Cited by 202Polyamine Metabolism and ApplicationsAmino Acid Enzymes and MetabolismBiochemical effects in animals

Polyamines: fundamental characters in chemistry and biology

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Abstract

Polyamines are small cationic molecules required for cellular proliferation and are detected at higher concentrations in most tumour tissues, compared to normal tissues. Agmatine (AGM), a biogenic amine, is able to arrest proliferation in cell lines by depleting intracellular polyamine levels. It enters mammalian cells via the polyamine transport system. Agmatine is able to induce oxidative stress in mitochondria at low concentrations (10 or 100 microM), while at higher concentrations (e.g. 1-2 mM) it does not affect mitochondrial respiration and is ineffective in inducing any oxidative stress. As this effect is strictly correlated with the mitochondrial permeability transition induction and the triggering of the pro-apoptotic pathway, AGM may be considered as a regulator of this type of cell death. Furthermore, polyamine transport is positively correlated with the rate of cellular proliferation. By increasing the expression of antizyme, a protein that inhibits polyamine biosynthesis and transport, AGM also exhibits a regulatory effect on cell proliferation. Methylglyoxal bis(guanylhydrazone) (MGBG), a competitive inhibitor of S-adenosyl-L: -methionine decarboxylase, displaying anticancer activity, is a structural analogue of the natural polyamine spermidine. MGBG has been extensively studied, preclinically as well as clinically, and its anticancer activity has been attributed to the inhibition of polyamine biosynthesis and also to its effect on mitochondrial function. Numerous findings have suggested that MGBG might be used as a chemotherapeutic agent against cancer.

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  • The MPT response can be blocked by polyamines such as spermine or spermidine, possibly due to their antioxidant effects.

    “Interestingly, in addition to cyclosporine A or bongkrekic, the MPT response can be blocked by polyamines, such as spermine or spermidine, possibly due to their antioxidant effects (5).”

    From Redox regulation of mitochondrial function (2012) · cites this paper as [5]

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Authors
Agostinelli, E., Marques, M. P. M., Calheiros, R., Gil, F. P. S. C., Tempera, G., Viceconte, N., Battaglia, V., Grancara, S., & Toninello, A.
Affiliations
  • National Research Council (IT)
  • University of Coimbra (PT)
  • University of Padua (IT)
Corresponding author
Agostinelli, E.
Venue
Amino Acids
Published
2009-12-15
Volume
38
Issue
2
Pages
393-403
ISSN
  • 0939-4451 (ISSN-L)
  • 1438-2199
OpenAlex
W2167533746
Cited by
202
References
87
Citations by year
2026: 9 · 2025: 7 · 2024: 10 · 2023: 14 · 2022: 8 · 2021: 8 · 2020: 8 · 2019: 13 · 2018: 10 · 2017: 12 · 2016: 11 · 2015: 16 · 2014: 17 · 2013: 15 · 2012: 9
FWCI
1.15
Type
journal article
Language
en
Open access
Locations
  • Amino Acids (publishedVersion)
  • PubMed (publishedVersion)
  • Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) (submittedVersion, other-oa)
  • Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) (submittedVersion)
  • IRIS Research product catalog (Sapienza University of Rome) (submittedVersion)
Funders
  • Ministero dell’Istruzione, dell’Università e della Ricerca
  • Fundação para a Ciência e a Tecnologia (PTDC/QUI/66701/2006)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Polyamine Metabolism and Applications
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
  • Health Sciences › Medicine › Physiology (medical) › Biochemical effects in animals
Keywords
polyamines, agmatine, polyamine transport, antizyme, methylglyoxal bis(guanylhydrazone), S-adenosylmethionine decarboxylase, polyamine biosynthesis inhibition, mitochondrial permeability transition, oxidative stress, apoptosis, cell proliferation, anticancer agents, spermidine
MeSH terms
Agmatine, Animals, Biological Transport, Humans, Mitochondria, Neoplasms, Polyamines, Molecular Structure, Cell Proliferation

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