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Cardamone, A.

Publications and source records attributed to Cardamone, A..

2 recordsLinked to original sources

Assessment of Imaging Mass Cytometry (IMC) as a Tool to Characterize Circulating Tumor Cells (CTCs) in Preclinical Mouse Models

Circulating tumor cells (CTCs), particularly multicellular clusters, are associated with poor prognosis and may provide insight into mechanisms of metastasis and therapy resistance. Unbiased approaches for functionally characterizing CTCs in liquid biopsies are therefore urgently needed. Here, we evaluate multiplex imaging mass cytometry (IMC) for CTC analysis in mice bearing human xenograft tumors. In a single-step workflow, IMC uses metal-conjugated antibodies to simultaneously detect numerous proteins and post-translational modifications in minimally processed, small-volume blood samples collected from the tail vein or heart. Using breast cancer cell lines and a patient-derived xenograft (PDX), we assessed a panel of antibodies, including human-specific markers such as Lamin B1 (LMNB1), to enable cross-species interpretation. Combined with manual review, HALO AI-based cell segmentation was used to identify CTCs and quantify marker expression. This approach enables studies of how genetic and pharmacologic interventions alter the properties of single CTCs and CTC clusters in tumor-bearing mice.

cancer biology↗

Spatial profiling identifies regionally distinct microenvironments and targetable immunosuppressive mechanisms in pediatric osteosarcoma pulmonary metastases.

Osteosarcoma is the most common malignant bone tumor in young patients and remains a significant clinical challenge, particularly in the context of metastatic disease. Despite extensive documentation of genomic alterations in osteosarcoma, studies detailing the immunosuppressive mechanisms within the metastatic osteosarcoma microenvironment are lacking. Our objective was to characterize the spatial transcriptional landscape of metastatic osteosarcoma to reveal these immunosuppressive mechanisms and identify promising therapeutic targets. Here, we performed spatial transcriptional profiling on a cohort of osteosarcoma pulmonary metastases from pediatric patients. We reveal a conserved spatial gene expression pattern resembling a foreign body granuloma, characterized by peripheral inflammatory signaling, fibrocollagenous encapsulation, lymphocyte exclusion, and peritumoral macrophage accumulation. We also show that the intratumoral microenvironment of these lesions lack inflammatory signaling. Additionally, we identified CXCR4 as an actionable immunomodulatory target that bridges both the intratumoral and extratumoral microenvironments and highlights the spatial heterogeneity and complexity of this pathway. Collectively, this study reveals that metastatic osteosarcoma specimens are comprised of multiple regionally distinct immunosuppressive microenvironments.

cancer biology↗