Floris Erica, Cozzolino Claudia, Marconi Sangar, Tonicello Fabiana, Picchio Vittorio, Pagano Francesca, Chimenti Isotta
Department of Medical Surgical Sciences and Biotechnologies, Sapienza University, 04100 Latina, Italy.
Institute of Biochemistry and Cell Biology, National Council of Research (IBBC-CNR), 00015 Monterotondo, Italy.
Rev Cardiovasc Med. 2023 Aug 8;24(8):226. doi: 10.31083/j.rcm2408226. eCollection 2023 Aug.
Cardiovascular diseases are the first cause of death worldwide, with a heavy social and economic impact. They include a wide range of pathological conditions, among which cardiac fibrosis represents a common pathogenetic hallmark. The fibrotic process is driven by cardiac mesenchymal stromal cells, namely fibroblasts, which become activated, proliferate, and differentiate into myofibroblasts in response to several stimuli, in the end secreting extracellular matrix proteins, and mediating cardiac tissue remodelling and stiffening. A specific therapy for the exclusive treatment of cardiac fibrosis is still lacking. Given the growing quest for reducing the burden of cardiovascular diseases, there is increasing interest in the search for new effective anti-fibrotic therapies. In this review, we will briefly summarize the limited pharmacological therapies known to act, at least in part, against cardiac fibrosis. Then we will present novel potential active molecules, molecular targets, and biotechnological approaches emerged in the last decade, as possible future therapeutic strategies for cardiac fibrosis, with a specific focus on targeting fibroblast activation and function.
心血管疾病是全球首要死因,具有重大的社会和经济影响。它们包括多种病理状况,其中心脏纤维化是一个常见的发病机制标志。纤维化过程由心脏间充质基质细胞(即成纤维细胞)驱动,这些细胞在受到多种刺激后被激活、增殖并分化为肌成纤维细胞,最终分泌细胞外基质蛋白,并介导心脏组织重塑和硬化。目前仍缺乏专门用于治疗心脏纤维化的特定疗法。鉴于减轻心血管疾病负担的需求不断增加,人们对寻找新的有效抗纤维化疗法的兴趣日益浓厚。在本综述中,我们将简要总结已知至少部分作用于心脏纤维化的有限药物疗法。然后,我们将介绍过去十年中出现的新型潜在活性分子、分子靶点和生物技术方法,作为心脏纤维化未来可能的治疗策略,特别关注靶向成纤维细胞的激活和功能。