用拓扑结构增强空间转录组聚类，提升细胞亚群识别精度。

Spatial transcriptomics clustering is pivotal for identifying cell subpopulations by leveraging spatial location information. While recent graph-based methods modeling cell-cell interactions have improved clustering accuracy, they remain limited in two key aspects: (i) reliance on local aggregation in static graphs often fails to capture robust global topological structures (e.g., loops and voids) and is vulnerable to noisy edges; and (ii) dimensionality reduction techniques frequently neglect spatial coherence, causing physically adjacent spots to be erroneously separated in the latent space. To overcome these challenges, we propose SPHENIC, a Spatial Persistent Homology-Enhanced Neighborhood Integrative Clustering method. Specifically, it explicitly incorporates topology-invariant features into the clustering network to ensure robust representation learning against noise. Furthermore, we design a dual-regularized optimization module that imposes spatial constraints alongside distributional optimization, ensuring that the embedding space preserves the physical proximity of cells. Extensive experiments on 11 benchmark datasets demonstrate that SPHENIC outperforms state-of-the-art methods by 4.19%-9.14%, validating its superiority in characterizing complex tissue architectures.