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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)

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)

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