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. 2020 Sep 18;20(5):255. doi: 10.3892/ol.2020.12118

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Copyright: © Li et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 5. — Enrichment plots from gene set enrichment analysis. (A) VEGF pathway, (B) PTEN pathway, (C) PDGF pathway, (D) ATR and BRCA pathway, (E) CARM and ER pathway, (F) DNA repair, (G) KRAS signaling pathway, (H) PI3K-AKT-mTOR signaling pathway, and (I) the G2M checkpoint were differentially enriched in SCGB2A1-associated uterine corpus endometrial carcinoma. VEGF, vascular endothelial growth factor; PDGF, platelet-derived growth factor; ATR, ataxia-telangiectasia and Rad3-related; CARM, coactivator associated arginine methyltransferase; ER, estrogen receptor; SCGB2A1, secretoglobin family 2A member 1.