Přestavba chromosomové oblasti 3q26 (MECOM) a její klinický význam u myeloidních malignit.

Title in English Remodeling of chromosome 3q26 (MECOM) and its clinical significance in myeloid malignancies
Authors

ŠMEJKAL Jiří ŠMUHAŘOVÁ P. ONDROUŠKOVÁ Eva BRHELOVÁ Eva KULHÁNKOVÁ O. JEŽÍŠKOVÁ Ivana RÁČIL Zdeněk MAYER Jiří POSPÍŠILOVÁ Šárka JAROŠOVÁ Marie

Year of publication 2019
Type Conference abstract
MU Faculty or unit

Faculty of Medicine

Citation
Description Structural chromosome rearrangements of the 3q26 region are described in 5% of patients with myeloid malignancies. Most often these are AML, MDS, CML. The MECOM gene, which is designated as MDS1 and EV1 complex locus, is involved in chromosomal rearrangements in the 3q26 region. Rebuilding MECOM results in its overexpression, which is associated with a very unfavorable prognosis. AML is most often translocation t (3; 3) or inv inversion (3) and patients with this karyotype change form, according to the WHO classification, a separate, prognostically unfavorable subgroup of AML. Chromosome rearrangements involving MECOM occur in karyotype alone or together with chromosome 7 monosomy. The aim of our work is to present a summary of current scientific knowledge with MECOM gene rearrangements and to demonstrate its clinical significance using case reports.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.

More info