» Articles » PMID: 20698812

Prolyl Hydroxylase Domain-containing Protein Inhibitors As Stabilizers of Hypoxia-inducible Factor: Small Molecule-based Therapeutics for Anemia

Overview
Publisher Informa Healthcare
Date 2010 Aug 12
PMID 20698812
Citations 35
Authors
Affiliations
Soon will be listed here.
Abstract

Importance Of The Field: Anemia caused by chronic kidney disease and other chronic diseases or conditions can be managed by the treatment of biologic-based erythropoiesis stimulating agents (ESAs). Although these ESAs are successful in treating these anemic conditions, a small molecule-based anti-anemia medicine can potentially revolutionize the treatment of anemia by bringing convenience to patients and being cost effective. Prolyl hydroxylase domain-containing protein (PHD) inhibitors may provide an opportunity for the development of small molecule anti-anemia medicines.

Areas Covered In This Review: This review covers efforts to target PHD enzymes for stabilization of hypoxia-inducible factor (HIF)-alpha subunits under normal oxygen levels as an attractive strategy to upregulate the expression of erythropoietin and genes involved in iron metabolism for the treatment of anemia.

What The Reader Will Gain: The reader will gain a brief summary of recent advances in HIF and PHD biology and a review of patents/patent applications on the subject of PHD inhibitors as HIF stabilizers for the treatment of anemia.

Take Home Message: Several classes of PHD enzyme inhibitors have been disclosed and several are currently in clinical trials for the development of small molecule-based therapeutics for the treatment of anemia.

Citing Articles

Pharmacokinetic Study of Vadadustat and High-Resolution Mass Spectrometric Characterization of its Novel Metabolites in Equines for the Purpose of Doping Control.

Ishii H, Shibuya M, Kusano K, Sone Y, Kamiya T, Wakuno A Curr Drug Metab. 2022; 23(10):850-865.

PMID: 36017833 DOI: 10.2174/1389200223666220825093945.


The hypoxia-inducible factor prolyl hydroxylase inhibitor FG4592 promotes natriuresis through upregulation of COX2 in the renal medulla.

Guan N, Zhang M, Gong W, Mao X, Yang S, Hao C Hypertens Res. 2022; 45(5):814-823.

PMID: 35304594 DOI: 10.1038/s41440-022-00889-1.


Structure-Based Design of Selective Fat Mass and Obesity Associated Protein (FTO) Inhibitors.

Shishodia S, Demetriades M, Zhang D, Tam N, Maheswaran P, Clunie-OConnor C J Med Chem. 2021; 64(22):16609-16625.

PMID: 34762429 PMC: 8631710. DOI: 10.1021/acs.jmedchem.1c01204.


Targeting the RNA demethylase FTO for cancer therapy.

Zhou L, Xu H, Huang Y, Yang C RSC Chem Biol. 2021; 2(5):1352-1369.

PMID: 34704042 PMC: 8496078. DOI: 10.1039/d1cb00075f.


The NFIB-ERO1A axis promotes breast cancer metastatic colonization of disseminated tumour cells.

Zilli F, Ramos P, Auf der Maur P, Jehanno C, Sethi A, Coissieux M EMBO Mol Med. 2021; 13(4):e13162.

PMID: 33751828 PMC: 8033524. DOI: 10.15252/emmm.202013162.