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Pediatric sarcomaPediatric sarcomaSarcomas are tumors that originate in muscles, tendons, connective tissues, or bones. There are numerous types of sarcomas, and their nomenclature often reflects their tissue of origin. Tumors arising from the body's soft tissues, such as muscles and connective tissues, are collectively referred to as soft tissue sarcomas. Pediatric soft tissue sarcomas represent a heterogeneous group of malignant tumors that originate from primitive mesenchymal tissue, accounting for approximately 6% of all childhood tumors (rhabdomyosarcomas 3% and other soft tissue sarcomas 3%). Sarcomas commonly have few symptoms, becoming noticeable primarily when they grow into surrounding soft tissues or bones, resulting in pain or a palpable mass. Treatment typically involves surgery, chemotherapy and/or radiotherapy, depending on the tumor type and grade of malignancy. Prognosis varies significantly based on histological subtype, malignancy grade, and tumor size. After surgical intervention without detectable residual disease, the majority of patients can be considered cured. However, the prognosis is much poorer in the presence of metastases, with a very small percentage of patients achieving a cure. The risk of metastasis is highest in the first three years following diagnosis. A rhabdoid tumor of the liver is a rare malignancy that originates in the liver and often metastasizes rapidly to other parts of the body. These tumors predominantly occur in infants and toddlers, with the average age at diagnosis at approximately 15 months. Symptoms may include an abdominal mass or gastrointestinal issues such as abdominal pain. Treatment typically involves surgical resection and chemotherapy. NIH - rhabdoid tumor of the liver Differential abundance analysisThis section presents the disease-specific results of the differential abundance analyses. The analyses are reported for three comparisons: 1) disease vs. all other diseases, 2) disease vs. diseases from the same class, and 3) disease vs. healthy samples. Disease vs All other
Disease vs Class
Disease vs Healthy
Figure 1: In the volcano plot, proteins are plotted based on their fold change (logFC) on the x-axis and the statistical significance of the change (-log10 adjusted p-value) on the y-axis. Proteins considered differentially abundant are highlighted, defined by an adjusted p-value < 0.05 and an absolute logFC > 0.5.
Table 1: The summary table lists the results for all comparisons, sorted by p-value by default. It includes key metrics such as fold change and adjusted p-value, to allow exploration of the most significant proteins for each comparison.
Figure 1: In the volcano plot, proteins are plotted based on their fold change (logFC) on the x-axis and the statistical significance of the change (-log10 adjusted p-value) on the y-axis. Proteins considered differentially abundant are highlighted, defined by an adjusted p-value < 0.05 and an absolute logFC > 0.5.
Table 1: The summary table lists the results for all comparisons, sorted by p-value by default. It includes key metrics such as fold change and adjusted p-value, to allow exploration of the most significant proteins for each comparison.
Figure 1: In the volcano plot, proteins are plotted based on their fold change (logFC) on the x-axis and the statistical significance of the change (-log10 adjusted p-value) on the y-axis. Proteins considered differentially abundant are highlighted, defined by an adjusted p-value < 0.05 and an absolute logFC > 0.5.
Table 1: The summary table lists the results for all comparisons, sorted by p-value by default. It includes key metrics such as fold change and adjusted p-value, to allow exploration of the most significant proteins for each comparison.
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Contact
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The Human Protein Atlas