Towards Trustworthy Biological Alignment in TabPFN-Probed Pathology Foundation Models

Histology and transcriptomics provide complementary views of tissue biology, capturing spatial morphology and molecular activity, respectively. Pathology foundation models (PFMs) learn rich morphological representations from H&E images, yet strong downstream performance alone does not establish whether these representations encode biologically meaningful and robust molecular information. We present a **training-free framework for auditing biological alignment in frozen PFMs** using spatially paired histology and transcriptomics from HEST-1k, evaluated on **240 samples spanning three organs**. Multiple frozen PFMs are used to extract H&E representations, while gene expression is aggregated into biologically interpretable pathway-level programs. We use TabPFN as a pretrained probe to quantify the extent to which these molecular programs can be decoded from frozen image representations without task-specific gradient updates. Beyond predictive performance, our audit examines whether pathway decodability generalizes across tissue sections, patient groups, and tissue types; whether representations exhibit section-level or other shortcut dependencies; and whether predictions remain stable under small image perturbations and context resampling. This multi-tissue evaluation distinguishes molecular programs that are consistently encoded from those that are tissue-specific, unstable, or shortcut-sensitive. Our framework therefore provides a systematic approach for assessing not only **what biological information pathology foundation models encode, but also how reliably that information persists under clinically relevant sources of variation**.