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Highlights•Introducing ProM: merging marker-based and single-cell RNA-seq deconvolution•ProM excels in simulations and paired single-cell/bulk RNA sequencing•Fibroblast subpopulation heterogeneity in tumor subtypes and lymph nodes•SPP1-high MoMacs correlate with poor urothelial cancer outcomesSummaryInteractions within the tumor microenvironment (TME) significantly influence tumor progression and treatment responses. While single-cell RNA sequencing (scRNA-seq) and spatial genomics facilitate TME exploration, many clinical cohorts are assessed at the bulk tissue level. Integrating scRNA-seq and bulk tissue RNA-seq data through computational deconvolution is essential for obtaining clinically relevant insights. Our method, ProM, enables the examination of major and minor cell types. Through evaluation against existing methods using paired single-cell and bulk RNA sequencing of human urothelial cancer (UC) samples, ProM demonstrates superiority. Application to UC cohorts treated with immune checkpoint inhibitors reveals pre-treatment cellular features associated with poor outcomes, such as elevated SPP1 expression in macrophage/monocytes (MM). Our deconvolution method and paired single-cell and bulk tissue RNA-seq dataset contribute novel insights into TME heterogeneity and resistance to immune checkpoint blockade.Graphical abstract
Wang et al. (Tue,) studied this question.