharmaceutical industry.

How to Apply

Please contact the primary supervisor Dr Tao You for any questions.

Eligibility

UK/Home
EU
International

Supervisor Profile

DT
Dr Tao You
University of Liverpool, Institute of Systems, Molecular and Integrative Biology
595 Citations
10 h-index
Google Scholar

Dr Tao You is a researcher specializing in systems medicine, pharmacometrics, and quantitative systems pharmacology. His focus includes applying computational and mathematical modeling approaches to biomedical data. He holds a position at the University of Liverpool, contributing expertise in multi-omics data integration and network-based analysis for disease understanding.

Key Publications

2006 194 citations
Proteomic analysis of colorectal cancer reveals alterations in metabolic pathways: mechanism of tumorigenesis
2012 107 citations
Combinatorial stresses kill pathogenic Candida species
2014 99 citations
Mechanisms underlying the exquisite sensitivity of Candida albicans to combinatorial cationic and oxidative stress that enhances the potent fungicidal activity of phagocytes
2012 38 citations
A systems biology analysis of long and short-term memories of osmotic stress adaptation in fungi
2018 29 citations
A mathematical model of antibody-dependent cellular cytotoxicity (ADCC)

Research Contributions

Analyzed proteomic changes in colorectal cancer revealing key metabolic pathway alterations involved in tumorigenesis.
Provides insight into cancer mechanisms potentially guiding new therapeutic strategies.
Investigated stress responses in Candida albicans demonstrating sensitivity to combinatorial cationic and oxidative stress enhancing immune cell fungicidal activity.
Improves understanding of fungal pathogen vulnerability to host immune defenses, aiding antifungal research.
Developed systems biology models analyzing osmotic stress adaptation in fungi with implications for cellular memory of stress events.
Advances the field of fungal biology and stress response, potentially impacting biotechnology and medical mycology.
Created mathematical models of antibody-dependent cellular cytotoxicity (ADCC) to characterize immune responses.
Supports drug development and immunotherapy by elucidating immune effector mechanisms.

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