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Serum and glucocorticoid inducible protein kinases (SGKs): a potential target for cancer intervention
The serum and glucocorticoid inducible protein kinase (SGK) family members share similar structure, substrate specificity and function with AKT and signal downstream of the phosphatidylinositol 3-kinase (PI3K) signalling pathway. They regulate a range of fundamental cellular processes such as cell p...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146383/ https://www.ncbi.nlm.nih.gov/pubmed/30245963 http://dx.doi.org/10.1016/j.apsb.2018.07.001 |
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author | Basnet, Rajesh Gong, Grace Qun Li, Chenyao Wang, Ming-Wei |
author_facet | Basnet, Rajesh Gong, Grace Qun Li, Chenyao Wang, Ming-Wei |
author_sort | Basnet, Rajesh |
collection | PubMed |
description | The serum and glucocorticoid inducible protein kinase (SGK) family members share similar structure, substrate specificity and function with AKT and signal downstream of the phosphatidylinositol 3-kinase (PI3K) signalling pathway. They regulate a range of fundamental cellular processes such as cell proliferation and survival, thereby playing an important role in cancer development. This perspective intends to give an overview on the involvement of SGKs (particularly SGK3) in cancer progression, and compares the actions of SGK3 and AKT in cell cycle regulation, oncogenic signalling, and the potential as a therapeutic target for cancer. |
format | Online Article Text |
id | pubmed-6146383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-61463832018-09-21 Serum and glucocorticoid inducible protein kinases (SGKs): a potential target for cancer intervention Basnet, Rajesh Gong, Grace Qun Li, Chenyao Wang, Ming-Wei Acta Pharm Sin B Perspective The serum and glucocorticoid inducible protein kinase (SGK) family members share similar structure, substrate specificity and function with AKT and signal downstream of the phosphatidylinositol 3-kinase (PI3K) signalling pathway. They regulate a range of fundamental cellular processes such as cell proliferation and survival, thereby playing an important role in cancer development. This perspective intends to give an overview on the involvement of SGKs (particularly SGK3) in cancer progression, and compares the actions of SGK3 and AKT in cell cycle regulation, oncogenic signalling, and the potential as a therapeutic target for cancer. Elsevier 2018-09 2018-07-05 /pmc/articles/PMC6146383/ /pubmed/30245963 http://dx.doi.org/10.1016/j.apsb.2018.07.001 Text en © 2018 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Perspective Basnet, Rajesh Gong, Grace Qun Li, Chenyao Wang, Ming-Wei Serum and glucocorticoid inducible protein kinases (SGKs): a potential target for cancer intervention |
title | Serum and glucocorticoid inducible protein kinases (SGKs): a potential target for cancer intervention |
title_full | Serum and glucocorticoid inducible protein kinases (SGKs): a potential target for cancer intervention |
title_fullStr | Serum and glucocorticoid inducible protein kinases (SGKs): a potential target for cancer intervention |
title_full_unstemmed | Serum and glucocorticoid inducible protein kinases (SGKs): a potential target for cancer intervention |
title_short | Serum and glucocorticoid inducible protein kinases (SGKs): a potential target for cancer intervention |
title_sort | serum and glucocorticoid inducible protein kinases (sgks): a potential target for cancer intervention |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146383/ https://www.ncbi.nlm.nih.gov/pubmed/30245963 http://dx.doi.org/10.1016/j.apsb.2018.07.001 |
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