PedAM
Pediatric Disease Annotations & Medicines
| Disease | sarcoma |
| Phenotype | C0553580|ewing sarcoma |
| Sentences | 6 |
| PubMedID- 24206917 | The first detected fusion genes in sarcoma were found in a patient with ewing sarcoma in 1983. this fusion, which is prevalent in 90% of these patients, forms via translocation between chromosomes 11 and 22, resulting in fusion of the ewing sarcoma breakpoint region 1 (ewsr1) gene to members of the e-twenty six (ets) gene family of transcription factor genes[26]–[28]. |
| PubMedID- 25193511 | Medi-573 potently inhibited in vitro proliferation of sarcoma cell lines, with ewing sarcoma cell lines being the most sensitive. |
| PubMedID- 26236597 | The final tissue diagnosis was small round cell sarcoma most consistent with atypical ewing sarcoma likely arising from the chest wall. |
| PubMedID- 22971270 | Small cell osteosarcoma with ewing sarcoma breakpoint region 1 gene rearrangement detected by interphase fluorescence in situ hybridization. |
| PubMedID- 25989269 | Conversely, the cumulative mortality due to spns was twice as high for osteosarcoma compared with ewing sarcoma survivors at the same point (osteosarcoma: 6.7% vs ewing sarcoma: 3.2%). |
| PubMedID- 24805859 | Bcor-ccnb3 fusion transcripts resulting from an x-chromosomal paracentric inversion were recently identified in a series of unclassifiable soft tissue and bone sarcomas with ewing sarcoma-like morphology. |
Page: 1