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©The Author(s) 2025.
World J Diabetes. Sep 15, 2025; 16(9): 107663
Published online Sep 15, 2025. doi: 10.4239/wjd.v16.i9.107663
Table 2 Top studies utilizing spatial transcriptomics in diabetic kidney disease
Number
Research topic
Application of ST and key issues resolved
Findings
Ref.
1Discovery of disease-specific cell neighborhoods and signaling pathwaysUsed Slide-seqV2 technology to build cell-neighborhood maps and uncovered cell localization patterns and signaling networksRevealed the cell interactions and signaling pathways in diabetic nephropathyMarshall et al[15], Chen et al[16]
2Epithelial-mesenchymal transition and interactions of renal tubular cells in DKDCombined single-cell RNA sequencing with spatial transcriptomics to define the epithelial-mesenchymal transition of renal tubular epithelial cells and their interactionsGained an in-depth understanding of the dynamic changes and mechanisms of renal tubular epithelial cellsWang et al[17]
3Immune cell infiltration patterns in DKDUtilized spatial transcriptomic analysis to observe increases in specific immune cells in glomeruliClarified the role of immune cell infiltration in disease progressionZhang et al[18]
4Fibrosis-related protein biomarkers in DKDConducted spatial proteomic analysis to reveal late-stage fibrosis-related protein biomarkersProvided potential diagnostic and therapeutic biomarkersHu et al[19]
5Molecular mechanisms of renal tubular injury in DKDIntegrated spatial transcriptomic and proteomic analyses to find IL-32 upregulation and its mechanismsUncovered the key role of IL-32 in renal tubular injuryChung et al[20]
6Pathway alterations in DKDCombined ST with multi-omics approaches to identify signaling pathways involved in DKDUncovered spatial alterations in inflammatory and apoptotic signaling pathwaysDelrue and Speeckaert[21]
7Involvement of AEBP1 in DKDSpatial transcriptomic analysis of kidney biopsies from DKD patientsAEBP1 is notably upregulated and associated with fibrosis and inflammationTao et al[22]


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