| Literature DB >> 26003731 |
Ritu Malla1, Charles R Ashby2, Narayanan K Narayanan3, Bhagavathi Narayanan3, Jesika S Faridi4, Amit K Tiwari5.
Abstract
Dysregulation of PI3K-AKT-mTOR pathway has been reported in various pathologies, such as cancer and insulin resistance. The proline-rich AKT substrate of 40-kDa (PRAS40), also known as AKT substrate 1 (AKT1S1), lies at the crossroads of these cascades and inhibits the activity of the mTOR complex 1 (mTORC1) kinase. This review discusses the role of PRAS40 and possible feedback mechanisms, and alterations in AKT/PRAS40/mTOR signaling that have been implicated in the pathogenesis of tumor progression. Additionally, we probed new datasets extracted from Oncomine, a cancer microarray database containing datasets derived from patient samples, to further understand the role of PRAS40 (AKT1S1). These data strongly supports the hypothesis that PRAS40 may serve as a potential therapeutic target for various cancers.Entities:
Keywords: Cancer therapeutics; PI3K/AKT; PRAS40; mTORC1
Mesh:
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Year: 2015 PMID: 26003731 DOI: 10.1016/j.bbrc.2015.05.041
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575