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Evaluation of the Efficacy of the H. pylori Protein HP-NAP as a Therapeutic Tool for Treatment of Bladder Cancer in an Orthotopic Murine Model
Published on: May 29, 2015
Integrative Deep Learning from H&E Images Reveals Prognostically Distinct Pathology-Based Subtypes in Bladder Cancer
Huanhui Li1, Fazhong Dai1, Yongqiang Zhang1,2
1Department of Urology, The Affiliated Guangdong Second Provincial General Hospital of Jinan University, Guangzhou 510317, China.
Background:
Molecular subtyping guides bladder cancer (BCa) care but typically requires RNA profiling. This study aimed to develop pathology-based subtypes of BCa using pathology deep learning features derived from routinely obtained hematoxylin and eosin (H&E)-stained whole-slide images (WSIs).
Methods:
We developed a pathology-based subtype of BCa based on deep learning features extracted from H&E-stained WSIs. A modified Resnet50 model was trained to distinguish between tumor and normal regions and extract patch-level deep learning features. These features were aggregated at the WSI level, followed by weighted gene co-expression network analysis (WGCNA), Cox regression, and unsupervised K-means clustering to define pathology-based subtypes. External validation was performed using WSIs from four independent centers and transcriptomic data from IMvigor210 and GSE32894 cohorts. Interpretability used Grad-CAM on tumor patches.
Results And Discussion:
The Resnet50 model achieved high and consistent performance in distinguishing tumor and normal patches. The analysis identified four BCa subtypes, with distinct clinical outcomes. Clusters 2/3 were predominantly luminal-like (cluster 3 was enriched for FGFR3 and had the lowest TMB), whereas clusters 0/1 exhibited mixed luminal/ basal features with higher immune/stromal scores; regulon and pathway profiles diverged (e.g., EGFR/FOXM1/STAT3 in cluster 1 vs. FGFR3/FOXA1/PPARG in cluster 3). Grad-CAM highlighted distinct nuclear morphologies supporting interpretability.
Conclusion:
We present a pathology-based subtype of BCa that is portable, prognostically informative, and mechanistically concordant with RNA-defined biology. The approach offers a cost-effective and accessible alternative to traditional molecular profiling methods, with potential applications in personalized treatment and improved patient stratification.
