Undifferentiated spindle cell sarcoma (UDS) is a poorly defined or understood entity, essentially a waste-basket for cases failing to fulfill criteria for better-established diagnoses based on combined histology, immunohistochemistry, and tumor genetic assays. We identified a novel chromosomal translocation t(17;19)(p13;q13) in a pediatric UDS and have characterized this alteration to show rearrangement of the MLL4 and GPS2 genes, resulting in an in-frame fusion gene MLL4-GPS2, the expression of which promotes anchorage-independent growth. MLL4 was previously reported to be similarly rearranged in hepatocellular carcinomas, notably those positive for hepatitis B virus. Isolated reports of individual rearrangements of GPS2 in a prostate carc...
ABSTRACT Pediatric Ewing sarcoma is characterized by the expression of chimeric fusions of EWS and E...
Infantile fibrosarcomas (IFS) represent a distinct group of soft tissue tumors occurring in patients...
International audienceRhabdomyosarcomas with TFCP2 fusions represent an emerging subtype of tumors, ...
Undifferentiated spindle cell sarcoma (UDS) is a poorly defined or understood entity, essentially a ...
Item does not contain fulltextAn increasing number of congenital and infantile sarcomas displaying a...
Sclerosing rhabdomyosarcoma (ScRMS) and spindle cell rhabdomyosarcoma (SRMS) have been recently recl...
Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children and adolescents. Alveolar ...
A novel group of S100- and CD34-positive spindle cell tumors with distinctive stromal and perivascul...
Chromosomal rearrangements involving the mixed‐lineage leukemia (MLL1) gene are common in a unique g...
Paediatric undifferentiated soft tissue sarcomas (USTSs) are a diagnostically challenging group of n...
A subset of human sarcomas including malignant fibrous histiocytoma and liposarcoma have been found ...
Chromosomal rearrangements of the MLL gene are uncommon in myelodysplastic syndromes (MDSs), and few...
Soft tissue tumors can be categorized molecularly into two categories: tumors which are known to hav...
grantor: University of TorontoAn understanding of the genetic changes that lead to maligna...
MLL is a promiscuous gene involved in a diversity of chromosomal fusions in haematological malignanc...
ABSTRACT Pediatric Ewing sarcoma is characterized by the expression of chimeric fusions of EWS and E...
Infantile fibrosarcomas (IFS) represent a distinct group of soft tissue tumors occurring in patients...
International audienceRhabdomyosarcomas with TFCP2 fusions represent an emerging subtype of tumors, ...
Undifferentiated spindle cell sarcoma (UDS) is a poorly defined or understood entity, essentially a ...
Item does not contain fulltextAn increasing number of congenital and infantile sarcomas displaying a...
Sclerosing rhabdomyosarcoma (ScRMS) and spindle cell rhabdomyosarcoma (SRMS) have been recently recl...
Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children and adolescents. Alveolar ...
A novel group of S100- and CD34-positive spindle cell tumors with distinctive stromal and perivascul...
Chromosomal rearrangements involving the mixed‐lineage leukemia (MLL1) gene are common in a unique g...
Paediatric undifferentiated soft tissue sarcomas (USTSs) are a diagnostically challenging group of n...
A subset of human sarcomas including malignant fibrous histiocytoma and liposarcoma have been found ...
Chromosomal rearrangements of the MLL gene are uncommon in myelodysplastic syndromes (MDSs), and few...
Soft tissue tumors can be categorized molecularly into two categories: tumors which are known to hav...
grantor: University of TorontoAn understanding of the genetic changes that lead to maligna...
MLL is a promiscuous gene involved in a diversity of chromosomal fusions in haematological malignanc...
ABSTRACT Pediatric Ewing sarcoma is characterized by the expression of chimeric fusions of EWS and E...
Infantile fibrosarcomas (IFS) represent a distinct group of soft tissue tumors occurring in patients...
International audienceRhabdomyosarcomas with TFCP2 fusions represent an emerging subtype of tumors, ...