帕罗瓦罗汀(Sohonos),一种用于减少渐进性纤维性骨化症异位骨化的合成维甲酸:历史、现在和未来。

IF 3.4 Q2 ENDOCRINOLOGY & METABOLISM JBMR Plus Pub Date : 2024-11-19 eCollection Date: 2025-01-01 DOI:10.1093/jbmrpl/ziae147
Edward C Hsiao, Maurizio Pacifici
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引用次数: 0

摘要

类维生素A是维生素A的代谢衍生物,在产前和产后发育过程中对各种组织和器官的调节起着至关重要的作用。活性类维甲酸,如全反式维甲酸,在细胞质中合成,随后与核维甲酸受体(RARα, RARβ和RARγ)相互作用,以增强特定基因的转录。在缺乏类维生素a的情况下,RARs仍然可以结合靶基因的应答元件,但抑制其转录。生长板中软骨细胞分化和软骨成熟需要缺乏类视黄醇信号和未配体RARs的转录抑制。这导致了一种假设,即合成类维甲酸激动剂可能是抑制这些细胞过程的药物,并在异位骨化(HO)等情况下对抗软骨和骨的过度形成。HO可以由多种原因引起,包括创伤、侵入性手术、炎症性疾病或遗传条件。一种这样的遗传性疾病是进行性骨化纤维发育不良(FOP),这是一种由激活ACVR1基因突变驱动的罕见疾病。FOP患者在软组织中有严重和进行性的HO形成,导致广泛的永久性活动能力丧失和死亡率增加。在小鼠模型中,选择性RARα或RARγ的合成类视黄醇激动剂对损伤性和遗传性HO具有抑制作用。RARγ激动剂显示出最高的有效性,palovarotene被选择用于FOP患者的临床试验。II期和III期临床试验的事后分析显示,帕伐罗汀对FOP有显著的疾病改善作用,但在一些年轻受试者中存在显著的风险,如生长板过早闭合。本文综述了类维甲酸和RAR在骨骼发育中的作用,并讨论了帕洛维烯作为一种潜在的FOP治疗药物的鉴定,支持其在一些国家监管部门批准的临床数据,以及该药物在除FOP外的其他相关疾病的潜在应用。
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Palovarotene (Sohonos), a synthetic retinoid for reducing new heterotopic ossification in fibrodysplasia ossificans progressiva: history, present, and future.

Retinoids are metabolic derivatives of vitamin A and play crucial roles in the regulation of various tissues and organs during prenatal and postnatal development. Active retinoids, like all-trans-retinoic acid, are synthesized in the cytoplasm and subsequently interact with nuclear retinoic acid receptors (RARα, RARβ, and RARγ) to enhance transcription of specific genes. In the absence of retinoids, RARs can still bind to response elements of target genes but repress their transcription. Chondrogenic cell differentiation and cartilage maturation in the growth plate require the absence of retinoid signaling and transcriptional repression by unliganded RARs. This led to the hypothesis that synthetic retinoid agonists may be pharmacological agents to inhibit those cellular processes and counter the excessive formation of cartilage and bone in conditions like heterotopic ossification (HO). HO can be instigated by diverse culprits including trauma, invasive surgeries, inflammatory disorders, or genetic conditions. One such genetic disease is fibrodysplasia ossificans progressiva (FOP), a rare disorder driven by activating mutations in the ACVR1 gene. Patients with FOP have severe and progressive HO formation in soft tissues, leading to extensive permanent loss of mobility and increased mortality. Synthetic retinoid agonists selective for RARα or RARγ showed efficacy against injury-induced and genetic HO in mouse models. The RARγ agonists showed the highest effectiveness, with palovarotene being selected for clinical trials in patients with FOP. Post hoc analyses of phase II and phase III clinical trials showed that palovarotene has significant disease-modifying effects for FOP, but with significant risks such as premature growth plate closure in some younger subjects. This review provides an overview of retinoid and RAR roles in skeletal development and discusses the identification of palovarotene as a potential FOP therapy, the clinical data supporting its regulatory approval in some countries, and the potential applications of this drug for other relevant disorders besides FOP.

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来源期刊
JBMR Plus
JBMR Plus Medicine-Orthopedics and Sports Medicine
CiteScore
5.80
自引率
2.60%
发文量
103
审稿时长
8 weeks
期刊最新文献
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