Margaria Jean Piero, Moretta Lucia, Alves-Filho Jose Carlos, Hirsch Emilio
Department of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Via Nizza 52, 10126 Torino, Italy.
Department of Pharmacology, Ribeirão Preto Medical School, University of São Paulo, Avenida Bandeirantes 3900, Ribeirao Preto 14049-900, Brazil.
Biomedicines. 2022 Mar 23;10(4):756. doi: 10.3390/biomedicines10040756.
Pulmonary fibrosis is a pathological fibrotic process affecting the lungs of five million people worldwide. The incidence rate will increase even more in the next years due to the long-COVID-19 syndrome, but a resolving treatment is not available yet and usually prognosis is poor. The emerging role of the phosphatidylinositol 3-kinase (PI3K)/AKT signaling in fibrotic processes has inspired the testing of drugs targeting the PI3K/Akt pathway that are currently under clinical evaluation. This review highlights the progress in understanding the role of PI3K/Akt in the development of lung fibrosis and its causative pathological context, including sepsis as well as acute lung injury (ALI) and its consequent acute respiratory distress syndrome (ARDS). We further summarize current knowledge about PI3K inhibitors for pulmonary fibrosis treatment, including drugs under development as well as in clinical trials. We finally discuss how the design of inhaled compounds targeting the PI3K pathways might potentiate efficacy and improve tolerability.
肺纤维化是一种影响全球500万人肺部的病理性纤维化过程。由于长期新冠综合征,未来几年发病率还会进一步上升,但目前尚无有效的治疗方法,且通常预后较差。磷脂酰肌醇3激酶(PI3K)/蛋白激酶B(AKT)信号传导在纤维化过程中日益凸显的作用,激发了对靶向PI3K/Akt途径药物的试验,这些药物目前正在进行临床评估。本综述重点介绍了在理解PI3K/Akt在肺纤维化发展中的作用及其致病病理背景方面取得的进展,包括脓毒症以及急性肺损伤(ALI)及其导致的急性呼吸窘迫综合征(ARDS)。我们进一步总结了目前关于用于治疗肺纤维化的PI3K抑制剂的知识,包括正在研发和临床试验中的药物。我们最后讨论了靶向PI3K途径的吸入性化合物的设计如何可能提高疗效并改善耐受性。