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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Main Authors: 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
Format: Article
Language:English
Published: MDPI AG 2018-12-01
Series:Cells
Subjects:
EMT
Online Access:https://www.mdpi.com/2073-4409/7/12/275
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spelling 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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