Burns Katherine A, Peterse Daniëlle, Appleyard Caroline B, Chandler Ronald, Guo Sun-Wei, Pearson Amelia, Persoons Eleonora, Anglesio Michael S, Rogers Michael S, Sharpe-Timms Kathy L, Vriens Joris, McAllister Stacey L, Dodds Kelsi N, Cousins Fiona L, Hummelshoj Lone, Missmer Stacey A, Bruner-Tran Kaylon L, Greaves Erin
Department of Environmental and Public Health Sciences, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Department of Surgery, Vascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Mol Hum Reprod. 2025 Jul 3;31(3). doi: 10.1093/molehr/gaaf021.
In vivo models of endometriosis enable the discovery and preclinical testing of new therapies. Several rodent models of endometriosis exist, but a lack of harmonization impedes reproducibility and comparability of results among investigators. Homologous models are advantageous as they allow the contribution of the immune system/inflammation to be studied. We reviewed published homologous rodent models of endometriosis to develop standard operating procedures ('EPHect-EM-Homologous-SOPs') to guide and facilitate the choice and implementation of these models and harmonize documentation to enhance interpretation and comparability of results. The World Endometriosis Research Foundation (WERF) established an international working group of experts in models of endometriosis and formed a working sub-group to discuss homologous rodent models of endometriosis. A systematic literature review and detailed analysis of protocols was performed. The identified models have advantages and limitations regarding physiological relevance and utility. To harmonize key variables for endometriosis rodent models, the working group focused on species and animal strains, placement of ectopic tissue, uterine tissue volume, method of induction, hormonal status, and uterine tissue 'type'. A decision tree and recommendations on model use were developed for mice and rats to serve as guides for the use of harmonized EPHect-EM-Homologous-SOPs, experimental design, reporting standards, and research of question-dependent key variables. No 'ideal' homologous model of endometriosis was identified. The choice of model for specific research should be guided according to a best-fit strategy. Harmonization of SOPs, documentation, and reporting standards will improve replicability and translational applicability of studies and better highlight where de novo model creation is needed.
子宫内膜异位症的体内模型有助于新疗法的发现和临床前测试。目前存在多种啮齿动物子宫内膜异位症模型,但缺乏统一标准阻碍了研究人员之间结果的可重复性和可比性。同源模型具有优势,因为它们能够研究免疫系统/炎症的作用。我们回顾了已发表的同源啮齿动物子宫内膜异位症模型,以制定标准操作程序(“EPHect-EM-同源-SOPs”),指导并促进这些模型的选择和应用,统一记录方式以增强结果的解读和可比性。世界子宫内膜异位症研究基金会(WERF)成立了一个子宫内膜异位症模型国际专家工作组,并组建了一个工作小组来讨论同源啮齿动物子宫内膜异位症模型。我们进行了系统的文献综述和方案详细分析。已确定的模型在生理相关性和实用性方面各有优缺点。为统一子宫内膜异位症啮齿动物模型的关键变量,工作组重点关注物种和动物品系、异位组织的植入位置、子宫组织体积、诱导方法、激素状态以及子宫组织“类型”。针对小鼠和大鼠制定了模型使用决策树和建议,作为使用统一的EPHect-EM-同源-SOPs、实验设计、报告标准以及研究问题相关关键变量的指南。未发现“理想”的同源子宫内膜异位症模型。特定研究的模型选择应根据最佳匹配策略进行指导。SOPs、记录方式和报告标准的统一将提高研究的可重复性和转化适用性,并更好地突出需要创建新模型的领域。