作者: Fumihiko Hakuno , Toshiaki Fukushima , Yosuke Yoneyama , Hiroyasu Kamei , Atsufumi Ozoe
关键词: Receptor tyrosine kinase 、 Endocrinology 、 Insulin-like growth factor 、 Insulin 、 IRS2 、 Insulin-like growth factor 1 receptor 、 Insulin receptor substrate 、 Biology 、 Insulin receptor 、 Cell biology 、 GRB10 、 Internal medicine
摘要: Insulin-like peptides, such as insulin-like growth factors (IGFs) and insulin, induce a variety of bioactivities, growth, differentiation, survival, increased anabolism, decreased catabolism in many cell types vivo. In general, IGFs or insulin bind to IGF-I receptor (IGF-IR) (IR), activating the tyrosine kinase. Insulin substrates (IRSs) are known be major kinases, mediating IGF/insulin signals direct bioactivities. Recently, we discovered that IRSs form high-molecular-mass complexes (referred here IRSomes) even without stimulation. These contain proteins IRSAPs; IRS-associated proteins), which modulate phosphorylation by control IRS stability, determine intracellular localization IRSs. addition, these complexes, found not only involved RNA metabolism but also RNAs themselves. Thus, IRSAPs possibly contribute modulation Since it is established disorder activities causes various age-related diseases including cancer, could propose IRSome an important target for treatment diseases.