Pancreatic Ductal Adenocarcinoma is a severe, age-related malignancy characterized by late
diagnosis and poor prognosis. As life expectancy increases, the rising incidence of PDAC
presents a critical challenge to long-term healthy aging. While the exact causes of PDAC
remain complex, emerging evidence suggests that the gut microbiome plays a pivotal role in
modulating systemic inflammation, immune surveillance, and oncogenesis.
This project aims to leverage artificial intelligence to uncover specific gut microbiome
signatures associated with the risk and early pathogenesis of PDAC. By analyzing the largescale, high-resolution shotgun metagenomic data provided by the Dutch Microbiome
Project, we intend to move beyond broad associations and identify robust, predictive
microbial biomarkers that signal early vulnerability to pancreatic oncogenesis.
To achieve this, we will apply advanced machine learning algorithms to the dataset's
complex taxonomic and functional profiles. The computational workflows will be executed
securely on the University of Birmingham's BlueBear high-performance computing
cluster. We will strictly adhere to all required data governance measures, ensuring the files
are held on the institutional compute system with appropriately restricted Unix user group
access, safely behind a secure firewall, with absolutely no Unix world read/write access
permitted.
Ultimately, this research seeks to translate massive biological datasets into actionable
oncological insights. By pinpointing the precise microbial drivers or early indicators of PDAC,
we aim to contribute to the development of non-invasive, early-detection strategies.
Identifying these signatures is a crucial step toward proactive cancer prevention, directly
supporting the broader clinical goal of promoting healthy aging and extending disease-free
life expectancy.
Identifying Gut Microbiome Signatures of Pancreatic Ductal Adenocarcinoma (PDAC) Risk to Promote Healthy Aging in population
Year of approval
2026
Institute
University of Birmingham (UK)
Primary applicant
Shirley, M.