XL t(11;19) KMT2A/MLLT1 DF
XL t(11;19) KMT2A/MLLT1 DF consists of a green-labeled probe hybridizing to the KMT2A gene region at 11q23.3 and an orange-labeled probe hybridizing to the MLLT1 gene region at 19p13.3.
Chromosomal rearrangements of the KMT2A (lysine methyltransferase 2A) gene, formerly MLL (mixed lineage leukemia), are associated with various hematological disorders. Most patients suffer from acute myeloid leukemia (AML) or acute lymphoblastic leukemia (ALL), while only a minority develops mixed lineage leukemia (MLL). Several chromosomal aberrations involving the KMT2A gene have been identified. However, the majority of leukemias result from translocations leading to KMT2A fusions. More than 90 KMT2A translocation partner genes fused to the 5´- KMT2A portion have been identified. The most common translocation partners in KMT2A associated leukemia are AFF1, MLLT3, MLLT1, MLLT10, ELL and AFDN, described here in the order of their frequency. MLLT1 (MLLT1 super elongation complex subunit), originally designated as ENL, is one of the most common KMT2A fusion partners. KMT2A-MLLT1 fusions result from translocations of the type t(11;19)(q23;p13.3). Most patients carrying a KMT2A-MLLT1 fusion have breakpoints in intron 11 of the KMT2A gene. KMT2A-MLLT1 fusions are prevalent in both AML and ALL. Multiple KMT2A translocation partner genes, including MLLT1, are organized within the DOT1L transcriptional complex. AFF1 serves as DOT1L complex docking platform for MLLT1 and MLLT3, while MLLT10 directly mediates this interaction. More precisely, the MLLT1 protein has been shown to interact with AFF1 via its C-terminus. Due to the close interaction of these KMT2A fusion partners with DOT1L, DOT1L inhibitors are considered as promising candidates for treatment of such leukemia cases.
Cena za kus: pro registrované
Chromosomal rearrangements of the KMT2A (lysine methyltransferase 2A) gene, formerly MLL (mixed lineage leukemia), are associated with various hematological disorders. Most patients suffer from acute myeloid leukemia (AML) or acute lymphoblastic leukemia (ALL), while only a minority develops mixed lineage leukemia (MLL). Several chromosomal aberrations involving the KMT2A gene have been identified. However, the majority of leukemias result from translocations leading to KMT2A fusions. More than 90 KMT2A translocation partner genes fused to the 5´- KMT2A portion have been identified. The most common translocation partners in KMT2A associated leukemia are AFF1, MLLT3, MLLT1, MLLT10, ELL and AFDN, described here in the order of their frequency. MLLT1 (MLLT1 super elongation complex subunit), originally designated as ENL, is one of the most common KMT2A fusion partners. KMT2A-MLLT1 fusions result from translocations of the type t(11;19)(q23;p13.3). Most patients carrying a KMT2A-MLLT1 fusion have breakpoints in intron 11 of the KMT2A gene. KMT2A-MLLT1 fusions are prevalent in both AML and ALL. Multiple KMT2A translocation partner genes, including MLLT1, are organized within the DOT1L transcriptional complex. AFF1 serves as DOT1L complex docking platform for MLLT1 and MLLT3, while MLLT10 directly mediates this interaction. More precisely, the MLLT1 protein has been shown to interact with AFF1 via its C-terminus. Due to the close interaction of these KMT2A fusion partners with DOT1L, DOT1L inhibitors are considered as promising candidates for treatment of such leukemia cases.
Cena za kus: pro registrované
