Meng-Yao Wang, Ru-Ru Pan, Jie Zhou, Xiao Wen, Sha-Sha Chen, Chang Yuan, Yan-Lu Han, Lu Tang, Hao Wang, Wen-Quan Hu, Han Xiao, Ya-Jun Duan, Ze-Qun Yin, Shuang Zhang
{"title":"光甘草定恢复细胞周期蛋白A2可逆转病理性细胞周期阻滞并促进HFpEF的心脏修复。","authors":"Meng-Yao Wang, Ru-Ru Pan, Jie Zhou, Xiao Wen, Sha-Sha Chen, Chang Yuan, Yan-Lu Han, Lu Tang, Hao Wang, Wen-Quan Hu, Han Xiao, Ya-Jun Duan, Ze-Qun Yin, Shuang Zhang","doi":"10.1038/s41401-026-01952-0","DOIUrl":null,"url":null,"abstract":"<p><p>Heart failure with preserved ejection fraction (HFpEF) is a pervasive clinical syndrome characterized by complex and elusive pathogenic mechanisms. In this study, we identify aberrant cardiomyocyte cell cycle arrest as a previously unrecognized pathological driver of HFpEF that hinders tissue repair. Using in vivo and in vitro models, we further demonstrate that Glabridin (Gla), a bioactive isoflavone, can induce cardiac repair and alleviate myocardial hypertrophy and fibrosis in HFpEF by targeting the cell cycle arrest pathway. Mechanistically, Gla exerts its protective effects by specifically inhibiting the degradation of Cyclin A2 (CCNA2) and mitigating cardiomyocyte oxidative damage. This stabilization of CCNA2 effectively abrogates cell cycle arrest and drives cardiomyocyte cell cycle re-entry, an effect that was successfully recapitulated by CCNA2 gain-of-function experiments. This reparative response is intrinsically coupled with the restoration of metabolic homeostasis and the attenuation of oxidative stress, as evidenced in both cardiac and hepatic cells. Collectively, our findings define cell cycle arrest as a novel target and position Gla as a potent inducer of CCNA2-mediated cardiac repair for HFpEF treatment.</p>","PeriodicalId":6942,"journal":{"name":"Acta Pharmacologica Sinica","volume":" ","pages":""},"PeriodicalIF":10.4000,"publicationDate":"2026-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Restoration of cyclin A2 by glabridin reverses pathological cell cycle arrest and drives cardiac repair in HFpEF.\",\"authors\":\"Meng-Yao Wang, Ru-Ru Pan, Jie Zhou, Xiao Wen, Sha-Sha Chen, Chang Yuan, Yan-Lu Han, Lu Tang, Hao Wang, Wen-Quan Hu, Han Xiao, Ya-Jun Duan, Ze-Qun Yin, Shuang Zhang\",\"doi\":\"10.1038/s41401-026-01952-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Heart failure with preserved ejection fraction (HFpEF) is a pervasive clinical syndrome characterized by complex and elusive pathogenic mechanisms. In this study, we identify aberrant cardiomyocyte cell cycle arrest as a previously unrecognized pathological driver of HFpEF that hinders tissue repair. Using in vivo and in vitro models, we further demonstrate that Glabridin (Gla), a bioactive isoflavone, can induce cardiac repair and alleviate myocardial hypertrophy and fibrosis in HFpEF by targeting the cell cycle arrest pathway. Mechanistically, Gla exerts its protective effects by specifically inhibiting the degradation of Cyclin A2 (CCNA2) and mitigating cardiomyocyte oxidative damage. This stabilization of CCNA2 effectively abrogates cell cycle arrest and drives cardiomyocyte cell cycle re-entry, an effect that was successfully recapitulated by CCNA2 gain-of-function experiments. This reparative response is intrinsically coupled with the restoration of metabolic homeostasis and the attenuation of oxidative stress, as evidenced in both cardiac and hepatic cells. Collectively, our findings define cell cycle arrest as a novel target and position Gla as a potent inducer of CCNA2-mediated cardiac repair for HFpEF treatment.</p>\",\"PeriodicalId\":6942,\"journal\":{\"name\":\"Acta Pharmacologica Sinica\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":10.4000,\"publicationDate\":\"2026-10-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Pharmacologica Sinica\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1038/s41401-026-01952-0\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Pharmacologica Sinica","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41401-026-01952-0","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Restoration of cyclin A2 by glabridin reverses pathological cell cycle arrest and drives cardiac repair in HFpEF.
Heart failure with preserved ejection fraction (HFpEF) is a pervasive clinical syndrome characterized by complex and elusive pathogenic mechanisms. In this study, we identify aberrant cardiomyocyte cell cycle arrest as a previously unrecognized pathological driver of HFpEF that hinders tissue repair. Using in vivo and in vitro models, we further demonstrate that Glabridin (Gla), a bioactive isoflavone, can induce cardiac repair and alleviate myocardial hypertrophy and fibrosis in HFpEF by targeting the cell cycle arrest pathway. Mechanistically, Gla exerts its protective effects by specifically inhibiting the degradation of Cyclin A2 (CCNA2) and mitigating cardiomyocyte oxidative damage. This stabilization of CCNA2 effectively abrogates cell cycle arrest and drives cardiomyocyte cell cycle re-entry, an effect that was successfully recapitulated by CCNA2 gain-of-function experiments. This reparative response is intrinsically coupled with the restoration of metabolic homeostasis and the attenuation of oxidative stress, as evidenced in both cardiac and hepatic cells. Collectively, our findings define cell cycle arrest as a novel target and position Gla as a potent inducer of CCNA2-mediated cardiac repair for HFpEF treatment.
期刊介绍:
APS (Acta Pharmacologica Sinica) welcomes submissions from diverse areas of pharmacology and the life sciences. While we encourage contributions across a broad spectrum, topics of particular interest include, but are not limited to: anticancer pharmacology, cardiovascular and pulmonary pharmacology, clinical pharmacology, drug discovery, gastrointestinal and hepatic pharmacology, genitourinary, renal, and endocrine pharmacology, immunopharmacology and inflammation, molecular and cellular pharmacology, neuropharmacology, pharmaceutics, and pharmacokinetics. Join us in sharing your research and insights in pharmacology and the life sciences.