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Journal of Applied Toxicology (2011)

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The binding of IGFs to their receptors activates both MAPK and PI3K-AKT pathways, which results in downstream cellular effects (such as cellular proliferation, anti-apoptosis, and differentiation actions) through other downstream molecules ( IRS 1-4 and other signaling proteins, such as Shc, bind to the IGF-1R at the extracellular subunit as a result of the binding of IGF-I and IGF-II ( Recent research has shown that the IGF-1R (and IR) can migrate to the nucleus in both healthy and cancerous cells through mechanisms that are still being fully elucidated, although sumoylation is thought to be one method

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