Taisir Bozo, Annette Murr, Birte Holtfreter, Sebastian-Edgar Baumeister, Peter Meisel, Uwe Völker, Werner Weitschies, Henry Völzke, Philipp Kanzow, Elke Hammer, Manuela Gesell Salazar, Thomas Kocher
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引用次数: 0
Abstract
Introduction: This explanatory pilot study presents a workflow to identify approved drugs, which could be repurposed for periodontitis therapy using salivary proteomics combined with drug-target database screening.
Methods: Proteomic analyses of saliva using LC-MS/MS were conducted in two independent settings: a cohort (sub-study I, N = 187) and case-control (sub-study II, N = 72). Statistical analyses were performed using both stringent and lenient criteria. Under the stringent (lenient) criteria, proteins were considered potential targets if they showed a q-value < 0.05 (< 0.1) in the cohort study and a p-value < 0.05 together with an absolute fold change > 1.5 (1.3) in the case-control study. Four databases were searched to assess whether these proteins are known targets of approved drugs.
Results: In the stringent (lenient) analysis one (26) proteins were associated with periodontitis in both studies, of which one (nine) were reported drug targets and one (seven) of those were potential drug targets in periodontitis. Target screening in databases identified 3/11 approved drugs, with eight of them having potential for repurposing for periodontal treatment. Several of these drugs (e.g., HDAC inhibitors, sivelestat, compstatin derivatives, auranofin, artenimol and bortezomib) have already shown efficacy in preclinical models of periodontal host modulation.
Conclusion: This exploratory pilot study provided insights into potential therapeutic targets and potential drugs for periodontitis treatment. This workflow may help to identify approved drugs that could be repurposed for periodontal treatment.
本解释性试点研究提出了一种鉴定批准药物的工作流程,这些药物可以利用唾液蛋白质组学结合药物靶标数据库筛选重新用于牙周炎治疗。方法:采用LC-MS/MS在两个独立的环境下进行唾液蛋白质组学分析:队列(子研究I, N = 187)和病例对照(子研究II, N = 72)。采用严格和宽松的标准进行统计分析。在严格(宽松)的标准下,在病例对照研究中,如果蛋白质的q值为1.5(1.3),则被认为是潜在的靶标。研究人员检索了四个数据库,以评估这些蛋白质是否是已批准药物的已知靶点。结果:在严格(宽松)分析中,两项研究中有1(26)种蛋白质与牙周炎相关,其中1(9)种是已报道的药物靶点,其中1(7)种是牙周炎的潜在药物靶点。数据库中的目标筛选确定了3/11已批准的药物,其中8种具有重新用于牙周治疗的潜力。其中一些药物(如HDAC抑制剂、西维司他、compstatin衍生物、金嘌呤、阿替尼摩和硼替佐米)已经在牙周宿主调节的临床前模型中显示出疗效。结论:本探索性初步研究为牙周炎治疗提供了潜在的治疗靶点和潜在的药物。该工作流程可能有助于确定可重新用于牙周治疗的批准药物。
期刊介绍:
Journal of Clinical Periodontology was founded by the British, Dutch, French, German, Scandinavian, and Swiss Societies of Periodontology.
The aim of the Journal of Clinical Periodontology is to provide the platform for exchange of scientific and clinical progress in the field of Periodontology and allied disciplines, and to do so at the highest possible level. The Journal also aims to facilitate the application of new scientific knowledge to the daily practice of the concerned disciplines and addresses both practicing clinicians and academics. The Journal is the official publication of the European Federation of Periodontology but wishes to retain its international scope.
The Journal publishes original contributions of high scientific merit in the fields of periodontology and implant dentistry. Its scope encompasses the physiology and pathology of the periodontium, the tissue integration of dental implants, the biology and the modulation of periodontal and alveolar bone healing and regeneration, diagnosis, epidemiology, prevention and therapy of periodontal disease, the clinical aspects of tooth replacement with dental implants, and the comprehensive rehabilitation of the periodontal patient. Review articles by experts on new developments in basic and applied periodontal science and associated dental disciplines, advances in periodontal or implant techniques and procedures, and case reports which illustrate important new information are also welcome.