Insulinum quasi incrementum factor 2 (IGF2) hormona dapibus notum est cellam multiplicationem moderari, incrementum, migratio, differentiam et salvos. Genea parentaliter imprimitur in sensu qui transcripta fere unice ex allele paternis derivantur. Amissio impressionis generum IGF2 est observatio recurrentis in perturbationibus incrementi quae cum variis tumoribus malignorum malignorum cohaerent excrescentia. Praeterea, IGF2 has been proposed to play a role in the development of a variety of seemingly unrelated cancers that play an important role in geriatric medicine, e.g*. pectus cancer, colon cancer and lung cancer. denique, IGF2 has been implicated in cardiovascular disease, since, exempli gratia, IGF2 has been shown to influence the size of atherosclerotic lesions.
IGF2 is a crucial factor for the regulation of cell proliferation, incrementum, migratio, differentiam et salvos. IGF2 (as well as IGF1) interacts with several receptors and binding proteins in order to exert its actions. It binds to the non-signaling IGF type 2 receptor (IGF2R) with high affinity. This receptor is homologous to the cation-independent mannose-6-phosphate (M6P) receptor. IGF2 can also bind to different signaling receptors, such as the IGF type 1 receptor (IGF1R) et receptor insulinum, albeit with lower affinity, although an alternatively spliced version of the insulin receptor, named insulin receptor isoform A, may bind IGF2 with higher affinity.
Both IGF1 and IGF2 are present in the circulation and can be readily detected in plasma. As might be predicted from the pattern of synthesis, circulating IGF1 levels rise during juvenile life and then decline after puberty, while circulating IGF2 levels are highest in the fetal circulation. Circulating IGFs are mostly associated with 6 specifically designed binding proteins (IGFBPs) which exhibit tissue- and stage-specific expression. In vitro, all IGFBPs inhibit the biological activity of IGFs, suggesting that part of their function may be to restrict the availability of biologically active IGFs
