ArXiv TLDR

QuantumXCT: Learning Interaction-Induced State Transformation in Cell-Cell Communication via Quantum Entanglement and Generative Modeling

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2604.02203

Selim Romero, Shreyan Gupta, Robert S. Chapkin, James J. Cai

cs.ETphysics.bio-phphysics.data-anq-bio.GN

TLDR

QuantumXCT uses quantum entanglement and generative modeling to learn cell-cell communication as state transformations, moving beyond static ligand-receptor databases.

Key contributions

  • Introduces QuantumXCT, a hybrid quantum-classical generative framework for cell-cell communication.
  • Learns interaction-induced state transformations by encoding transcriptomes into Hilbert space via quantum circuits.
  • Recovers complex regulatory dependencies and identifies communication hubs without prior biological assumptions.
  • Provides interpretable interaction networks from quantum circuit topology and quantifies interaction influence.

Why it matters

This paper introduces a novel quantum machine learning approach to infer cell-cell communication, addressing a key limitation of current methods. By modeling communication as state transformations, QuantumXCT enables de novo discovery of complex interaction programs. This work opens new avenues for understanding biological systems and applying quantum computing in single-cell biology.

Original Abstract

Inferring cell-cell communication (CCC) from single-cell transcriptomics remains fundamentally limited by reliance on curated ligand-receptor databases, which primarily capture co-expression rather than the system-level effects of signaling on cellular states. Here, we introduce QuantumXCT, a hybrid quantum-classical generative framework that reframes CCC as a problem of learning interaction-induced state transformations between cellular state distributions. By encoding transcriptomic profiles into a high-dimensional Hilbert space, QuantumXCT trains parameterized quantum circuits to learn a unitary transformation that maps a baseline non-interacting cellular state to an interacting state. This approach enables the discovery of communication-driven changes in cellular state distributions without requiring prior biological assumptions. We validate QuantumXCT using both synthetic data with known ground-truth interactions and single-cell RNA-seq data from ovarian cancer-fibroblast co-culture model. The QuantumXCT model accurately recovered complex regulatory dependencies, including feedback structures, and identified dominant communication hubs such as the PDGFB-PDGFRB-STAT3 axis. Importantly, the learned quantum circuit is interpretable: its entangling topology was translated into biologically meaningful interaction networks, while post hoc contribution analysis quantified the relative influence of individual interactions on the observed state transitions. Notably, by shifting CCC inference from static interaction lookup to learning data-driven state transformations, QuantumXCT provides a generative framework for modeling intercellular communication. This work establishes a new paradigm for de novo discovery of communication programs in complex biological systems and highlights the potential of quantum machine learning in the context of single-cell biology.

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