CarHE (contrastive alignment of gene expression for hematoxylin and eosin images), a multimodal pretraining framework that infers high-dimensional spatial transcriptomic profiles from routine H&E-stained slides, provides a cost-effective and scalable framework for H&E-based spatial inference, supporting further validation toward translational research applications.
Abstract
Spatial transcriptomic analyses provide spatially resolved gene expression data that can provide insights into complex biological processes. However, current spatial transcriptomics approaches remain financially prohibitive and restricted in resolution, scalability, and gene coverage, limiting broader adoption for large-scale studies. Here, we developed CarHE (contrastive alignment of gene expression for hematoxylin and eosin images), a multimodal pretraining framework that infers high-dimensional spatial transcriptomic profiles from routine H&E-stained slides. By using contrastive learning to align cell type-specific transcriptomic information with histological features, CarHE achieved high prediction accuracy across evaluated datasets and spatial transcriptomics platforms. CarHE approximated spatially organized pathological microenvironment features consistent with tertiary lymphoid structure (TLS)-associated regions in breast cancer, lung cancer, melanoma, and clear cell renal cell carcinoma. Additionally, CarHE inferred approximated 3D spatial transcriptomic context from 2D images, providing more informative neighborhood context than 2D visualization. In a cohort of 880 lung cancer patients, CarHE-derived features were associated with disease-free survival and outperformed current approaches. Overall, CarHE provides a cost-effective and scalable framework for H&E-based spatial inference, supporting further validation toward translational research applications.
Spatial transcriptomics (ST) enhances single-cell RNA sequencing by revealing transcript distribution, offering critical insights into heterogeneous diseases such as breast cancer. However, the high cost and lengthy processes of generating high-quality ST data limit clinical application. Recent deep learning methods pr...
X-SPATIO is a spatially compatible computational pipeline designed to directly link hematoxylin and eosin morphology with region-matched mRNA and protein expression, enabling cost-effective inference of spatial biomarker expression and establishing a foundation for biologically grounded discovery and precision oncology...
Vibha R. Rao, Madhumala K. Sadanandappa, C. Black et al.· American Journal of Patholog...· 0 citations
Breast cancer exhibits significant spatial and molecular heterogeneity. Traditional bulk and single-cell transcriptomic analyses struggle to fully reveal the molecular states and microenvironmental differences across distinct tumor regions due to their inability to preserve spatial tissue information. This study propos...
Y. Qiao· Theoretical and Natural Scie...· 0 citations
It is argued that the most credible translational goal is not to infer every transcript from H&E, but to identify biologically coherent spatial states with reproducible morphological correlates that can be validated across independent platforms and cohorts before being mapped across large archival collections.
M. A. Rezania, Haechan Yi, Jae-Il Choi et al.· Cancer research and treatmen...· 0 citations
Predicting gene expression from H&E-stained histology images offers a scalable alternative to costly spatial transcriptomics, yet most existing methods operate at the spot level, where signals from multiple cells are aggregated and critical cellular heterogeneity is obscured. Extending this paradigm to single-cell reso...
Zi-Jun Gao, Chun-Bin Gu, Jin-Xi Xiang et al.· 0 citations
Copy number variations (CNV) are key drivers of cancer progression, yet methods for predicting spatial CNVs directly from haematoxylin and eosin (H&E) images are currently lacking. We introduce HisToSpatialCNV, a multiscale deep-learning framework that integrates histopathological features from H&E-stained images to in...