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泛赖氨酸氧化酶抑制剂 PXS-5505 通过抑制系统性硬化症啮齿动物模型中的胶原交联改善多器官纤维化。

Pan-Lysyl Oxidase Inhibitor PXS-5505 Ameliorates Multiple-Organ Fibrosis by Inhibiting Collagen Crosslinks in Rodent Models of Systemic Sclerosis.

机构信息

Drug Discovery, Pharmaxis Ltd., Sydney, NSW 2086, Australia.

Children's Cancer Institute, Lowy Cancer Research Centre, UNSW Sydney, Kensington, Sydney, NSW 2031, Australia.

出版信息

Int J Mol Sci. 2022 May 16;23(10):5533. doi: 10.3390/ijms23105533.

Abstract

Systemic sclerosis (SSc) is characterised by progressive multiple organ fibrosis leading to morbidity and mortality. Lysyl oxidases play a vital role in the cross-linking of collagens and subsequent build-up of fibrosis in the extracellular matrix. As such, their inhibition provides a novel treatment paradigm for SSc. A novel small molecule pan-lysyl oxidase inhibitor, PXS-5505, currently in clinical development for myelofibrosis treatment was evaluated using in vivo rodent models resembling the fibrotic conditions in SSc. Both lysyl oxidase and lysyl oxidase-like 2 (LOXL2) expression were elevated in the skin and lung of SSc patients. The oral application of PXS-5505 inhibited lysyl oxidase activity in the skin and LOXL2 activity in the lung. PXS-5505 exhibited anti-fibrotic effects in the SSc skin mouse model, reducing dermal thickness and α-smooth muscle actin. Similarly, in the bleomycin-induced mouse lung model, PXS-5505 reduced pulmonary fibrosis toward normal levels, mediated by its ability to normalise collagen/elastin crosslink formation. PXS-5505 also reduced fibrotic extent in models of the ischaemia-reperfusion heart, the unilateral ureteral obstruction kidney, and the CCl4-induced fibrotic liver. PXS-5505 consistently demonstrates potent anti-fibrotic efficacy in multiple models of organ fibrosis relevant to the pathogenesis of SSc, suggesting that it may be efficacious as a novel approach for treating SSc.

摘要

系统性硬化症(SSc)的特征是进行性多器官纤维化,导致发病率和死亡率增加。赖氨酰氧化酶在胶原蛋白的交联和细胞外基质中随后的纤维化形成中起着至关重要的作用。因此,它们的抑制为 SSc 提供了一种新的治疗范例。一种新型小分子泛赖氨酰氧化酶抑制剂 PXS-5505 目前正在开发用于治疗骨髓纤维化,在类似于 SSc 纤维化条件的体内啮齿动物模型中进行了评估。SSc 患者的皮肤和肺中均升高了赖氨酰氧化酶和赖氨酰氧化酶样 2(LOXL2)的表达。PXS-5505 的口服应用抑制了皮肤中的赖氨酰氧化酶活性和肺中的 LOXL2 活性。PXS-5505 在 SSc 皮肤小鼠模型中表现出抗纤维化作用,减少真皮厚度和α-平滑肌肌动蛋白。同样,在博来霉素诱导的小鼠肺模型中,PXS-5505 通过使其能够正常化胶原蛋白/弹性蛋白交联形成,将肺纤维化降低至正常水平。PXS-5505 还减少了缺血再灌注心脏、单侧输尿管梗阻肾脏和 CCl4 诱导的纤维化肝脏模型中的纤维化程度。PXS-5505 在与 SSc 发病机制相关的多种器官纤维化模型中始终表现出强大的抗纤维化功效,这表明它可能作为治疗 SSc 的新方法有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/216f/9146019/67399c813016/ijms-23-05533-g001.jpg

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