scholarly journals Characterization of INCB00928, a Potent and Selective ALK2 Inhibitor for the Treatment of Anemia

Blood ◽  
2020 ◽  
Vol 136 (Supplement 1) ◽  
pp. 52-52
Author(s):  
Yaoyu Chen ◽  
Matthew C. Stubbs ◽  
Michelle Pusey ◽  
Xiaoming Wen ◽  
Robert J. Collins ◽  
...  

A significant population of patients with myelofibrosis (MF) develop anemia and either require red blood cell (RBC) transfusions or have an inadequate response to the currently available therapies and become transfusion-dependent. In patients with MF, elevated levels of serum hepcidin, a key iron regulatory hormone, is associated with increased dependence on RBC transfusions and reduced overall survival. Elevated hepcidin expression has also been observed to cause severe functional iron deficiency anemia and is central to the pathophysiology of anemia of chronic disease. Thus, to ensure proper maintenance of iron homeostasis, hepcidin levels are tightly regulated. Specifically, the production of hepcidin is controlled by the bone morphogenetic protein (BMP) type I receptor ACVR1, a gene that encodes the serine/threonine kinase ALK2. In preclinical models, knockdown or complete loss of ALK2 decreases hepcidin production resulting in elevated serum iron levels. In this study, we report characterization of INCB00928, a novel small molecule inhibitor of ALK2 for the treatment of anemia. INCB00928 was observed to have subnanomolar activity against ALK2 and selectivity over ALK1 and ALK3 in biochemical enzyme assays. In cell-based profiling studies, INCB00928 inhibited ALK2 potently and selectively over ALK1 and ALK3 as determined by the inhibition of ligand-induced SMAD pathway signaling. Importantly, in both an immortalized human liver cell line as well as primary human hepatocytes, INCB00928 inhibited BMP-induced production of hepcidin with nanomolar activity. INCB00928 was also observed to have suitable absorption, distribution, metabolism, and excretion properties to be dosed in in vivo rodent studies. In tumor- and inflammation-induced mouse models of anemia, INCB00928 improved RBC count, hemoglobin, and hematocrit levels while decreasing hepcidin levels in a dose-dependent manner. Additionally, consistent with the improved symptoms of anemia, pSMAD1/5 inhibition was observed in a dose-dependent manner in liver tissues collected from INCB00928-treated mice. In summary, INCB00928 is a potent, selective, and orally available small molecule inhibitor of ALK2, which significantly reduces the production of hepcidin in human liver cells, primary hepatocytes, and in rodent models of anemia. For the majority of patients with MF, the management of anemia remains an unmet need. The preclinical findings from this study suggest ALK2 kinase inhibition with INCB00928 may be a promising novel treatment to reduce the production of hepcidin and improve MF-related anemia in humans, thus warranting further investigation. Disclosures Chen: Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Stubbs:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Pusey:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Wen:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Collins:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Kapilashrami:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Rupar:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Thekkat:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Lin:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Bowman:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Yang:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Diamond:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Yeleswaram:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Kim:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Koblish:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Chen:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company. Wee:Incyte Corporation: Current Employment, Current equity holder in publicly-traded company.

Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 2470-2470
Author(s):  
Beatriz Herreros ◽  
Shaomeng Wang ◽  
Maria E. Rodriguez ◽  
Margarita Sanchez-Beato ◽  
Elena Domenech ◽  
...  

Abstract Abstract 2470 Introduction: Impaired apoptosis is a hallmark of CLL cells, in association with overexpression of antiapoptotic Bcl-2 family members, including Bcl-2 and Mcl-1. Several compounds and antisense molecules that interfere with the Bcl-2 family have been proposed for the therapy of CLL, and some are already at clinical trials. These studies have shown that high levels of Mcl-1 may explain resistance to some of these compounds. Moreover, Mcl-1 has been related to BCR signaling and prolonged survival of CLL cells, while MCL-1 expression is an adverse prognosis marker. Previous gene expression studies from our laboratory have shown a heterogeneous expression of the different members of the Bcl-2 family, with subsets of cases showing increased expression. TW-37 is a novel Bcl-2 family small molecule inhibitor that derives from the natural compound gossypol and binds to the BH3-binding groove of Bcl-2, Bcl-XL and interestingly also Mcl-1.Therefore, we aimed at studying the sensitivity of primary CLL samples to TW-37. Materials and Methods: Forty-three peripheral blood samples were collected at diagnosis by the Tumor Bank unit at CNIO and processed in order to obtain either peripheral blood mononuclear cells (PBMCs) or purified B cells. Sensitivity to the compound was analyzed by EC50 calculations using the Cell Titer Glo® commercial kit from Promega. Mcl-1 antibody used was purchased from Santa Cruz (S-19). Expression profiling (Agilent microarray) were normalized and preprocessed using GEPAS utility available at http://gepas.bioinfo.cipf.es/. Apoptosis was measured by AnnexinV/ PI staining using flow cytometry. Results: The small molecule Bcl-2 inhibitor TW-37 was tested in a first series of PBMC CLL primary samples. EC50 values in the low nanomolar range (from 32.82 to 753.1 nM) were obtained. CLL cases with 17p loss showed a lower TW-37 sensitivity. When cases with 17p deletions were excluded from the study, there was a tendency of unmutated-CLL cases to be more sensitive to TW-37 (p= 0.07; n=23). TW-37 was tested on a second series of purified B cells and an inverse correlation between Mcl-1 protein levels and response to TW-37 (Pearson= −0.5; n=9) was observed. Consistently with what is known on the mechanism of action of the compound, TW-37 induced apoptosis in sensitive samples in a time and dose dependent manner. Using gene expression analysis, we identified a group of genes with higher expression in TW-37 resistant samples. This group included GADD45B, CXCL17, VAV2 and PKCQ (BCR signaling) and PIK3CB (p100β subunit of PI3K). Conclusion: CLL samples with p53 pathway integrity were sensitive to Bcl-2-family inhibition using the TW-37 compound. This drug induced apoptosis in a time and dose dependent manner. Sensitivity was associated with naive IGHV genes, and higher levels of expression of Mcl-1, a potential biomarker of TW-37 sensitivity. Moreover, resistance to this compound seems to be related to differential expression of a gene signature that includes CXCL17, VAV2 and PKCQ; this signature might reflect the influence of the microenvironment and/or an exacerbated BCR activation. Disclosures: Garcia-Marco: ROCHE: Consultancy, Honoraria, Research Funding.


2020 ◽  
Vol 181 ◽  
pp. 104854
Author(s):  
Kamal U. Saikh ◽  
Elaine M. Morazzani ◽  
Ashley E. Piper ◽  
Russell R. Bakken ◽  
Pamela J. Glass

2006 ◽  
Vol 4 (12) ◽  
pp. 122
Author(s):  
C. Santocanale ◽  
A. Montagnoli ◽  
P. Tenca ◽  
M. Menichincheri ◽  
B. Valsasina ◽  
...  

2004 ◽  
Vol 101 (20) ◽  
pp. 7618-7623 ◽  
Author(s):  
Y. Gao ◽  
J. B. Dickerson ◽  
F. Guo ◽  
J. Zheng ◽  
Y. Zheng

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