Department of Otolaryngology, Head and Neck Surgery, Universität Bielefeld, Teutoburger Str. 50, 33604, Bielefeld, Germany.
Department of Medicine, National University of Singapore, and National University Health System, Singapore, Singapore.
Cell Commun Signal. 2022 Sep 19;20(1):148. doi: 10.1186/s12964-022-00953-w.
Middle ear cholesteatoma (MEC), is a destructive, and locally invasive lesion in the middle ear driven by inflammation with an annual incidence of 10 per 100,000. Surgical extraction/excision remains the only treatment strategy available and recurrence is high (up to 40%), therefore developing the first pharmaceutical treatments for MEC is desperately required. This review was targeted at connecting the dysregulated inflammatory network of MEC to pathogenesis and identification of pharmaceutical targets. We summarized the numerous basic research endeavors undertaken over the last 30+ years to identify the key targets in the dysregulated inflammatory pathways and judged the level of evidence for a given target if it was generated by in vitro, in vivo or clinical experiments. MEC pathogenesis was found to be connected to cytokines characteristic for Th1, Th17 and M1 cells. In addition, we found that the inflammation created damage associated molecular patterns (DAMPs), which further promoted inflammation. Similar positive feedback loops have already been described for other Th1/Th17 driven inflammatory diseases (arthritis, Crohn's disease or multiple sclerosis). A wide-ranging search for molecular targeted therapies (MTT) led to the discovery of over a hundred clinically approved drugs already applied in precision medicine. Based on exclusion criteria designed to enable fast translation as well as efficacy, we condensed the numerous MTTs down to 13 top drugs. The review should serve as groundwork for the primary goal, which is to provide potential pharmaceutical therapies to MEC patients for the first time in history. Video Abstract.
中耳胆脂瘤(MEC)是一种破坏性的、局部侵袭性病变,由炎症驱动,年发病率为每 10 万人中有 10 例。手术切除仍然是唯一可用的治疗策略,但复发率很高(高达 40%),因此迫切需要开发治疗 MEC 的第一种药物治疗方法。本综述旨在将 MEC 失调的炎症网络与发病机制和药物靶点的识别联系起来。我们总结了过去 30 多年来为确定失调炎症途径中的关键靶点而进行的许多基础研究工作,并根据体外、体内或临床实验产生的给定靶点的证据水平进行了判断。MEC 的发病机制与 Th1、Th17 和 M1 细胞特征性的细胞因子有关。此外,我们发现炎症产生了损伤相关分子模式(DAMPs),进一步促进了炎症。其他 Th1/Th17 驱动的炎症性疾病(关节炎、克罗恩病或多发性硬化症)也已经描述了类似的正反馈循环。对靶向治疗(MTT)的广泛搜索导致发现了 100 多种已在精准医学中应用的临床批准药物。根据旨在实现快速转化和疗效的排除标准,我们将众多 MTT 浓缩为 13 种顶级药物。该综述应作为首要目标的基础,这是首次为 MEC 患者提供潜在的药物治疗方法。