Leveraging untargeted metabolomics in combination with machine learning to uncover novel insights into bladder cancer
Untargeted metabolomics has emerged as a powerful approach to uncover metabolic dysregulation associated with cancer progression. When integrated with a machine learning strategy it facilitates the discovery of key metabolic pathways and predictive biomarkers with high diagnostic and prognostic value. In this study, we employed liquid chromatography coupled to high-resolution Tribrid Orbitrap mass spectrometry to perform comprehensive metabolic profiling of bladder cancer (BLCA) as well as predict invasiveness of the disease. By leveraging both in-house retention time-based MS/MS spectral libraries and commercial databases, we robustly identify over 2000 metabolites. In addition, this platform allows identification of novel pathways highlighting metabolic vulnerabilities in BLCA. The application of machine learning algorithms and advanced computational modeling uncovered metabolic signatures that differentiate BLCA from adjacent normal/benign samples and distinguish muscle-invasive from non-muscle-invasive bladder cancer. Our integrative analytical pipeline addresses key challenges in metabolomics-including high dimensionality, metabolite annotation, and biological variability-through feature selection and predictive modeling. We identify candidate metabolic markers with strong potential for early detection and characterize invasiveness of the disease and identify potential therapeutic target pathways. This work highlights the power of combining untargeted metabolomics with machine learning to map the metabolic landscape of BLCA and to accelerate the development of precision diagnostics and future therapeutic strategies.
Authors
- Krishna Parsawar (ORCID: https://orcid.org/0009-0001-2325-7621)
- Tanmay Gandhi (ORCID: https://orcid.org/0000-0002-5530-7558)
- Vasanta Putluri (ORCID: https://orcid.org/0000-0001-7943-2209)
- Arun Sreekumar (ORCID: https://orcid.org/0000-0003-1582-3774)
- Lívia S. Eberlin (ORCID: https://orcid.org/0000-0002-3885-3215)
- Subrata Sen (ORCID: https://orcid.org/0000-0001-6884-6246)
- Chris A. Beecher
- Sachin B. Jorvekar (ORCID: https://orcid.org/0000-0002-8567-9301)
- Cristian Coarfa (ORCID: https://orcid.org/0000-0002-4183-4939)
- Sandra L. Grimm (ORCID: https://orcid.org/0000-0002-0682-3134)
- Abu Hena Mostafa Kamal (ORCID: https://orcid.org/0000-0001-6750-0729)
- Karthik Reddy Kami Reddy (ORCID: https://orcid.org/0000-0002-3288-394X)
- Chandra Shekar R. Ambati
- Chandra Sekhar Amara (ORCID: https://orcid.org/0000-0002-8256-7291)
- Amrit Koirala (ORCID: https://orcid.org/0009-0008-6323-6041)
- Yair Lotan
- Nagireddy Putluri
- M. Minhaj Siddiqui
- Seth P. Lerner
- Felice de Jong
- Dexue Fu
- Meredith Lauren Spradlin
Institutions
- University of Maryland, Baltimore (US)
- The University of Texas MD Anderson Cancer Center (US)
- University of Arizona (US)
- Baylor University (US)
- Baylor College of Medicine (US)
- Children's Cancer Center (US)
- The University of Texas Southwestern Medical Center (US)
Publication Details
- Journal
- Cancer & Metabolism
- Published
- 2026-04-01
- DOI
- https://doi.org/10.1186/s40170-026-00427-4
- Citations
- 1
- Primary Topic
- Metabolomics and Mass Spectrometry Studies
- Type
- article
- Field-Weighted Citation Impact
- 11.46
Funders
- U.S. Department of Defense
- Cancer Prevention and Research Institute of Texas
- University of Texas Southwestern Medical Center
- National Institutes of Health
- National Cancer Institute