Glycogen synthase kinase 3β in tumorigenesis and oncotherapy (Review)

Autor: Tiantian Lei, Yi Wang, Xiaofang Xie, Rui He, Suya Du
Rok vydání: 2020
Předmět:
0301 basic medicine
Cancer Research
oncotherapy
Carcinogenesis
Cellular differentiation
GSK 3β inhibitors
Cell
Apoptosis
Review
macromolecular substances
Biology
medicine.disease_cause
Mice
03 medical and health sciences
Antineoplastic Agents
Immunological

0302 clinical medicine
GSK-3
Neoplasms
Antineoplastic Combined Chemotherapy Protocols
medicine
Animals
Humans
Lymphocytes
Phosphorylation
Protein Kinase Inhibitors
Glycogen Synthase Kinase 3 beta
Oncogene
Kinase
Cell growth
General Medicine
Cell cycle
Gene Expression Regulation
Neoplastic

Disease Models
Animal

tumorigenesis
glycogen synthase kinase 3β
030104 developmental biology
medicine.anatomical_structure
Oncology
030220 oncology & carcinogenesis
Proteolysis
Disease Progression
Cancer research
Signal Transduction
Transcription Factors
Zdroj: Oncology Reports
ISSN: 1791-2431
1021-335X
DOI: 10.3892/or.2020.7817
Popis: Glycogen synthase kinase 3β (GSK 3β), a multifunctional serine and threonine kinase, plays a critical role in a variety of cellular activities, including signaling transduction, protein and glycogen metabolism, cell proliferation, cell differentiation, and apoptosis. Therefore, aberrant regulation of GSK 3β results in a broad range of human diseases, such as tumors, diabetes, inflammation and neurodegenerative diseases. Accumulating evidence has suggested that GSK 3β is correlated with tumorigenesis and progression. However, GSK 3β is controversial due to its bifacial roles of tumor suppression and activation. In addition, overexpression of GSK 3β is involved in tumor growth, whereas it contributes to the cell sensitivity to chemotherapy. However, the underlying regulatory mechanisms of GSK 3β in tumorigenesis remain obscure and require further in-depth investigation. In this review, we comprehensively summarize the roles of GSK 3β in tumorigenesis and oncotherapy, and focus on its potentials as an available target in oncotherapy.
Databáze: OpenAIRE