High Expression of High-Mobility Group Box 1 in Menstrual Blood: Implications for Endometriosis

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This study found higher HMGB1 levels in menstrual blood compared to serum or peritoneal fluid, and HMGB1 treatment induced VEGF production in endometriotic stromal cells.

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This study measured high-mobility group box 1 (HMGB1) concentrations in menstrual blood and compared them with serum and peritoneal fluid in 139 patients, including 84 with endometriosis and 55 nonendometriotic gynecologic controls. It assessed receptor for advanced glycation end products (RAGE) expression in eutopic and ectopic endometrium by immunohistochemistry and examined RAGE and VEGF mRNA responses in human endometriotic stromal cells treated with HMGB1 and/or lipopolysaccharide (LPS). HMGB1 was higher in menstrual blood than in serum or peritoneal fluid, and HMGB1 (alone or with LPS) increased VEGF production in stromal cells; RAGE was present in both normal and ectopic endometrial tissue. The paper’s key limitation is that its mechanistic experiments rely on in vitro stimulation rather than direct demonstration that HMGB1 complexes with other menstrual factors cause endometriosis in vivo. This paper is centrally about endometriosis — it links elevated HMGB1 in menstrual blood, through HMGB1/RAGE signaling, to inflammatory and angiogenic effects relevant to ectopic endometrial growth.

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Abstract

Endometriosis is a benign gynecologic disease characterized by the presence of ectopic endometrium and associated with inflammation and immune abnormalities. However, the molecular basis for endometriosis is not well understood. To address this issue, the present study examined the expression of high-mobility group box (HMGB) 1 in menstrual blood to investigate its role in the ectopic growth of human endometriotic stromal cells (ESCs). A total of 139 patients were enrolled in this study; 84 had endometriosis and 55 were nonendometriotic gynecological patients (control). The HMGB1 levels in various fluids were measured by enzyme-linked immunosorbent assay. Expression of receptor for advanced glycation end products (RAGE) in eutopic and ectopic endometrium was assessed by immunohistochemistry, and RAGE and vascular endothelial growth factor ( VEGF) messenger RNA expression in HMGB1- and lipopolysaccharide (LPS)-treated ESCs was evaluated by real-time polymerase chain reaction. The HMGB1 concentration was higher in menstrual blood than in serum or peritoneal fluid ( P < .001 for both). RAGE was expressed in both normal and ectopic endometrium. Administration of 1000 ng/mL HMGB1 or coadministration of 100 ng/mL HMGB1 and 100 ng/mL LPS induced VEGF production in ESCs relative to the control ( P < .05). These results suggest that menstrual fluid has naturally high levels of HMGB1 and may promote endometriosis following retrograde menstruation when complexed with other factors such as LPS by inducing inflammation and angiogenesis.
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Abstract

Endometriosis is a benign gynecologic disease characterized by the presence of ectopic endometrium and associated with inflammation and immune abnormalities. However, the molecular basis for endometriosis is not well understood. To address this issue, the present study examined the expression of high-mobility group box (HMGB) 1 in menstrual blood to investigate its role in the ectopic growth of human endometriotic stromal cells (ESCs). A total of 139 patients were enrolled in this study; 84 had endometriosis and 55 were nonendometriotic gynecological patients (control). The HMGB1 levels in various fluids were measured by enzyme-linked immunosorbent assay. Expression of receptor for advanced glycation end products (RAGE) in eutopic and ectopic endometrium was assessed by immunohistochemistry, and RAGE and vascular endothelial growth factor (VEGF) messenger RNA expression in HMGB1- and lipopolysaccharide (LPS)-treated ESCs was evaluated by real-time polymerase chain reaction. The HMGB1 concentration was higher in menstrual blood than in serum or peritoneal fluid (P <.001 for both). RAGE was expressed in both normal and ectopic endometrium. Administration of 1000 ng/mL HMGB1 or coadministration of 100 ng/mL HMGB1 and 100 ng/mL LPS induced VEGF production in ESCs relative to the control (P <.05). These results suggest that menstrual fluid has naturally high levels of HMGB1 and may promote endometriosis following retrograde menstruation when complexed with other factors such as LPS by inducing inflammation and angiogenesis. Similar content being viewed by others

References

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endometriosis

MeSH descriptors

Endometriosis HMGB1 Protein Menstruation Adult Biomarkers Biomarkers Endometriosis Endometriosis Endometriosis Endometrium Endometrium Endometrium Female Gene Expression HMGB1 Protein HMGB1 Protein HMGB1 Protein Humans Menstruation Middle Aged

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