期刊
FREE RADICAL BIOLOGY AND MEDICINE
卷 162, 期 -, 页码 -出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2020.11.027
关键词
CREBBP; Quinone; Oxidative metabolite; Inhibition; Zinc-finger cysteines; Histone acetylation
资金
- Universite de Paris
- CNRS
- ANSES (Agence Nationale de Securite Sanitaire de l'Alimentation, de l'Environnement et du Travail)
- ITMO Cancer (plan Cancer-Environnement)
- China Scholarship Council PhD fellowships
- Universite de Paris (ED BioSPC)
The study reveals that etoposide quinone impairs the tumor suppressor gene CREBBP by reacting with cysteine residues, leading to a reduction in hematopoiesis. This irreversible inhibition of CREBBP activity suggests a potential mechanism for therapy-related leukemia caused by etoposide.
Etoposide is an extensively prescribed anticancer drug that, unfortunately, causes therapy-related leukemia. The mechanisms by which etoposide induces secondary hematopoietic malignancies are poorly documented. However, etoposide-related leukemogenesis is known to depend on oxidative metabolites of etoposide, notably etoposide quinone, that can react with protein cysteine residues such as in topoisomerases II. CREBBP is a major histone acetyltransferase that functions mainly as a transcriptional co-activator. This epigenetic enzyme is considered as a tumor suppressor that plays a major role in hematopoiesis. Genetic alterations affecting CREBBP activity are highly common in hematopoietic malignancies. We report here that CREBBP is impaired by etoposide quinone. Molecular and kinetic analyses show that this inhibition occurs through the rapid and covalent (k(inhib) = 16.10(2) M-1.s(-1)) adduction of etoposide quinone with redox sensitive cysteine residues within the RING and PHD Zn2+-fingers of CREBBP catalytic core leading to subsequent release of Zn2+. In agreement with these findings, experiments conducted in cells and in mice treated with etoposide showed irreversible inhibition of endogenous CREBBP activity and decreased H3K18 and H3K27 acetylation. As shown for topoisomerases II, our work thus suggests that the leukemogenic metabolite etoposide quinone can impair the epigenetic CREBBP acetyltransferase through reaction with redox sensitive cysteine residues.
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