Ovarian high-grade serous carcinoma (HGSC) is an aggressive ovarian cancer with a heterogeneous tumor microenvironment (TME). Advances in single-cell RNA sequencing (scRNA-seq) and spatially-resolved transcriptomics have enabled the study of complex TME. This study explores connections between molecular subtypes described from bulk transcriptomes and spatial domains characterized by distinct gene expression in HGSC and their variability between patients. We explored both intra- and inter-tumor heterogeneity across 2D space and identified differing spatial patterns of gene expression pertaining to immune pathways and vasculature development. Functional characterization of tumor spaces revealed potentially shared cell states across molecular subtypes, while correlation analysis underscored subtype-specific spatial anti-colocalization between spots exhibiting antigen-presenting functions and B cell-mediated immunity. Lastly, we performed spatially-aware cell-cell communication analysis on the spatial samples and identified a molecular subtype specific difference in total signaling activity and heterogeneity in Midikine signaling between the differentiated subtype. Our results suggest that generating multiple tissue slices per patient might be necessary to enable comprehensive characterization of HGSC spatial transcriptomes.
Li et al. (Mon,) studied this question.