| Literature DB >> 26031919 |
Shuaiying Cui1, Kim-Chew Lim1, Lihong Shi1, Mary Lee1, Natee Jearawiriyapaisarn1, Greggory Myers1, Andrew Campbell2, David Harro3, Shigeki Iwase4, Raymond C Trievel5, Angela Rivers6, Joseph DeSimone7, Donald Lavelle7, Yogen Saunthararajah8, James Douglas Engel1.
Abstract
Inhibition of lysine-specific demethylase 1 (LSD1) has been shown to induce fetal hemoglobin (HbF) levels in cultured human erythroid cells in vitro. Here we report the in vivo effects of LSD1 inactivation by a selective and more potent inhibitor, RN-1, in a sickle cell disease (SCD) mouse model. Compared with untreated animals, RN-1 administration leads to induced HbF synthesis and to increased frequencies of HbF-positive cells and mature erythrocytes, as well as fewer reticulocytes and sickle cells, in the peripheral blood of treated SCD mice. In keeping with these observations, histologic analyses of the liver and spleen of treated SCD mice verified that they do not exhibit the necrotic lesions that are usually associated with SCD. These data indicate that RN-1 can effectively induce HbF levels in red blood cells and reduce disease pathology in SCD mice, and may therefore offer new therapeutic possibilities for treating SCD.Entities:
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Year: 2015 PMID: 26031919 PMCID: PMC4504950 DOI: 10.1182/blood-2015-02-626259
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113