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10.1111/1471-0528.14689 23 ChengI

ectopic and eutopic endometrium tissue samples were taken from each participant during laparoscopy The samples underwent peptide extraction, peptide purification, peptide desalting and TMT labeling Analyses were done by Liquid chromatography (LC)-tandem mass spectrometry techniques Bioinformatics was used to determine the peptide-protein precursor functions Highly differentiated endometrial stromal cells (ESC) obtained and cultured, then subject to wound healing assays, to illuminate migration patterns in the presence of the above peptides Transwell assays were used to determine the invasive properties of some cells The data was subject to statistical analysis

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demonstrated that IGF-1 reduced atrogin-1 expression within 1 hour by blocking mRNA synthesis, with MuRF1 suppression following more gradually