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Popp, H.D. ; Bohlander, S.K.

Genetic instability in inherited and sporadic leukemias.

Genes Chromosomes Cancer 49, 1071-1081 (2010)
DOI
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Genetic instability due to increased DNA damage and altered DNA repair is of central significance in the initiation and progression of inherited and sporadic human leukemias. Although very rare, some inherited DNA repair insufficiency syndromes (e.g., Fanconi anemia, Bloom's syndrome) have added substantially to our understanding of crucial mechanisms of leukemo-genesis in recent years. Conversely, sporadic leukemias account for the main proportion of leukemias and here DNA damaging reactive oxygen species (ROS) play a central role. Although the exact mechanisms of increased ROS production remain largely unknown and no single pathway has been detected thus far, some oncogenic proteins (e.g., the activated tyrosine kinases BCR-ABLI and FLT3-ITD) seem to play a key role in driving genetic instability by increased ROS generation which influences the disease course (e.g., blast crisis in chronic myeloid leukemia or relapse in FLT3-ITD positive acute myeloid leukemia). Of course other mechanisms, which promote genetic instability in leukemia also exist. A newly emerging mechanism is the genome-wide alteration of epigenetic marks (e.g., hypomethylation of histone H3K79), which promotes chromosomal instability. Taken together genetic instability plays a critical role both in inherited and sporadic leukemias and emerges as a common theme in both inherited and sporadic leukemias. Beyond its theoretical impact, the analysis of genetic instability may lead the way to the development of innovative therapy strategies.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Korrespondenzautor
Schlagwörter Double-strand breaks; Acute Myeloid-leukemia; Chronic myelogenous leukemia; Acute myeloblastic-leukemia; Defending genome integrity; Fusion tyrosine kinases; FLT3 inhibitor PKC412; DNA-Ligase IV; Recombination repair; Oxidative stress
ISSN (print) / ISBN 1045-2257
e-ISSN 1098-2264
Zeitschrift Genes, Chromosomes and Cancer
Quellenangaben Band: 49, Heft: 12, Seiten: 1071-1081 Artikelnummer: , Supplement: ,
Verlag Wiley
Verlagsort Hoboken
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) CCG Pathogenesis of Acute Myeloid Leukemia (KKG-KPL)