Molecular state
Single-cell expression, regulatory activity, mutations, copy-number changes, and pathway programs.
Computational oncology for carcinomas
Pathelium is building Epithelia AI, a multimodal foundation model of epithelial biology. Learning from single-cell, spatial, genomic, pathology, and organoid data, it is being developed to model carcinoma progression and responses to genetic and therapeutic interventions.
Built for cancer researchers, computational biologists, organoid teams, and translational drug discovery.
The biological problem
Carcinomas develop as epithelial cells lose the programs that maintain healthy tissue. These changes may affect cell identity, differentiation, polarity, genomic regulation, tissue organization, and interactions with neighboring cells.
Researchers can observe parts of this process through single-cell sequencing, spatial assays, pathology, organoids, and perturbation experiments. The challenge is connecting these measurements into a predictive model of how epithelial disease changes over time.
Pathelium is building that computational layer.
Epithelia AI
A research platform for learning transferable representations across epithelial cells, tissues, disease states, and interventions.
Epithelia AI is being designed as a multimodal foundation model that can learn reusable representations of epithelial biology across data types and experimental systems.
Describe cell identity, tissue organization, disease context, and heterogeneity.
Generate testable predictions about future states after an intervention.
Conceptual model
The platform is intended to model heterogeneous responses across a cell population—not only an average expression profile.
Conceptual research framework — not a clinical prediction
Possible population outcomes
Multimodal foundation
Epithelia AI is being developed to connect signals measured at different biological scales, from molecular programs inside a cell to tissue architecture and intervention response.
Single-cell expression, regulatory activity, mutations, copy-number changes, and pathway programs.
Tissue neighborhoods, cell-to-cell interactions, architecture, and the local microenvironment.
Histology, organoid imaging, structural organization, dysplasia, and invasion-associated changes.
Genetic alterations, CRISPR interventions, drugs, combinations, doses, and treatment duration.
Cell lines, patient-derived organoids, tissue samples, and longitudinal measurements.
Research applications
These are intended research capabilities under development, not clinically validated tools or treatment recommendations.
Study transitions from healthy epithelium to dysplasia, invasive carcinoma, and treatment-resistant disease.
Estimate how epithelial cells and organoids may respond to genetic alterations, drugs, and drug combinations.
Investigate small or emerging cellular populations associated with treatment persistence and relapse.
Rank candidate interventions and support decisions about which hypotheses to test next.
Study how responses in organoids and other experimental systems may relate to tissue and patient-level outcomes.
Why epithelial biology
Epithelia are not interchangeable surfaces. Each tissue maintains a specialized identity, architecture, and relationship with its environment. A useful model must learn those constraints before it can study how they break down.
Explore the epithelial biologyLineage identity, differentiation, and the barrier and secretory programs that define a healthy epithelium.
Polarity, adhesion, tissue architecture, and the coordinated repair programs that maintain a tissue boundary.
Inflammation, plasticity, dysplasia, invasion, and partial or complete epithelial-to-mesenchymal transition.
Drug tolerance, resistance, and the changing interactions between epithelial, immune, and stromal cells.
Pathelium’s long-term objective is an epithelial virtual cell: a computational model that can represent a baseline epithelial system and simulate how a heterogeneous population may change after a genetic or therapeutic intervention.
This is a research direction rather than a completed capability. Progress depends on carefully linked perturbation data, rigorous evaluation, and experimental validation.
The system should produce
Scientific principles
Connect molecular, spatial, morphological, perturbational, and experimental data.
Generate testable predictions about epithelial state transitions and intervention response.
Relate outputs to genes, pathways, cellular programs, morphology, and possible mechanisms.
Communicate confidence and identify predictions made outside familiar biological contexts.
Evaluate models with held-out data, controlled perturbations, organoid experiments, and eventually prospective studies.
Who Pathelium is for
Research collaboration
We are interested in working with researchers and organizations studying epithelial biology, patient-derived organoids, perturbation response, carcinoma progression, and treatment resistance.
Research updates
Join researchers, clinicians, and biotechnology leaders following Pathelium’s progress in epithelial foundation models and computational oncology.