Developing PI3K Inhibitors for Respiratory Diseases.

E Fagone, M Fruciano, E Gili, G Sambataro, Carlo Vancheri
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Abstract

A number of different experimental models using both non-selective and selective PI3K inhibitors have shown that many pathogenic steps of respiratory disorders, such as bronchial asthma, Chronic Obstructive Pulmonary Disease (COPD), Idiopathic Pulmonary Fibrosis (IPF), Acute Respiratory Distress Syndrome (ARDS) and Lung Cancer (LC) are, at least in part, regulated by the PI3K signaling pathway, suggesting that the inhibition of PI3K could represent an ideal therapeutic target for the treatment of respiratory diseases. This chapter summarizes the current state of the therapeutic strategies aimed to exploit the inhibition of PI3K in this context. In animal models of asthma, selective δ and γ inhibitors have shown to be effective, and when administered by inhalation, reasonably safe. Nevertheless, very few clinical trials have been performed so far. The efficacy of current traditional therapies for allergic bronchial asthma has likely diminished the need for new alternative treatments. Surprisingly, in COPD, where instead there is an urgent need for new and more effective therapeutic approaches, the number of clinical studies is still low and not capable yet, with the exception for an acceptable safety profile, to show a significant improvement of clinical outcomes. In IPF, a disease with a disappointing prognosis, PI3K inhibitors have been bound to a FAP ligand with the aim to selectively target myofibroblasts, showing to significantly reduce collagen production and the development of lung fibrosis in an animal model of lung fibrosis. Due to its role in cell activation and cell replication, the PI3K pathway is obviously largely involved in lung cancer. Several studies, currently ongoing, are testing the effect of PI3K inhibitors mainly in NSCLC. Some evidence in the treatment of cancer patients suggests the possibility that PI3K inhibitors may enhance the response to conventional treatment. The involvement of PI3Kδ in the modulation of airway neutrophil recruitment and bronchial epithelial functional alterations also suggest a potential role in the treatment of ARDS, but at the current state the ongoing trials are aimed to the treatment of ARDS in COVID-19 patients. In general, few clinical trials investigating PI3K inhibitors in respiratory disorders have been performed so far. This relatively new approach of treatment is just at its beginning and certainly needs further efforts and additional studies.

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开发用于呼吸道疾病的PI3K抑制剂。
许多使用非选择性和选择性PI3K抑制剂的不同实验模型表明,呼吸系统疾病的许多致病步骤,如支气管哮喘、慢性阻塞性肺疾病(COPD)、特发性肺纤维化(IPF)、急性呼吸窘迫综合征(ARDS)和肺癌(LC),至少部分由PI3K信号通路调节。提示抑制PI3K可能是治疗呼吸系统疾病的理想靶点。本章总结了在这种情况下利用PI3K抑制的治疗策略的现状。在哮喘动物模型中,选择性δ和γ抑制剂已被证明是有效的,并且当通过吸入给药时,相当安全。然而,迄今为止进行的临床试验很少。目前传统疗法对过敏性支气管哮喘的疗效可能减少了对新的替代疗法的需求。令人惊讶的是,在COPD中,迫切需要新的更有效的治疗方法,但临床研究的数量仍然很少,除了可接受的安全性外,尚未能够显示临床结果的显着改善。在IPF这种预后令人失望的疾病中,PI3K抑制剂被结合到FAP配体上,目的是选择性地靶向肌成纤维细胞,在肺纤维化动物模型中显示出显著减少胶原生成和肺纤维化的发展。由于其在细胞活化和细胞复制中的作用,PI3K通路显然在很大程度上参与了肺癌。目前正在进行的几项研究正在测试PI3K抑制剂主要在NSCLC中的作用。一些治疗癌症患者的证据表明,PI3K抑制剂可能会增强对常规治疗的反应。PI3Kδ参与气道中性粒细胞募集和支气管上皮功能改变的调节也提示其在ARDS治疗中的潜在作用,但目前正在进行的试验旨在治疗COVID-19患者的ARDS。总的来说,到目前为止,研究PI3K抑制剂在呼吸系统疾病中的临床试验还很少。这种相对较新的治疗方法才刚刚开始,当然需要进一步的努力和额外的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.60
自引率
0.00%
发文量
26
审稿时长
>12 weeks
期刊介绍: The review series Current Topics in Microbiology and Immunology provides a synthesis of the latest research findings in the areas of molecular immunology, bacteriology and virology. Each timely volume contains a wealth of information on the featured subject. This review series is designed to provide access to up-to-date, often previously unpublished information.
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