Potential Role of Insulin Growth-Factor-Binding Protein 2 as Therapeutic Target for Obesity-Related Insulin Resistance

Evidence from observational and in vitro studies suggests that insulin growth-factor-binding protein type 2 (IGFBP2) is a promising protein in non-communicable diseases, such as obesity, insulin resistance, metabolic syndrome, or type 2 diabetes. Accordingly, great efforts have been carried out to e...

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Detalles Bibliográficos
Autores: Boughanem, Hatim, Yubero-Serrano, Elena M., López-Miranda, José, Tinahones, Francisco J., Macias-Gonzalez, Manuel
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Instituto de Salud Carlos III (ISCIII)
Repositorio:Repisalud
Idioma:inglés
OAI Identifier:oai:repisalud.isciii.es:20.500.12105/18239
Acceso en línea:http://hdl.handle.net/20.500.12105/18239
Access Level:acceso abierto
Palabra clave:IGFBP2
Obesity
Insulin resistance
Lifestyle modification
Epigenetic
Proteína 2 de unión a factor de crecimiento similar a la insulina
Obesidad
Resistencia a la insulina
Estilo de vida
Epigénesis genética
Diabetes Mellitus, Type 2
Humans
Insulin-Like Growth Factor Binding Protein 2
Insulin Resistance
Quality of Life
Molecular Structure
Exercise
Diet
Descripción
Sumario:Evidence from observational and in vitro studies suggests that insulin growth-factor-binding protein type 2 (IGFBP2) is a promising protein in non-communicable diseases, such as obesity, insulin resistance, metabolic syndrome, or type 2 diabetes. Accordingly, great efforts have been carried out to explore the role of IGFBP2 in obesity state and insulin-related diseases, which it is typically found decreased. However, the physiological pathways have not been explored yet, and the relevance of IGFBP2 as an important pathway integrator of metabolic disorders is still unknown. Here, we review and discuss the molecular structure of IGFBP2 as the first element of regulating the expression of IGFBP2. We highlight an update of the association between low serum IGFBP2 and an increased risk of obesity, type 2 diabetes, metabolic syndrome, and low insulin sensitivity. We hypothesize mechanisms of IGFBP2 on the development of obesity and insulin resistance in an insulin-independent manner, which meant that could be evaluated as a therapeutic target. Finally, we cover the most interesting lifestyle modifications that regulate IGFBP2, since lifestyle factors (diet and/or physical activity) are associated with important variations in serum IGFBP2.