Identification of urine biomarkers of endometriosis-Protein mass spectrometry

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This study analyzed urine proteomes to identify potential protein biomarkers of endometriosis using LC-MS/MS in 16 patients with endometriosis and 16 controls with functional ovarian cysts, with diagnoses confirmed by pathohistology. The authors found significantly different concentrations of 14 proteins between groups, including higher levels of proteins involved in immune activation (SELL), iron metabolism (HAMP), and cell apoptosis (CHGA) in endometriosis, and lower levels of antioxidant and extracellular matrix proteolysis-related proteins (SOD1 and MMP-9). The paper presents these proteomic differences as consistent with known disease-pathway dysregulation but is limited by the small cohort size and cross-sectional design. This paper is centrally about endometriosis — it identifies candidate urinary protein biomarkers of the disease using urine proteomics.

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Abstract

INTRODUCTION: Endometriosis is a chronic inflammatory disease that leads to a series of pathological reactions. The basis is a changed proinflammatory activated immune system, which results in more pronounced oxidative stress, disturbed function of proteolysis and cell apoptosis. These processes are crucial in the development of the disease because their dysfunctional activities cause the progression of the disease. It is believed that the proteins excreted in the urine interact with each other and promote pathological processes in endometriosis. METHODS: We analyzed the urine proteome of patients and aimed to detect a potential protein biomarker for endometriosis in the urine proteome. We collected urine samples from 16 patients with endometriosis and 16 patients in the control group with functional ovarian cysts. The diagnosis for all patients was confirmed through pathohistological analysis. After the preanalytical preparation of the urine, chromatography and mass spectrometry (LC-MS/MS) used the technology of urine proteome analysis. RESULTS: The main finding was a significantly different concentration of 14 proteins in the urine samples. We recorded a considerably higher concentration of proteins that have a significant role in activating the immune system (SELL), iron metabolism (HAMP) and cell apoptosis (CHGA) in endometriosis compared to controls. Proteins having an antioxidant function (SOD1) and a role in proteolysis of the extracellular matrix (MMP-9) were significantly reduced in endometriosis compared to controls. CONCLUSION: Consistent with the known pathogenesis of endometriosis, the study results complement the pathological responses that occur with disease progression.
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Introduction

Endometriosis is a chronic inflammatory disease that leads to a series of pathological reactions. The basis is a changed proinflammatory activated immune system, which results in more pronounced oxidative stress, disturbed function of proteolysis and cell apoptosis. These processes are crucial in the development of the disease because their dysfunctional activities cause the progression of the disease. It is believed that the proteins excreted in the urine interact with each other and promote pathological processes in endometriosis.

Methods

We analyzed the urine proteome of patients and aimed to detect a potential protein biomarker for endometriosis in the urine proteome. We collected urine samples from 16 patients with endometriosis and 16 patients in the control group with functional ovarian cysts. The diagnosis for all patients was confirmed through pathohistological analysis. After the preanalytical preparation of the urine, chromatography and mass spectrometry (LC-MS/MS) used the technology of urine proteome analysis.

Results

The main finding was a significantly different concentration of 14 proteins in the urine samples. We recorded a considerably higher concentration of proteins that have a significant role in activating the immune system (SELL), iron metabolism (HAMP) and cell apoptosis (CHGA) in endometriosis compared to controls. Proteins having an antioxidant function (SOD1) and a role in proteolysis of the extracellular matrix (MMP-9) were significantly reduced in endometriosis compared to controls.

Conclusion

Consistent with the known pathogenesis of endometriosis, the study results complement the pathological responses that occur with disease progression. CONFLICT OF INTEREST STATEMENT All authors declare that they have no conflicts of interest that are detrimental to the impartiality of the published research. DATA AVAILABILITY STATEMENT The authors confirm that the data supporting the findings of this study are available within the article and Table 1. Supporting Information | Filename | Description | |---|---| | aji13856-sup-0001-SuppMat.docx37.5 KB | Supporting Information | Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

References

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