STC2-mediated calcium homeostasis dysregulation in the osteosarcoma microenvironment: Insights from single-cell...

Osteosarcoma (OS) is an aggressive bone malignancy with a poor prognosis. Dysregulated calcium homeostasis may contribute to OS progression.

Various machine learning algorithms were integrated into multiple model combinations to identify key prognostic genes. Single-cell expression profiling was conducted to assess STC2 expression across different cell types within the OS microenvironment. Experimental validation was performed in OS cell lines (U2OS and 143B) using lentiviral shRNA-mediated knockdown, qPCR, proliferation assays, and migration/invasion assays. Immune infiltration and potential immunotherapy response were further explored using immune deconvolution, immune checkpoint analysis, TIDE, and SubMap.

Calcium homeostasis-related dysregulation was associated with osteosarcoma progression, and machine-learning analysis identified STC2 as the most important prognostic gene. Single-cell analysis revealed that STC2 was predominantly expressed in endothelial, fibroblast, and malignant cells. In vitro experiments showed that knockdown of STC2 in OS cells significantly inhibited cell proliferation, migration, and invasion. Specifically, CCK-8, colony formation, and EdU assays demonstrated decreased cell proliferation, while Transwell assays revealed reduced migratory and invasive capacities of STC2-knockdown OS cells. Moreover, TIDE and SubMap analyses suggested that low STC2 expression was computationally associated with a higher predicted likelihood of response to immune checkpoint inhibitors.

Our findings suggest that calcium homeostasis dysregulation is involved in OS progression and that STC2 is a prioritized prognostic and functional candidate within this network. The findings suggest that STC2 may serve as a potential therapeutic target and candidate biomarker for OS, including in the context of predicted immunotherapy response, although this requires further validation.