Explainable Generative AI Uncovers a Molecular Continuum in Medulloblastoma with Implications for Rare Cancer Subtyping and Treatment Equity
Prol-Castelo, G.; Tejada-Lapuerta, A.; Urda-Garcia, B.; Nunez-Carpintero, I.; Garcia-Verellen, E.; Montagud, A.; Valencia, A.; Cirillo, D.
Show abstract
Medulloblastoma is a childhood brain tumor traditionally classified into four molecular subgroups. Recent evidence suggests that Groups 3 and 4 represent a biological continuum rather than distinct entities, a paradigm shift with significant implications for understanding disease biology and treatment strategies. Nevertheless, assessing this hypothesis is challenging mainly due to data scarcity. In this study, we analyze the largest available transcriptomics dataset to provide compelling evidence for the existence of an intermediate subgroup between Groups 3 and 4, characterized by distinct molecular features. To overcome limitations posed by data scarcity, we employ synthetic data generation using a Variational Autoencoder and apply explainability techniques to identify key relationships between gene expression and disease subgroups. Furthermore, by incorporating Machine Learning Fairness approaches, we demonstrate that overlooking this intermediate subgroup can result in treatment disparities. Our findings are further supported by both existing and newly proposed studies using diverse datasets and methodologies, including graphbased analyses and multi-scale simulations, underscoring the robustness and reproducibility of our results. This study demonstrates the potential of synthetic data generation to refine rare disease subtyping and advance our understanding of the underlying biological mechanisms. Keywords: Medulloblastoma, pediatric cancer, representation learning, autoencoder, synthetic data
Matching journals
The top 8 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- Molecular phenotyping using networks, diffusion, and topology: soft tissue sarcoma 92%
- Interpretable deep recommender system model for prediction of kinase inhibitor efficacy across cancer cell lines 91%
- Unsupervised generative and graph representation learning for modelling cell differentiation 91%
Similar papers in this journal
- Automatic computational classification of bone marrow cells for B cell pediatric leukemia using UMAP 90%
- A Regularized Cox Hierarchical Model for Incorporating Annotation Information in Predictive Omic Studies 90%
- Expanding a Database-derived Biomedical Knowledge Graph via Multi-relation Extraction from Biomedical Abstracts 88%
Similar papers in this journal
- The shape of gene expression distributions matter: how incorporating distribution shape improves the interpretation of cancer transcriptomic data 91%
- De novo identification of maximally deregulated subnetworks based on multi-omics data with DeRegNet 90%
- Ranking Cancer Drivers via Betweenness-based Outlier Detection and Random Walks 90%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.