Literature DB >> 20858173

Sirtuin family: a link to metabolic signaling and senescence.

S Kyrylenko1, A Baniahmad.   

Abstract

A vast collection of data obtained during the last decade supports the view on sirtuins as sensors of actual cellular metabolic state being involved in cell cycle progression, apoptosis/survival decision making, longevity, inflammation etc. Moreover, sirtuins themselves can control metabolism through their ability to consume NAD(+). In turn, cellular NAD parameters may affect the generation of ATP, a main cellular currency of energy. Therefore, sirtuins became recognized as critical affectors of cellular metabolism which participate in fat mobilization, gluconeogenesis, caloric restriction etc. Cellular senescence is viewed as a mechanism to restrict excessive cell growth when it is unnecessary or harmful. It is therefore necessary to understand the mechanism of senescence to design new approaches to combat cancer. Growth in turn depends on metabolism as it requires energy. Therefore, in this review, we address the connection of sirtuins to senescence through their participation in the regulation of metabolic and biochemical parameters and related signaling.

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Year:  2010        PMID: 20858173     DOI: 10.2174/092986710792065009

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  10 in total

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3.  The NAD(+) salvage pathway modulates cancer cell viability via p73.

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Review 6.  Impact of caloric and dietary restriction regimens on markers of health and longevity in humans and animals: a summary of available findings.

Authors:  John F Trepanowski; Robert E Canale; Kate E Marshall; Mohammad M Kabir; Richard J Bloomer
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7.  Mitochondria-ros crosstalk in the control of cell death and aging.

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8.  Alpha-synuclein-induced mitochondrial dysfunction is mediated via a sirtuin 3-dependent pathway.

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9.  Anti-inflammatory effects of concentrated ethanol extracts of Edelweiss (Leontopodium alpinum Cass.) callus cultures towards human keratinocytes and endothelial cells.

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Journal:  Mediators Inflamm       Date:  2012-10-10       Impact factor: 4.711

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  10 in total

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