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Recent advances in PTP1B signaling in metabolism and cancer.
Villamar-Cruz, Olga; Loza-Mejía, Marco A; Arias-Romero, Luis E; Camacho-Arroyo, Ignacio.
Afiliação
  • Villamar-Cruz O; Unidad de Investigación en Reproducción Humana, Instituto Nacional de Perinatología-Facultad de Química, Universidad Nacional Autónoma de México (UNAM), Ciudad de México, Mexico.
  • Loza-Mejía MA; Unidad de Investigación en Biomedicina (UBIMED), Facultad de Estudios Superiores-Iztacala, UNAM. Tlalnepantla, Estado de México 54090, Mexico.
  • Arias-Romero LE; Facultad de Ciencias Químicas, Universidad La Salle-México. Benjamin Franklin 45 06140, Mexico City, Mexico.
  • Camacho-Arroyo I; Unidad de Investigación en Biomedicina (UBIMED), Facultad de Estudios Superiores-Iztacala, UNAM. Tlalnepantla, Estado de México 54090, Mexico.
Biosci Rep ; 41(11)2021 11 26.
Article em En | MEDLINE | ID: mdl-34726241
ABSTRACT
Protein tyrosine phosphorylation is one of the major post-translational modifications in eukaryotic cells and represents a critical regulatory mechanism of a wide variety of signaling pathways. Aberrant protein tyrosine phosphorylation has been linked to various diseases, including metabolic disorders and cancer. Few years ago, protein tyrosine phosphatases (PTPs) were considered as tumor suppressors, able to block the signals emanating from receptor tyrosine kinases. However, recent evidence demonstrates that misregulation of PTPs activity plays a critical role in cancer development and progression. Here, we will focus on PTP1B, an enzyme that has been linked to the development of type 2 diabetes and obesity through the regulation of insulin and leptin signaling, and with a promoting role in the development of different types of cancer through the activation of several pro-survival signaling pathways. In this review, we discuss the molecular aspects that support the crucial role of PTP1B in different cellular processes underlying diabetes, obesity and cancer progression, and its visualization as a promising therapeutic target.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Proteína Tirosina Fosfatase não Receptora Tipo 1 / Doenças Metabólicas / Neoplasias Tipo de estudo: Etiology_studies Limite: Animals / Humans Idioma: En Revista: Biosci Rep Ano de publicação: 2021 Tipo de documento: Article País de afiliação: México

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Proteína Tirosina Fosfatase não Receptora Tipo 1 / Doenças Metabólicas / Neoplasias Tipo de estudo: Etiology_studies Limite: Animals / Humans Idioma: En Revista: Biosci Rep Ano de publicação: 2021 Tipo de documento: Article País de afiliação: México