Single-Cell RNA Sequencing of PBMCs Identified Junction Plakoglobin (JUP) as Stratification Biomarker for Endometriosis.

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Single-cell RNA sequencing of PBMCs revealed junction plakoglobin (JUP) as a dysregulated gene in CD16+ monocytes, with elevated serum JUP levels correlating with endometriosis severity and enhancing CA125 diagnostic specificity.

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AI-generated deep summary by claude@2026-07, 2026-07-15 · read from full text

I can’t access the paper’s content because the page is blocked by an anti-bot/Proof-of-Work challenge, so I don’t have the methods or results needed to accurately summarize what was studied and what the authors found. Without the full text, any summary would require guessing, which would violate your requirement to base the summary on the paper’s actual content. The paper title claims it uses single-cell RNA sequencing of PBMCs to identify junction plakoglobin (JUP) as a stratification biomarker for endometriosis, but I can’t verify the study design or findings from the provided material. This paper is centrally about endometriosis — it is purported to identify JUP from single-cell PBMC data as an endometriosis stratification biomarker.

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Abstract

This study aimed to identify unique characteristics in the peripheral blood mononuclear cells (PBMCs) of endometriosis patients and develop a non-invasive early diagnostic tool. Using single-cell RNA sequencing (scRNA-seq), we constructed the first single-cell atlas of PBMCs from endometriosis patients based on 107,964 cells and 25,847 genes. Within CD16+ monocytes, we discovered JUP as a dysregulated gene. To assess its diagnostic potential, we measured peritoneal fluid (PF) and serum JUP levels in a large cohort of 199 patients including 20 women with ovarian cancer (OC). JUP was barely detectable in PF but was significantly elevated in the serum of patients with endometriosis and OC, with levels 1.33 and 2.34 times higher than controls, respectively. Additionally, JUP was found in conditioned culture media of CD14+/CD16+ monocytes aligning with our scRNA-seq data. Serum JUP levels correlated with endometriosis severity and endometrioma presence but were unaffected by dysmenorrhea, menstrual cycle, or adenomyosis. When combined with CA125 (cancer antigen 125) JUP enhanced the specificity of endometriosis diagnosis from 89.13% (CA125 measured alone) to 100%. While sensitivity remains a challenge at 19%, our results suggest that JUP's potential to enhance diagnostic accuracy warrants additional investigation. Furthermore, employing serum JUP as a stratification marker unlocked the potential to identify additional endometriosis-related genes, offering novel insights into disease pathogenesis.
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endometriosisadenomyosisendometriomadysmenorrhea

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last seen: 2026-05-10T10:54:59.177519+00:00
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