Literature DB >> 25818187

The S6K protein family in health and disease.

Mariana R Tavares1, Isadora C B Pavan1, Camila L Amaral1, Letícia Meneguello2, Augusto D Luchessi2, Fernando M Simabuco3.   

Abstract

The S6K proteins are mTOR pathway effectors and accumulative evidence suggest that mTOR/S6K signaling contributes to several pathological conditions, such as diabetes, cancer and obesity. The activation of the mTOR/S6K axis stimulates protein synthesis and cell growth. S6K1 has two well-known isoforms, p70-S6K1 and p85-S6K1, generated by alternative translation initiation sites. A third isoform, named p31-S6K1, has been characterized as a truncated type of the protein due to alternative splicing, and reports have shown its important role in cancer. Studies involving S6K2 are scarce. This article aims to review what is new in the literature about these kinases and establish differences regarding their interacting proteins, activation and function, connecting their roles in the homeostasis of the cell and in pathological conditions.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cancer; Diabetes; Metabolism; Obesity; S6K1; S6K2; mTOR

Mesh:

Substances:

Year:  2015        PMID: 25818187     DOI: 10.1016/j.lfs.2015.03.001

Source DB:  PubMed          Journal:  Life Sci        ISSN: 0024-3205            Impact factor:   5.037


  81 in total

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5.  Modulation of hypothalamic S6K1 and S6K2 alters feeding behavior and systemic glucose metabolism.

Authors:  Mariana Rosolen Tavares; Simone Ferreira Lemes; Thais de Fante; Cristina Saenz de Miera; Isadora Carolina Betim Pavan; Rosangela Maria Neves Bezerra; Patricia Oliveira Prada; Marcio Alberto Torsoni; Carol Fuzeti Elias; Fernando Moreira Simabuco
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Review 10.  Mammalian target of rapamycin complex (mTOR) pathway modulates blood-testis barrier (BTB) function through F-actin organization and gap junction.

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