Activation of Polyamine Catabolism by N<sup>1</sup>,N<sup>11</sup>-Diethylnorspermine in Hepatic HepaRG Cells Induces Dedifferentiation and Mesenchymal-Like Phenotype
Tumorigenesis is accompanied by the metabolic adaptation of cells to support enhanced proliferation rates and to optimize tumor persistence and amplification within the local microenvironment. In particular, cancer cells exhibit elevated levels of biogenic polyamines. Inhibitors of polyamine biosynt...
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doaj-ea67aed7265e479cb82b5746ed3972ce2020-11-25T01:41:04ZengMDPI AGCells2073-44092018-12-0171227510.3390/cells7120275cells7120275Activation of Polyamine Catabolism by N<sup>1</sup>,N<sup>11</sup>-Diethylnorspermine in Hepatic HepaRG Cells Induces Dedifferentiation and Mesenchymal-Like PhenotypeOlga N. Ivanova0Anastasiya V. Snezhkina1George S. Krasnov2Vladimir T. Valuev-Elliston3Olga A. Khomich4Alexey R. Khomutov5Tuomo A. Keinanen6Leena Alhonen7Birke Bartosch8Anna V. Kudryavtseva9Sergey N. Kochetkov10Alexander V. Ivanov11Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, RussiaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, RussiaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, RussiaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, RussiaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, RussiaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, RussiaSchool of Pharmacy, Biocenter Kuopio, University of Eastern Finland, FI-70211 Kuopio, FinlandSchool of Pharmacy, Biocenter Kuopio, University of Eastern Finland, FI-70211 Kuopio, FinlandCancer Research Center Lyon, INSERM U1052 and CNRS 5286, Lyon University, 69000 Lyon, FranceEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, RussiaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, RussiaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, RussiaTumorigenesis is accompanied by the metabolic adaptation of cells to support enhanced proliferation rates and to optimize tumor persistence and amplification within the local microenvironment. In particular, cancer cells exhibit elevated levels of biogenic polyamines. Inhibitors of polyamine biosynthesis and inducers of their catabolism have been evaluated as antitumor drugs, however, their efficacy and safety remain controversial. Our goal was to investigate if drug-induced modulation of polyamine metabolism plays a role in dedifferentiation using differentiated human hepatocyte-like HepaRG cell cultures. N<sup>1</sup>,N<sup>11</sup>-diethylnorspermine (DENSpm), a potent inducer of polyamine catabolism, triggered an epithelial-mesenchymal transition (EMT)-like dedifferentiation in HepaRG cultures, as shown by down-regulation of mature hepatocytes markers and upregulation of classical EMT markers. Albeit the fact that polyamine catabolism produces H2O2, DENSpm-induced de-differentiation was not affected by antioxidants. Use of a metabolically stable spermidine analogue showed furthermore, that spermidine is a key regulator of hepatocyte differentiation. Comparative transcriptome analyses revealed, that the DENSpm-triggered dedifferentiation of HepaRG cells was accompanied by dramatic metabolic adaptations, exemplified by down-regulation of the genes of various metabolic pathways and up-regulation of the genes involved in signal transduction pathways. These results demonstrate that polyamine metabolism is tightly linked to EMT and differentiation of liver epithelial cells.https://www.mdpi.com/2073-4409/7/12/275polyaminesHepaRGpolyamine catabolismdedifferentiationEMTspermidinepolyamine analoguesNextSeqhepatocytes |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Olga N. Ivanova Anastasiya V. Snezhkina George S. Krasnov Vladimir T. Valuev-Elliston Olga A. Khomich Alexey R. Khomutov Tuomo A. Keinanen Leena Alhonen Birke Bartosch Anna V. Kudryavtseva Sergey N. Kochetkov Alexander V. Ivanov |
spellingShingle |
Olga N. Ivanova Anastasiya V. Snezhkina George S. Krasnov Vladimir T. Valuev-Elliston Olga A. Khomich Alexey R. Khomutov Tuomo A. Keinanen Leena Alhonen Birke Bartosch Anna V. Kudryavtseva Sergey N. Kochetkov Alexander V. Ivanov Activation of Polyamine Catabolism by N<sup>1</sup>,N<sup>11</sup>-Diethylnorspermine in Hepatic HepaRG Cells Induces Dedifferentiation and Mesenchymal-Like Phenotype Cells polyamines HepaRG polyamine catabolism dedifferentiation EMT spermidine polyamine analogues NextSeq hepatocytes |
author_facet |
Olga N. Ivanova Anastasiya V. Snezhkina George S. Krasnov Vladimir T. Valuev-Elliston Olga A. Khomich Alexey R. Khomutov Tuomo A. Keinanen Leena Alhonen Birke Bartosch Anna V. Kudryavtseva Sergey N. Kochetkov Alexander V. Ivanov |
author_sort |
Olga N. Ivanova |
title |
Activation of Polyamine Catabolism by N<sup>1</sup>,N<sup>11</sup>-Diethylnorspermine in Hepatic HepaRG Cells Induces Dedifferentiation and Mesenchymal-Like Phenotype |
title_short |
Activation of Polyamine Catabolism by N<sup>1</sup>,N<sup>11</sup>-Diethylnorspermine in Hepatic HepaRG Cells Induces Dedifferentiation and Mesenchymal-Like Phenotype |
title_full |
Activation of Polyamine Catabolism by N<sup>1</sup>,N<sup>11</sup>-Diethylnorspermine in Hepatic HepaRG Cells Induces Dedifferentiation and Mesenchymal-Like Phenotype |
title_fullStr |
Activation of Polyamine Catabolism by N<sup>1</sup>,N<sup>11</sup>-Diethylnorspermine in Hepatic HepaRG Cells Induces Dedifferentiation and Mesenchymal-Like Phenotype |
title_full_unstemmed |
Activation of Polyamine Catabolism by N<sup>1</sup>,N<sup>11</sup>-Diethylnorspermine in Hepatic HepaRG Cells Induces Dedifferentiation and Mesenchymal-Like Phenotype |
title_sort |
activation of polyamine catabolism by n<sup>1</sup>,n<sup>11</sup>-diethylnorspermine in hepatic heparg cells induces dedifferentiation and mesenchymal-like phenotype |
publisher |
MDPI AG |
series |
Cells |
issn |
2073-4409 |
publishDate |
2018-12-01 |
description |
Tumorigenesis is accompanied by the metabolic adaptation of cells to support enhanced proliferation rates and to optimize tumor persistence and amplification within the local microenvironment. In particular, cancer cells exhibit elevated levels of biogenic polyamines. Inhibitors of polyamine biosynthesis and inducers of their catabolism have been evaluated as antitumor drugs, however, their efficacy and safety remain controversial. Our goal was to investigate if drug-induced modulation of polyamine metabolism plays a role in dedifferentiation using differentiated human hepatocyte-like HepaRG cell cultures. N<sup>1</sup>,N<sup>11</sup>-diethylnorspermine (DENSpm), a potent inducer of polyamine catabolism, triggered an epithelial-mesenchymal transition (EMT)-like dedifferentiation in HepaRG cultures, as shown by down-regulation of mature hepatocytes markers and upregulation of classical EMT markers. Albeit the fact that polyamine catabolism produces H2O2, DENSpm-induced de-differentiation was not affected by antioxidants. Use of a metabolically stable spermidine analogue showed furthermore, that spermidine is a key regulator of hepatocyte differentiation. Comparative transcriptome analyses revealed, that the DENSpm-triggered dedifferentiation of HepaRG cells was accompanied by dramatic metabolic adaptations, exemplified by down-regulation of the genes of various metabolic pathways and up-regulation of the genes involved in signal transduction pathways. These results demonstrate that polyamine metabolism is tightly linked to EMT and differentiation of liver epithelial cells. |
topic |
polyamines HepaRG polyamine catabolism dedifferentiation EMT spermidine polyamine analogues NextSeq hepatocytes |
url |
https://www.mdpi.com/2073-4409/7/12/275 |
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