Degano Matilde, Vesca Giorgia, Bulfoni Michela, Zermano Silvia, Restaino Stefano, Arcieri Martina, Zupi Errico, Seracchioli Renato, Driul Lorenza, Cesselli Daniela, Scambia Giovanni, Biasioli Anna, Vizzielli Giuseppe
Clinic of Obstetrics and Gynecology, Santa Maria della Misericordia University Hospital, Azienda Sanitaria Universitaria Friuli Centrale, 33100 Udine, Italy.
Institute of Pathology, Santa Maria della Misericordia University Hospital, Azienda Sanitaria Universitaria Friuli Centrale, 33100 Udine, Italy.
Biomolecules. 2025 Mar 27;15(4):493. doi: 10.3390/biom15040493.
This feasibility study explores the potential of salivary microRNAs (miRNAs) as non-invasive biomarkers for diagnosing endometriosis and assessing treatment response. Almost one-third of patients with endometriosis do not respond to the standard progestin treatment due to various mechanisms of progesterone resistance. MiRNAs, recognized for their stability in body fluids and role in gene regulation, may offer new diagnostic and prognostic opportunities as they are involved in the pathogenic pathways of endometriosis and progesterone resistance. We sequenced salivary miRNAs in three cohorts of patients: control women without endometriosis and patients with endometriosis who responded and did not respond to standard progestin treatment. This aims to identify the differential miRNA expression profiles associated with therapeutic response to dienogest. The preliminary results demonstrate the feasibility of miRNA sequencing from saliva and reveal distinct miRNA profiles between responders, non-responders, and controls. Key miRNAs, including mir-3168, the mir-200a family, and mir-93-5p, emerged as potential biomarkers, showing significant differential expression linked to both endometriosis presence and treatment response. Further validation of these findings in larger cohorts could pave the way for miRNA-based diagnostic and prognostic tools, potentially reducing diagnostic delays and personalizing treatment approaches for endometriosis patients, also with new target therapies.
这项可行性研究探讨了唾液微小RNA(miRNA)作为诊断子宫内膜异位症和评估治疗反应的非侵入性生物标志物的潜力。由于多种孕酮抵抗机制,近三分之一的子宫内膜异位症患者对标准孕激素治疗无反应。miRNA因其在体液中的稳定性及其在基因调控中的作用而被认可,由于其参与子宫内膜异位症和孕酮抵抗的致病途径,可能提供新的诊断和预后机会。我们对三组患者的唾液miRNA进行了测序:无子宫内膜异位症的对照女性以及对标准孕激素治疗有反应和无反应的子宫内膜异位症患者。这旨在确定与地诺孕素治疗反应相关的差异miRNA表达谱。初步结果证明了从唾液中进行miRNA测序的可行性,并揭示了反应者、无反应者和对照者之间不同的miRNA谱。关键的miRNA,包括mir-3168、mir-200a家族和mir-93-5p,成为潜在的生物标志物,显示出与子宫内膜异位症的存在和治疗反应均相关的显著差异表达。在更大的队列中对这些发现进行进一步验证,可能为基于miRNA的诊断和预后工具铺平道路,有可能减少诊断延迟并为子宫内膜异位症患者个性化治疗方法,也包括新的靶向治疗。