Zhu Junjie, Qin Fu-Ying, Lei Saifei, Gu Ruizhi, Qi Qian, Lu Jie, Anderson Karl E, Wipf Peter, Ma Xiaochao
Center for Pharmacogenetics, Department of Pharmaceutical Sciences, School of Pharmacy, University of Pittsburgh, Pittsburgh, PA, USA.
Porphyria Laboratory & Center, Department of Internal Medicine, University of Texas Medical Branch, Galveston, TX, USA.
Nat Commun. 2024 Dec 4;15(1):10557. doi: 10.1038/s41467-024-54969-6.
Erythropoietic protoporphyria (EPP) is a genetic disease characterized by protoporphyrin IX-mediated painful phototoxicity. Currently, options for the management of EPP-associated phototoxicity are limited and no oral medication is available. Here, we investigated a novel therapy against EPP-associated phototoxicity by targeting the ATP-binding cassette subfamily G member 2 (ABCG2), the efflux transporter of protoporphyrin IX. Oral ABCG2 inhibitors were developed, and they successfully prevented EPP-associated phototoxicity in a genetically engineered EPP mouse model. Mechanistically, ABCG2 inhibitors suppress protoporphyrin IX release from erythroid cells and reduce the systemic exposure to protoporphyrin IX in EPP. In summary, our work establishes a novel strategy for EPP therapy by targeting ABCG2 and provides oral ABCG2 inhibitors that can effectively prevent protoporphyrin IX-mediated phototoxicity in mice.
红细胞生成性原卟啉病(EPP)是一种遗传性疾病,其特征为原卟啉IX介导的疼痛性光毒性。目前,EPP相关光毒性的治疗选择有限,且尚无口服药物可用。在此,我们通过靶向原卟啉IX的外排转运体——ATP结合盒亚家族G成员2(ABCG2),研究了一种针对EPP相关光毒性的新疗法。开发了口服ABCG2抑制剂,它们在基因工程EPP小鼠模型中成功预防了EPP相关的光毒性。从机制上讲,ABCG2抑制剂可抑制原卟啉IX从红系细胞释放,并减少EPP中原卟啉IX的全身暴露。总之,我们的工作通过靶向ABCG2建立了一种EPP治疗的新策略,并提供了可有效预防小鼠中原卟啉IX介导的光毒性的口服ABCG2抑制剂。