MOESM2 of Histone 3.3 hotspot mutations in conventional osteosarcomas: a comprehensive clinical and molecular characterization of six H3F3A mutated cases

Additional file 2: Figure S1. Radiological data of H3F3A mutant osteosarcomas. (A) Case 77896: anteroposterior and lateral radiograph of the left wrist. Arrows indicate toward the lesion with permeated growth pattern (moth-eaten) and periosteal reaction. (B) Case 84676: anteroposterior and lateral radiograph (upper panel) with arrows indicating a large soft tissue mass with prominent mineralization and corresponding sagittal T1- and fat-saturated proton-weighted MR image (lower panel) of the right knee. The tumor involves the adjacent epiphyses through the epiphyseal growth plate (arrow). (C) Case 94316: anteroposterior and lateral radiograph (upper panel) and corresponding sagittal T1-weighted MR image (lower panel left) of the right knee. The MR image shows the intact bone cortex in the cranial part of the lesion (white arrows), but cortical disruption with “wrap-around” sign in the caudal part of the lesion. Anteroposterior radiograph (lower panel right) shows the local recurrence in the soft tissue adjacent to the knee joint prosthesis. (D) Case 84712: anteroposterior and lateral radiograph (upper panel) and corresponding axial T1-weighted and sagittal fat-saturated proton-weighted MR image (lower panel) of the right knee. Arrows indicate periosteal reaction and cortical disruption. (E) Case 94314: anteroposterior radiograph (upper panel, left), coronal fat-saturated T1-weighted MR image after administration of gadolinium contrast agent (upper panel, right) and coronal T1-weighted MR image (lower panel, left) of the right hip. Thickened bone cortex (arrow-heads, hypointense fibrous structure) is wrapped by the lesion. Anteroposterior radiograph (lower panel, right) after hip joint replacement

Additional file 5: of MEST mediates the impact of prenatal bisphenol A exposure on long-term body weight development

Figure S4. Summary scheme: results overview and hypothesis indicating the influence of prenatal BPA exposure on MEST methylation and expression that is associated with adipocyte differentiation and overweight development in infant offspring. (PNG 19 kb

Additional file 4: of MEST mediates the impact of prenatal bisphenol A exposure on long-term body weight development

Figure S3. MTT assay: MTT test for cell viability after exposure to BPA and the solvent control EtOH (0.05%), normalized to unexposed control, Student’s t test *p < 0.05, mean ± SD, n = 3. (JPEG 105 kb

Additional file 1: of MEST mediates the impact of prenatal bisphenol A exposure on long-term body weight development

Table S1. Primer for gene expression analysis. Table S2. Mediator model for the association of prenatal BPA exposure with cord blood MEST DNA methylation and expression (according to Fig. 1c). Table S3. Mediator model for the association of prenatal BPA exposure with cord blood MEST DNA methylation and children’s BMI z scores at year 1 (according to Fig. 3a). Table S4. Mediator model for the association of cord blood MEST DNA methylation and children’s BMI z scores at years 1 and 6 (according to Fig. 3b). (DOCX 45 kb