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With the therapy done immediately after wounding, we performed the Akt1, Braf, Egfr, Egr1, Grb2, Hdac7, Kras, Mapk1, Mapk3, Mapk14, Nos3, Pik3cd, Plcg1, Prkcg, Ptk2, Pxn, Src, Srf , and Vegfa genes expression analysis in the rats excision wounds, in the skin, and subcutaneous tissue, done at 2, 5, and 10 min following BPC 157 application (Figure 8)

The results demonstrated a significant reduction in IRES-driven luciferase activity following SYNCRIP depletion, further supporting the idea that SYNCRIP facilitates cap-independent translation of HK2 mRNA (Figure 6F-H)