Computational oncology for carcinomas

A new model of carcinoma biology

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

Cancer begins with changes we do not yet fully understand

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.

Measured in partsIntegrated over time
Cell stateTissue formGenomeEnvironment

Epithelia AI

A research platform for learning transferable representations across epithelial cells, tissues, disease states, and interventions.

Building a model of epithelial cancer biology

Epithelia AI is being designed as a multimodal foundation model that can learn reusable representations of epithelial biology across data types and experimental systems.

Represent

What state is the system in?

Describe cell identity, tissue organization, disease context, and heterogeneity.

Predict

How might that state change?

Generate testable predictions about future states after an intervention.

Conceptual model

From a biological state to what may happen next

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

1Baseline epithelial state
2Tissue and disease context
3Genetic or therapeutic intervention
ModelEpithelia AI
OutputPredicted distribution of future epithelial states

Possible population outcomes

Cell deathContinued proliferationDifferentiationDrug-tolerant persistenceResistanceMore invasive states

Multimodal foundation

Learning across the biology of a tissue

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.

01

Molecular state

Single-cell expression, regulatory activity, mutations, copy-number changes, and pathway programs.

02

Spatial context

Tissue neighborhoods, cell-to-cell interactions, architecture, and the local microenvironment.

03

Pathology and morphology

Histology, organoid imaging, structural organization, dysplasia, and invasion-associated changes.

04

Perturbation biology

Genetic alterations, CRISPR interventions, drugs, combinations, doses, and treatment duration.

05

Experimental systems

Cell lines, patient-derived organoids, tissue samples, and longitudinal measurements.

Research applications

What researchers could understand earlier

These are intended research capabilities under development, not clinically validated tools or treatment recommendations.

01

Model disease progression

Study transitions from healthy epithelium to dysplasia, invasive carcinoma, and treatment-resistant disease.

02

Predict perturbation response

Estimate how epithelial cells and organoids may respond to genetic alterations, drugs, and drug combinations.

03

Reveal resistant states

Investigate small or emerging cellular populations associated with treatment persistence and relapse.

04

Prioritize experiments

Rank candidate interventions and support decisions about which hypotheses to test next.

05

Connect models to patients

Study how responses in organoids and other experimental systems may relate to tissue and patient-level outcomes.

Why epithelial biology

Built around the cells where carcinomas begin

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 biology

Identity and function

Lineage identity, differentiation, and the barrier and secretory programs that define a healthy epithelium.

  • Lineage
  • Differentiation
  • Barrier function
  • Secretion

Structure and repair

Polarity, adhesion, tissue architecture, and the coordinated repair programs that maintain a tissue boundary.

  • Polarity
  • Cell adhesion
  • Architecture
  • Wound repair

Disease transitions

Inflammation, plasticity, dysplasia, invasion, and partial or complete epithelial-to-mesenchymal transition.

  • Inflammation
  • Plasticity
  • Dysplasia
  • EMT

Response ecology

Drug tolerance, resistance, and the changing interactions between epithelial, immune, and stromal cells.

  • Persistence
  • Resistance
  • Immune context
  • Stroma
Long-term research direction

Toward a virtual model of epithelial response

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

  1. 1Testable predictions
  2. 2Population-level response distributions
  3. 3Mechanistic hypotheses
  4. 4Uncertainty estimates
  5. 5Suggested validation experiments

Scientific principles

Built for prediction, interpretation, and validation

01

Multimodal

Connect molecular, spatial, morphological, perturbational, and experimental data.

02

Predictive

Generate testable predictions about epithelial state transitions and intervention response.

03

Interpretable

Relate outputs to genes, pathways, cellular programs, morphology, and possible mechanisms.

04

Uncertainty-aware

Communicate confidence and identify predictions made outside familiar biological contexts.

05

Experimentally grounded

Evaluate models with held-out data, controlled perturbations, organoid experiments, and eventually prospective studies.

Who Pathelium is for

Built with cancer researchers in mind

  • Cancer biology laboratories
  • Organoid research groups
  • Computational biology teams
  • Translational oncology programs
  • Biotechnology companies
  • Pharmaceutical discovery teams

Research collaboration

Help build a better model of epithelial cancer

We are interested in working with researchers and organizations studying epithelial biology, patient-derived organoids, perturbation response, carcinoma progression, and treatment resistance.

Research updates

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