Publications by authors named "B Alman"

Enchondromas are a common tumor in bone that can occur as multiple lesions in enchondromatosis, which is associated with deformity of the affected bone. These lesions harbor somatic mutations in IDH and driving expression of a mutant Idh1 in Col2 expressing cells in mice causes an enchondromatosis phenotype. Here we compared growth plates from E18.

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Intratumoral heterogeneity is common in cancer, particularly in sarcomas like undifferentiated pleomorphic sarcoma (UPS), where individual cells demonstrate a high degree of cytogenic diversity. Previous studies showed that a small subset of cells within UPS, known as the metastatic clone (MC), as responsible for metastasis. Using a CRISPR-based genomic screen , we identified the COMPASS complex member as a key regulator maintaining the metastatic phenotype of the MC in murine UPS.

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Article Synopsis
  • Enchondromas are bone tumors that can appear in multiple lesions due to a condition called enchondromatosis, which leads to bone deformities and is linked to specific genetic mutations.* -
  • In a study, researchers analyzed growth plates from E18.5 mice with a mutant gene compared to normal ones using advanced techniques like single-cell RNA sequencing and found significant differences in cell populations.* -
  • The study revealed that the mutant gene creates unique cell clusters associated with enchondromas while reducing populations that support normal bone growth, suggesting a shift in chondrocyte subpopulations due to the mutation.*
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Background: Femoral shaft fractures are common injuries in children 2 to 7 years of age, with treatments ranging from casting to flexible intramedullary nails (FIN). Each treatment has unique attributes and outcomes are overall similar. Given equivalent outcomes, we hypothesized that a shared decision-making process, using adaptive conjoint analysis (ACA), can be used to assess individual family situations to determine ultimate treatment choice.

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Unlabelled: The interaction between neoplastic and stromal cells within a tumor mass plays an important role in cancer biology. However, it is challenging to distinguish between tumor and stromal cells in mesenchymal tumors because lineage-specific cell surface markers typically used in other cancers do not distinguish between the different cell subpopulations. Desmoid tumors consist of mesenchymal fibroblast-like cells driven by mutations stabilizing beta-catenin.

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