{"paper_id":"59883bb6-e2b1-4d35-aa3b-e219119672c4","body_text":"Involvement of the Wnt/β-Catenin Signaling Pathway in the Cellular and Molecular Mechanisms of Fibrosis in Endometriosis\nFigure 5\nEffects of CGP049090 treatment on fibrosis in a mouse endometriosis model.\nA-D: Staining score for Sirius Red (A, B) or Masson Trichrome (C, D) staining in a time course study of fibrosis development (on days 0, 7, 14, 21, and 28) (A, C) and vehicle-treated and CGP049090 (2 mg/kg)-treated mice (Groups I and II: treated once a day between days 7 and 21 for 14 days; Groups III and IV: treated once a day between days 14 and 28 for 14 days) (B, D).\n*: p<.05 versus endometrium on day 0 and endometriotic implants on day 7.\n**: p<.05 versus vehicle-treated mice.\nDay 0 (endometrium) (n=10), Days 7 (n=10), 14 (n=10), 21 (n=10), or 28 (n=10).\nV: vehicle-treated mice; T: CGP049090 (2 mg/kg)-treated mice.\nG1: Group I (n=10), GII: Group II (n=10), GIII: Group III (n=10), GIV: Group IV (n=10).\nE-G: Representative photomicrographs of the endometrium stained with hematoxylin and eosin, Sirius Red, or Masson Trichrome on day 0 (E), or of endometriotic implants of mice treated for 14 days with vehicle alone (F) or with CGP049090 (G) at day 21. Scale bars (a-c, g-i, m-o: 200 μm; d-f, j-l, p-r: 50 μm).","source_license":"CC0","license_restricted":false}