Growing concerns about using hypoxia-inducible factor prolyl hydroxylase inhibitors for the treatment of renal anemia

被引:7
|
作者
Nakanishi, Takeshi [1 ,2 ]
Kuragano, Takahiro [1 ]
机构
[1] Hyogo Med Univ, Dept Internal Med, Div Kidney Dialysis & Cardiol, Nishinomiya, Japan
[2] Gojinkai Sumiyoshigawa Hosp, Dept Nephrol, Kobe, Japan
关键词
2-oxoglutarate-dependent dioxygenases; alpha-ketoglutarate; epigenetics; HIF-PHIs; renal anemia; CHRONIC KIDNEY-DISEASE; FACTOR PATHWAY INHIBITOR; ALPHA-KETOGLUTARATE; ROXADUSTAT FG-4592; TISSUE FACTOR; MYOCARDIAL-INFARCTION; ENERGY-METABOLISM; RESPONSE ELEMENT; HEART; DYSFUNCTION;
D O I
10.1093/ckj/sfae051
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Hypoxia-inducible factor prolyl hydroxylase inhibitors (HIF-PHIs) have emerged as a novel therapeutic class for treating anemia in patients with chronic kidney disease. Small molecule analogs of alpha-ketoglutarate (AKG), an essential substrate for 2-oxoglutarate-dependent dioxygenases (2-OGDDs), including prolyl hydroxylase domain proteins (PHDs), inhibit PHDs pharmacologically and thereby prevent HIF degradation. HIF stabilization alleviates anemia through several stimulatory effects on erythropoiesis, but it also affects the expression of many anemia-unrelated genes whose protein products exert important functions in vivo. Therefore, the pleiotropic effects of HIF stabilization under normoxic conditions deserve to be examined in more detail. Specifically, we believe that particular attention should be given to epigenetic modifications among the various AKG-based metabolic systems that may be altered by HIF-PHIs. It is noteworthy that AKG has been reported to exert health-protective actions. AKG-based metabolic systems include enzymes associated with the tricarboxylic acid cycle and amino acid metabolism, as well as 2-OGDD-mediated processes, which play important roles in many biological reactions. In this review, we examine the multifaceted effects of HIF-PHIs, encompassing not only their on-target effect of HIF stabilization but also their off-target inhibitory effects on various AKG-based metabolic systems. Furthermore, we examine its potential relevance to cardiovascular complications, based on clinical and animal studies suggesting its involvement in vascular calcification, thrombogenesis and heart failure. In conclusion, although HIF-PHIs offer a promising avenue for anemia treatment in CKD patients, their broader impact on multiple biological systems raises substantial concerns. The intricate interplay between HIF stabilization, AKG competition and cardiovascular complications warrants extensive, long-term investigations to ensure the safety and usefulness of HIF-PHIs in clinical practice.
引用
收藏
页数:11
相关论文
共 50 条
  • [21] Discovery of DS-1093a: An oral hypoxia-inducible factor prolyl hydroxylase inhibitor for the treatment of renal anemia
    Tanaka, Naoki
    Fukuda, Takeshi
    Takano, Rieko
    Sasaki, Koji
    Tsuji, Takashi
    Goto, Riki
    Kuribayashi, Takeshi
    Yamaguchi, Kyoji
    Niitsu, Yoichi
    Ishii, Ken
    Hashimoto, Masami
    Takahashi, Shinichi
    Obayashi, Hisakuni
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2024, 111
  • [22] Hypoxia-inducible factor prolyl hydroxylase enzyme inhibitors: ready for primetime?
    Macdougall, Iain C.
    CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2022, 31 (05): : 399 - 405
  • [23] Hypoxia-inducible factor prolyl hydroxylase inhibitors in kidney transplant recipients
    Ogata, Masatomo
    Miyauchi, Takamasa
    Sakurai, Yuko
    Murata, Marie
    Shinoda, Kazunobu
    Shibagaki, Yugo
    Yazawa, Masahiko
    CLINICAL KIDNEY JOURNAL, 2022, 15 (05) : 1024 - 1026
  • [24] Hypoxia-Inducible Factor-Proline Hydroxylase Inhibitor in the Treatment of Renal Anemia
    Hu, Xiaofan
    Xie, Jingyuan
    Chen, Nan
    KIDNEY DISEASES, 2021, 7 (01) : 1 - 9
  • [25] Hypoxia-Inducible Factor-Prolyl Hydroxylase Domain Inhibitors to Treat Anemia in Chronic Kidney Disease
    Sakashita, Midori
    Tanaka, Tetsuhiro
    Nangaku, Masaomi
    CKD-ASSOCIATED COMPLICATIONS: PROGRESS IN THE LAST HALF CENTURY, 2019, 198 : 112 - 123
  • [26] Future perspectives of anemia management in chronic kidney disease using hypoxia-inducible factor-prolyl hydroxylase inhibitors
    Sugahara, Mai
    Tanaka, Tetsuhiro
    Nangaku, Masaomi
    PHARMACOLOGY & THERAPEUTICS, 2022, 239
  • [27] Photoactivatable Prolyl Hydroxylase 2 Inhibitors for Stabilizing the Hypoxia-Inducible Factor with Light
    Li, Zhihong
    Su, Kaijun
    Jiang, Zhensheng
    Yu, Yancheng
    You, Qidong
    Zhang, Xiaojin
    JOURNAL OF MEDICINAL CHEMISTRY, 2019, 62 (16) : 7583 - 7588
  • [28] Investigational hypoxia-inducible factor prolyl hydroxylase inhibitors (HIF-PHI) for the treatment of anemia associated with chronic kidney disease
    Del Vecchio, Lucia
    Locatelli, Francesco
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2018, 27 (07) : 613 - 621
  • [29] Iron Supplements Concomitant within Hypoxia-Inducible Factor Prolyl Hydroxylase Domain Inhibitors in the Treatment of Chronic Kidney Disease Anemia
    Wang, Xue
    Wei, Cuiting
    Zhao, Delong
    Sun, Xuefeng
    Zhu, Fengge
    Mei, Yan
    Ma, Qian
    Cai, Guangyan
    Chen, Xiangmei
    Li, Ping
    KIDNEY DISEASES, 2023, 9 (06) : 485 - 497
  • [30] Erythrocyte indices and response to hypoxia-inducible factor prolyl hydroxylase inhibitors in chronic kidney disease patients with renal anemia: a retrospective study
    Odajima, Kohei
    Arai, Shigeyuki
    Kido, Ryo
    Anzai, Hitoshi
    Gojo, Maika
    Taira, Shuntaro
    Matsui, Rena
    Fujigaki, Yoshihide
    Shibata, Shigeru
    BMC NEPHROLOGY, 2024, 25 (01)