An interpretable, multi-modal framework that integrates histopathological image analysis with multi-omics profiling, leveraging U-Net-based nuclei segmentation, vision-language models (BLIP), biomedical language models (BioGPT), and explainable AI is proposed.
Abstract
Triple-Negative Breast Cancer (TNBC) is characterized by high heterogeneity, poor prognosis, and limited targeted treatment options. Bridging the gap between molecular alterations and histopathological morphology remains a major challenge in precision oncology. We propose an interpretable, multi-modal framework that integrates histopathological image analysis with multi-omics profiling (somatic mutations, DNA methylation, copy number alterations), leveraging U-Net-based nuclei segmentation, vision-language models (BLIP), biomedical language models (BioGPT), and explainable AI (SHAP, LIME). Our framework achieves strong predictive performance (AUC = 0.989) and provides transparent, biologically grounded interpretations by integrating morphological features with genomically prioritized biomarkers. Cross-modal analysis confirms established TNBC drivers and generates novel, testable hypotheses associating specific epigenetic alterations with distinct morphological phenotypes. While causal validation requires future wet-lab experiments, our framework accelerates hypothesis-driven biomarker discovery by integrating complementary data modalities with language-based reasoning, providing a transparent foundation for hypothesis generation and clinical translation.
Breast cancer is biologically heterogeneous, yet conventional clinical decisions rely on static, single-marker proxies (ER, PR, HER2, and Ki-67) that capture only a narrow slice of tumor biology. This mini-review argues that AI-driven multi-omics biomarkers offer a valuable shift toward systems-level, model-derived pro...
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Multibiomarker integration, supported by prospective validation and automated models, represents a promising approach to personalize treatment algorithms in early-stage TNBC, balancing efficacy and toxicity while guiding escalation and de-escalation strategies.
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