Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia.


Autoria(s): van der Reijden, B.A.; Martinet, D.; Dauwerse, J.G.; Giles, R.H.; Wessels, J.W.; Beverstock, G.C.; Smit, B.; Mühlematter, D.; Jotterand Bellomo, M.; Gabert, J.; Lafage-Pochitaloff, M.; Reiffers, J.; Bilhou-Nabera, C.; van Ommen, G.J.; Hagemeijer, A.; Breuning, M.H.
Data(s)

01/09/1996

Resumo

The pericentric inversion on chromosome 16 [inv(16)(p13q22)] and related t(16;16)(p13;q22) are recurrent aberrations associated with acute myeloid leukemia (AML) M4 Eo. Both abberations result in a fusion of the core binding factor beta (CBFB) and smooth muscle myosin heavy chain gene (MYH11). A selected genomic 6.9-kb BamHl probe detects MYH11 DNA rearrangements in 18 of 19 inv(16)/t(16;16) patients tested using HindIII digested DNA. The rearranged fragments were not detectable after remission in two cases tested, while they were present after relapse in one of these two cases tested.

Identificador

https://serval.unil.ch/notice/serval:BIB_7898ADC0B96B

info:pmid:8751463

pmid:8751463

isiid:A1996VF59800007

Idioma(s)

eng

Fonte

Leukemia1091459-1462

Palavras-Chave #Chromosome Inversion; Chromosomes, Human, Pair 16; DNA, Neoplasm/genetics; Gene Rearrangement; Humans; Leukemia, Myelomonocytic, Acute/genetics; Myosin Heavy Chains/biosynthesis; Myosin Heavy Chains/genetics; Oncogene Proteins, Fusion/biosynthesis; Oncogene Proteins, Fusion/genetics; Translocation, Genetic
Tipo

info:eu-repo/semantics/article

article