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S‐Adenosylmethionine: a control switch that regulates liver function
Open accessAbstract
Genome sequence analysis reveals that all organisms synthesize S‐adenosylmethionine (AdoMet) and that a large fraction of all genes is AdoMet‐dependent methyltransferases. AdoMet‐dependent methylation has been shown to be central to many biological processes. Up to 85% of all methylation reactions and as much as 48% of methionine metabo‐lism occur in the liver, which indicates the crucial importance of this organ in the regulation of blood methionine. Of the two mammalian genes (MAT1A, MAT2A ) that encode methionine adenosyltransferase (MAT, the enzyme that makes AdoMet), MAT1A is specifically expressed in adult liver. It now appears that growth factors, cytokines, and hormones regulate liver MAT mRNA levels and enzyme activity and that AdoMet should not be viewed only as an intermediate metabolite in methionine catabolism, but also as an intracellular control switch that regulates essential he‐patic functions such as regeneration, differentiation, and the sensitivity of this organ to injury. The aim of this review is to integrate these recent findings linking AdoMet with liver growth, differentiation, and injury into a comprehensive model. With the availability of AdoMet as a nutritional supplement and evidence of its beneficial role in various liver diseases, this review offers insight into its mechanism of action.—Mato, J. M., Corrales, F. J., Lu, S. C., Avila, M. A. S‐Adenosylmethionine: a control switch that regulates liver function. FASEB J. 16, 15–26 (2002)
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Cites
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Cheung, P., Allis, C. D., & Sassone-Corsi, P. (2000) · Cell · doi:10.1016/s0092-8674(00)00118-5 · Cited by 989
Cytochrome P-4502E1: its physiological and pathological role
Lieber, C. S. (1997) · Physiological Reviews · doi:10.1152/physrev.1997.77.2.517 · Cited by 889
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Self-citationS-Adenosylmethionine: jack of all trades and master of everything?
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Frau, M., Feo, F., & Pascale, R. M. (2013) · Journal of Hepatology · doi:10.1016/j.jhep.2013.04.031 · Cited by 179
Lo, T.-F., Tsai, W.-C., & Chen, S.-T. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075628 · Cited by 122
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García-Giménez, J. L., Romá-Mateo, C., Pérez-Machado, G., Peiró-Chova, L., & Pallardó, F. V. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.07.008 · Cited by 116
Metadata
- Authors
- Mato, J. M., Corrales, F. J., Lu, S. C., & Avila, M. A.
- Venue
- The FASEB Journal
- Publisher
- Wiley
- Published
- 2002-01
- Volume
- 16
- Issue
- 1
- Pages
- 15-26
- ISSN
- 0892-6638 (ISSN-L)
- 1530-6860
- OpenAlex
- W2018404966
- Cited by
- 426
- References
- 2
- FWCI
- 9.70
- Type
- journal article
- Language
- en
- Open access
- green
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