Ras signaling in aging and metabolic regulation

Abstract

Aberrant signal transduction downstream of the Ras GTPase has a well-established role in tumorigenesis. Mutations that result in hyperactivation of Ras are responsible for a third of all human cancers. Hence, small molecule inhibitors of the Ras signal transduction cascade have been under intense focus as potential cancer treatments. In both invertebrate and mammalian models, emerging evidence has also implicated components of the Ras signaling pathway in aging and metabolic regulation. Here, I review the current evidence for Ras signaling in these newly discovered roles highlighting the interactions between the Ras pathway and other longevity assurance mechanisms. Defining the role of Ras signaling in maintaining age-related health may have important implications for the development of interventions that could not only increase lifespan but also delay the onset and/or progression of age-related functional decline.

Publication DOI: https://doi.org/10.3233/NHA-160021
Divisions: College of Health & Life Sciences
College of Health & Life Sciences > School of Biosciences > Cell & Tissue Biomedical Research
Funding Information: The author would like to thank Nazif Alic for critical reading of the manuscript. The author is currently supported by an internal start-up award given by the School of Life and Health Sciences, Aston University.
Additional Information: © 2017 – IOS Press and the authors. This article is published online with Open Access and distributed under the terms of the Creative Commons Attribution Non-Commercial License (CC BY-NC 4.0)
Uncontrolled Keywords: aging,Lifespan,metabolism,Ras signaling,Food Science,Biochemistry,Medicine (miscellaneous),Nutrition and Dietetics
Publication ISSN: 2451-9502
Last Modified: 25 Mar 2024 08:26
Date Deposited: 09 Apr 2018 09:25
Full Text Link:
Related URLs: http://www.scop ... tnerID=8YFLogxK (Scopus URL)
https://content ... aging/nha160021 (Publisher URL)
PURE Output Type: Review article
Published Date: 2017-12-07
Accepted Date: 2017-12-01
Authors: Slack, Cathy (ORCID Profile 0000-0002-7949-4079)

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