Moran-Segura, C. | Search bioRxiv

bioRxiv2024

Utility of cellular imaging modality in subcellular spatial transcriptomic profiling of tumor tissues

Spatial transcriptomics (ST) technologies, like GeoMx Digital Spatial Profiler, are increasingly utilized to reveal the role of diverse tumor microenvironment components, particularly in relation to cancer progression, treatment response, and therapeutic resistance. However, in many ST studies, the spatial information obtained from immunofluorescence imaging is primarily used for identifying regions of interest, rather than as an integral part of downstream transcriptomic data interpretation. We developed ROICellTrack, a deep learning-based framework, to better integrate cellular imaging with spatial transcriptomic profiling. By examining 56 ROIs from urothelial carcinoma of the bladder (UCB) and upper tract urothelial carcinoma (UTUC), ROICellTrack accurately identified cancer-immune mixtures and associated cellular morphological features. This approach also revealed different sets of spatial clustering patterns and receptor-ligand interactions. Our findings underscore the importance of combining imaging and transcriptomics for comprehensive spatial omics analysis, offering potential new insights into within-sample heterogeneity and implications for targeted therapies and personalized medicine.

bioinformatics↗

bioRxiv2021

Spatial Clustering of CD68+ Tumor Associated Macrophages with Tumor Cells is Associated with Worse Overall Survival in Metastatic Clear Cell Renal Cell Carcinoma

Immune infiltration is typically quantified using cellular density, not accounting for cellular clustering. Tumor-associated macrophages (TAM) activate oncogenic signaling through paracrine interactions with tumor cells, which may be better reflected by local cellular clustering than global density metrics. Using multiplex immunohistochemistry and digital pathologic analysis we quantified cellular density and cellular clustering for myeloid cell markers in 129 regions of interest from 55 samples from 35 patients with metastatic ccRCC. CD68+ cells were found to be clustered with tumor cells and dispersed from stromal cells, while CD163+ and CD206+ cells were found to be clustered with stromal cells and dispersed from tumor cells. CD68+ density was not associated with OS, while high tumor/CD68+ cell clustering was associated with significantly worse OS. These novel findings would not have been identified if immune infiltrate was assessed using cellular density alone, highlighting the importance of including spatial analysis in studies of immune cell infiltration of tumors. SIGNIFICANCEIncreased clustering of CD68+ TAMs and tumor cells was associated with worse overall survival for patients with metastatic ccRCC. This effect would not have been identified if immune infiltrate was assessed using cell density alone, highlighting the importance of including spatial analysis in studies of immune cell infiltration of tumors.

cancer biology↗