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Biology subjects

Rueda, L.

Publications and source records attributed to Rueda, L..

2 recordsLinked to original sources

Hypergraph Neural Networks Reveal Spatial Domains from Single-cell Transcriptomics Data

I.Spatial transcriptomics enables the measurement of gene expression while preserving spatial context within tissue samples. A key challenge is detecting spatial domains of biologically meaningful cell clusters, typically addressed using graph-based models like SpaGCN and STAGATE. However, these methods only capture pairwise relationships and fail to model complex higher-order interactions. We propose a hypergraph-based framework for spatial transcriptomics using Hypergraph Neural Networks (HGNNs). Our approach constructs hyperedges from top-K densest overlapping subgraphs and integrates histological image features and gene expression profiles. Combined with autoencoders, our model effectively learns expressive node embeddings in an unsupervised setting. Evaluated on a mouse brain dataset, our model achieves the highest iLISI score of 1.843 and outperforms state-of-the-art baselines with an ARI of 0.51 and a Leiden score of 0.60.

bioinformatics↗

A spatiotemporal cancer cell trajectory underlies glioblastoma heterogeneity

Cancer cells display highly heterogeneous and plastic states in glioblastoma, an incurable brain tumour. However, how these malignant states arise and whether they follow defined cellular trajectories across tumours is poorly understood. Here, we generated a deep single cell and spatial multi-omic atlas of human glioblastoma that pairs transcriptomic, epigenomic and genomic profiling of 12 tumours across multiple regions. We identify that glioblastoma heterogeneity is driven by spatially-patterned transitions of cancer cells from developmental-like states towards those defined by a glial injury response and hypoxia. This cellular trajectory regionalises tumours into distinct tissue niches and manifests in a molecularly conserved manner across tumours as well as genetically distinct tumour subclones. Moreover, using a new deep learning framework to map cancer cell states jointly with clones in situ, we show that tumour subclones are finely spatially intermixed through glioblastoma tissue niches. Finally, we show that this cancer cell trajectory is intimately linked to myeloid heterogeneity and unfolds across regionalised myeloid signalling environments. Our findings define a stereotyped trajectory of cancer cells in glioblastoma and unify glioblastoma tumour heterogeneity into a tractable cellular and tissue framework.

cancer biology↗