Correlation of High-Grade Osteosarcoma Response to Chemotherapy with Enhanced Tissue Immunological Response: Analysis of CD95R, IFN-γ, Catalase, Hsp70, and VEGF.
Sjahjenny MustokoweniFerdiansyah MahyudinRosy SetiawatiDian NugrahennyMohamad HidayatHandono KalimKaryono MintaroemLoeki Enggar FitriPancras C W HogendoornPublished in: Virchows Archiv : an international journal of pathology (2024)
High-grade osteosarcoma, a primary malignant bone tumour, is experiencing a global increase in reported incidence with varied prevalence. Despite advances in management, which include surgery and neoadjuvant chemotherapy often an unsatisfactory outcome is found due to poor or heterogeneous response to chemotherapy. Our study delved into chemotherapy responses in osteosarcoma patients and associated molecular expressions, focusing on CD95 receptor (CD95R), interferon (IFN)-γ, catalase, heat-shock protein (Hsp)70, and vascular endothelial growth factor (VEGF). Employing immunohistochemistry and Huvos grading of post-chemo specimens, we analysed formalin-fixed paraffin-embedded (FFPE) osteosarcoma tissue of resected post-chemotherapy specimens from Dr. Soetomo General Academic Hospital in Surabaya, Indonesia (DSGAH), spanning from 2016 to 2020. Results revealed varied responses (poor 40.38%, moderate 48.08%, good 11.54%) and distinct patterns in CD95R, IFN-γ, catalase, Hsp70, and VEGF expression. Significant differences among response groups were observed in CD95R and IFN-γ expression in tumour-infiltrating lymphocytes. The trend of diminishing CD95R expression from poor to good responses, accompanied by an increase in IFN-γ, implied a reduction in the count of viable osteosarcoma cells with the progression of Huvos grading. Catalase expression in osteosarcoma cells was consistently elevated in the poor response group, while Hsp70 expression was highest. VEGF expression in macrophages was significantly higher in the good response group. In conclusion, this study enhances our understanding of immune-chemotherapy interactions in osteosarcoma and identifies potential biomarkers for targeted interventions.
Keyphrases
- heat shock protein
- vascular endothelial growth factor
- poor prognosis
- locally advanced
- high grade
- neoadjuvant chemotherapy
- dendritic cells
- endothelial cells
- binding protein
- immune response
- heat shock
- induced apoptosis
- lymph node
- nk cells
- radiation therapy
- physical activity
- risk factors
- low grade
- rectal cancer
- heat stress
- squamous cell carcinoma
- signaling pathway
- gene expression
- ejection fraction
- cell death
- oxidative stress
- endoplasmic reticulum stress
- prognostic factors
- high intensity
- acute coronary syndrome
- long non coding rna
- single cell
- chemotherapy induced
- combination therapy