NCI Data Jamboree (Project Abstract Submission): Submission #19
Submission information
Submission Number: 19
Submission ID: 186660
Submission UUID: 33ff26ab-39bc-4ca9-904f-5452695e4649
Submission URI: /nci/datajamboree/abstractsubmission
Submission Update: /nci/datajamboree/abstractsubmission?token=DP5gIU6WENai2NJ6QRNCslgGRPhCDpRoMeZeKBkUvbE
Created: Wed, 07/15/2026 - 12:10
Completed: Wed, 07/15/2026 - 14:14
Changed: Wed, 07/15/2026 - 14:14
Remote IP address: 10.208.24.175
Submitted by: Anonymous
Language: English
Is draft: No
Webform: NCI Data Jamboree (Abstracts)
Submitted to: NCI Data Jamboree (Project Abstract Submission)
Presenter Information
Additional Authors
Abstract Information
Employing statistical, computational, and informatics tools, algorithms, and methods to integrate or analyze data
Prostate cancer, proteomics, glycoproteomics, phosphoproteomics, crosstalk
Unlocks the Biological Insights into Aggressive Prostate Cancer Using Multi-omic Approach
Scientific Questions: This project integrates large-scale multi-omics to address: (1) how multi-layer genomics, proteomics (TMT/DIA), and post-translational modifications (PTMs) correlate globally; (2) how to digitally deconvolve tumor microenvironment (TME) cell fractions; and (3) how to map the causal directional regulatory cascades between cell-surface glycosylation and intracellular phosphorylation to identify therapeutic targets.
Community Significance: Prostate cancer has profound molecular heterogeneity. Providing a reproducible, open-source computational framework for integrating mass-spectrometry-based proteomics and dual-PTM networks allows the broader cancer research community to uncover targetable biological pathways and patient subclusters obscured in genomic-only studies.
Datasets & Tools: We leverage clinical cohorts (244 samples) with comprehensive transcriptomics, global proteomics (TMT/DIA), and deeply enriched PTMs (phospho, intact glycopeptide, ubiquitin, p-Tyr, acetyl). Key informatics tools include xCell/CIBERSORTx for cellular deconvolution, Random Forest and Lasso-logistic regression for tumor grading classifiers (NAT vs. Low/High Gleason grades), human interactome mapping for protein-protein interaction (PPI) topology, and Bayesian modeling for causal dual-PTM network inference.
Community Significance: Prostate cancer has profound molecular heterogeneity. Providing a reproducible, open-source computational framework for integrating mass-spectrometry-based proteomics and dual-PTM networks allows the broader cancer research community to uncover targetable biological pathways and patient subclusters obscured in genomic-only studies.
Datasets & Tools: We leverage clinical cohorts (244 samples) with comprehensive transcriptomics, global proteomics (TMT/DIA), and deeply enriched PTMs (phospho, intact glycopeptide, ubiquitin, p-Tyr, acetyl). Key informatics tools include xCell/CIBERSORTx for cellular deconvolution, Random Forest and Lasso-logistic regression for tumor grading classifiers (NAT vs. Low/High Gleason grades), human interactome mapping for protein-protein interaction (PPI) topology, and Bayesian modeling for causal dual-PTM network inference.