Abstract
Purpose
To investigate the potential role of Bone morphogenetic protein 1 (BMP1) in endometriosis lesions.
Methods
Endometriosis model in mice was established. The expression of BMP1-3 expression in mice of endometriosis lesions was evaluated. The effect of the treatment with anti-BMP1 antibodies on the expression of MMP2, MMP9, TGF-β, IL-17, IL-1β, Col1a1 and Col1a2 levels in mice was evaluated. In endometriosis cell model, the expression of IL-17, IL-1β, MMP2 and MMP9 levels and MIF, YWHAZ, β-catenin and CAP39 mRNA levels was also detected.
Results
The expression of BMP1-3 expression was upregulated in mice of endometriosis lesions (p < 0.01). Treatment with anti-BMP1 antibodies dose-dependently reduced MMP2, MMP9, TGF-β, IL-17, IL-1β, Col1a1 and Col1a2 levels in mice (p < 0.01). Treatment with anti-BMP1 antibodies suppressed TGF-β/PI3K/Akt signaling pathway. In vitro cell, si-BMP1 suppressed TGF-β/PI3K/Akt signaling pathway.
Conclusion
The data support the hypothesis that the inhibition of BMP1 is involved in the pathogenesis of endometriosis lesions.
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WW carried out the study concepts; XH, WW were dedicated to the study design, literature research and manuscript review; XH was involved in the definition of intellectual content, experimental studies, data analysis, manuscript preparation and manuscript editing; XH and FH were dedicated to clinical studies; XH, FH and FC carried out the data acquisition; FH and FC were involved in the statistical analysis. All authors have read and approved this article.
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This study was carried out in accordance with recommendations of the regulations for animal experimentation in Hyogo College of Medicine of The University of Hong Kong-Shenzhen Hospital.
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Han, X., Hu, F., Chen, F. et al. The inhibition of bone morphogenetic protein 1 attenuates endometriosis lesions in vivo and in vitro. Arch Gynecol Obstet 302, 415–422 (2020). https://doi.org/10.1007/s00404-020-05612-4
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DOI: https://doi.org/10.1007/s00404-020-05612-4