Expression levels of circulatory mir-185-5p, vascular endothelial growth factor, and platelet-derived growth factor target genes in endometriosis

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Circulating miR-185-5p was significantly downregulated in women with endometriosis compared to controls, with potential diagnostic utility, while VEGF and PDGF target genes showed no significant expression differences.

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AI-generated deep summary by claude@2026-06, 2026-06-10 · read from full text

This cross-sectional study evaluated circulating miR-185-5p and predicted downstream angiogenesis-related target genes VEGF-A and PDGF in whole blood from 25 laparoscopically confirmed grade III–IV endometriosis patients versus 25 age-matched controls without endometriosis, using whole-genome miRNA sequencing followed by qRT-PCR validation. Small RNA sequencing identified 30 significantly differentially expressed mature miRNAs between groups, with miR-185-5p showing significantly lower expression in serum/plasma of endometriosis patients (p < 0.001), while whole-blood miR-185-5p did not significantly differ between groups; VEGF-A and PDGF target gene expression was measured after normalization to housekeeping controls. The authors highlight demographic differences between groups (BMI and CA-125) as potential confounders and used a limited sample size. This paper is centrally about endometriosis — it reports differential circulating miR-185-5p expression (and its relation to VEGF-A/PDGF angiogenic pathways) in women with endometriosis.

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Abstract

BACKGROUND: Using blood-based biomarkers such as microRNAs (miRNAs) may allow particularly effective and minimally invasive diagnosis and treatment of endometriosis. Objective: We evaluated the differential expression of circulating miRNA-185-5p (miR-185-5p), vascular endothelial growth factor (VEGF), and platelet-derived growth factor (PDGF) target genes between endometriosis and healthy women. MATERIALS AND METHODS: 25 women with a history of endometriosis (grad III-IV) diagnosed by laparoscopy as the case group and 25 women without endometriosis underwent laparoscopy for ovarian cysts or pelvic pain as the control group were enrolled in this case-control study. Blood samples were obtained, and total RNA was used for high-throughput small RNA sequencing, and this was confirmed by means of quantitative real-time polymerase chain reaction (qRT-PCR). RESULTS: miRNA expression profiling using non-coding RNA sequencing revealed that one miRNA including miR-185-5p was significantly down-regulated in the case group compared with the controls. The qRT-PCR results showed significant downregulation of the expression level of miR-185-5p (p < 0.01) in the plasma of the case group. Receiver operating characteristic (ROC) curve analysis showed the area of miR-185-5p under the ROC curve for endometriosis diagnosis was 0.919 (p < 0.001). The RT-PCR results demonstrated that there was no significant difference in the expression of VEGF and PDGF mRNA of blood samples in the cases compared to the control group (PDGF, p = 0.09 and VEGF, p = 0.36). CONCLUSION: The low expression of miR-185-5p in the plasma of women with endometriosis could be employed as an important non-invasive biomarker for early detection and screening of endometriosis by blood samples.
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Section

Our findings proposed miR-185-5p as a novel biomarker and regulator in endometriosis pathogenesis, and these findings support the notion that target therapies against miR-185-5p should have priority in targeting PDGF and VEGF . They are therefore promising tools in therapeutic developments to control the progression and metastasis processes in endometriosis patients. Overall, the results of the statistical analysis suggest miR-185-5p as a potential biomarker of disease activity in endometriosis.

Coi Statement

The authors declare that there are no conflicts of interest.

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endometriosis

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europepmc
last seen: 2026-06-17T06:13:18.893374+00:00
pubmed
last seen: 2026-05-13T22:21:53.586419+00:00
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last seen: 2026-05-14T19:30:52.867331+00:00
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