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IGF-1 displays more binding sites for SHP2 (a phosphatase related to growth) and seems more prone to recruit Cbl [121] (an E3 ligase that targets the receptor for ubiquitination and destruction) and thus may explain a different regulatory mechanism not mediated by serine phosphorylation, and thus not so sensitive to metabolic derangements
BPC-157 modulates the VEGFR2 pathway to promote angiogenesis, activates the FAK-paxillin system to enhance cell migration toward injury sites, and influences nitric oxide production for improved blood flow
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