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Dihydropyridine Derivatives as Cell Growth Modulators In Vitro

The effects of eleven 1,4-dihydropyridine derivatives (DHPs) used alone or together with prooxidant anticancer drug doxorubicin were examined on two cancer (HOS, HeLa) and two nonmalignant cell lines (HMEC, L929). Their effects on the cell growth ((3)H-thymidine incorporation) were compared with the...

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Autores principales: Bruvere, Imanta, Bisenieks, Egils, Poikans, Janis, Uldrikis, Janis, Plotniece, Aiva, Pajuste, Karlis, Rucins, Martins, Vigante, Brigita, Kalme, Zenta, Gosteva, Marina, Domracheva, Ilona, Velena, Astrida, Vukovic, Tea, Milkovic, Lidija, Duburs, Gunars, Zarkovic, Neven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394904/
https://www.ncbi.nlm.nih.gov/pubmed/28473879
http://dx.doi.org/10.1155/2017/4069839
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author Bruvere, Imanta
Bisenieks, Egils
Poikans, Janis
Uldrikis, Janis
Plotniece, Aiva
Pajuste, Karlis
Rucins, Martins
Vigante, Brigita
Kalme, Zenta
Gosteva, Marina
Domracheva, Ilona
Velena, Astrida
Vukovic, Tea
Milkovic, Lidija
Duburs, Gunars
Zarkovic, Neven
author_facet Bruvere, Imanta
Bisenieks, Egils
Poikans, Janis
Uldrikis, Janis
Plotniece, Aiva
Pajuste, Karlis
Rucins, Martins
Vigante, Brigita
Kalme, Zenta
Gosteva, Marina
Domracheva, Ilona
Velena, Astrida
Vukovic, Tea
Milkovic, Lidija
Duburs, Gunars
Zarkovic, Neven
author_sort Bruvere, Imanta
collection PubMed
description The effects of eleven 1,4-dihydropyridine derivatives (DHPs) used alone or together with prooxidant anticancer drug doxorubicin were examined on two cancer (HOS, HeLa) and two nonmalignant cell lines (HMEC, L929). Their effects on the cell growth ((3)H-thymidine incorporation) were compared with their antiradical activities (DPPH assay), using well-known DHP antioxidant diludine as a reference. Thus, tested DHPs belong to three groups: (1) antioxidant diludine; (2) derivatives with pyridinium moieties at position 4 of the 1,4-DHP ring; (3) DHPs containing cationic methylene onium (pyridinium, trialkylammonium) moieties at positions 2 and 6 of the 1,4-DHP ring. Diludine and DHPs of group 3 exerted antiradical activities, unlike compounds of group 2. However, novel DHPs had cell type and concentration dependent effects on (3)H-thymidine incorporation, while diludine did not. Hence, IB-32 (group 2) suppressed the growth of HOS and HeLa, enhancing growth of L929 cells, while K-2-11 (group 3) enhanced growth of every cell line tested, even in the presence of doxorubicin. Therefore, growth regulating and antiradical activity principles of novel DHPs should be further studied to find if DHPs of group 2 could selectively suppress cancer growth and if those of group 3 promote wound healing.
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spelling pubmed-53949042017-05-04 Dihydropyridine Derivatives as Cell Growth Modulators In Vitro Bruvere, Imanta Bisenieks, Egils Poikans, Janis Uldrikis, Janis Plotniece, Aiva Pajuste, Karlis Rucins, Martins Vigante, Brigita Kalme, Zenta Gosteva, Marina Domracheva, Ilona Velena, Astrida Vukovic, Tea Milkovic, Lidija Duburs, Gunars Zarkovic, Neven Oxid Med Cell Longev Research Article The effects of eleven 1,4-dihydropyridine derivatives (DHPs) used alone or together with prooxidant anticancer drug doxorubicin were examined on two cancer (HOS, HeLa) and two nonmalignant cell lines (HMEC, L929). Their effects on the cell growth ((3)H-thymidine incorporation) were compared with their antiradical activities (DPPH assay), using well-known DHP antioxidant diludine as a reference. Thus, tested DHPs belong to three groups: (1) antioxidant diludine; (2) derivatives with pyridinium moieties at position 4 of the 1,4-DHP ring; (3) DHPs containing cationic methylene onium (pyridinium, trialkylammonium) moieties at positions 2 and 6 of the 1,4-DHP ring. Diludine and DHPs of group 3 exerted antiradical activities, unlike compounds of group 2. However, novel DHPs had cell type and concentration dependent effects on (3)H-thymidine incorporation, while diludine did not. Hence, IB-32 (group 2) suppressed the growth of HOS and HeLa, enhancing growth of L929 cells, while K-2-11 (group 3) enhanced growth of every cell line tested, even in the presence of doxorubicin. Therefore, growth regulating and antiradical activity principles of novel DHPs should be further studied to find if DHPs of group 2 could selectively suppress cancer growth and if those of group 3 promote wound healing. Hindawi 2017 2017-04-03 /pmc/articles/PMC5394904/ /pubmed/28473879 http://dx.doi.org/10.1155/2017/4069839 Text en Copyright © 2017 Imanta Bruvere et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bruvere, Imanta
Bisenieks, Egils
Poikans, Janis
Uldrikis, Janis
Plotniece, Aiva
Pajuste, Karlis
Rucins, Martins
Vigante, Brigita
Kalme, Zenta
Gosteva, Marina
Domracheva, Ilona
Velena, Astrida
Vukovic, Tea
Milkovic, Lidija
Duburs, Gunars
Zarkovic, Neven
Dihydropyridine Derivatives as Cell Growth Modulators In Vitro
title Dihydropyridine Derivatives as Cell Growth Modulators In Vitro
title_full Dihydropyridine Derivatives as Cell Growth Modulators In Vitro
title_fullStr Dihydropyridine Derivatives as Cell Growth Modulators In Vitro
title_full_unstemmed Dihydropyridine Derivatives as Cell Growth Modulators In Vitro
title_short Dihydropyridine Derivatives as Cell Growth Modulators In Vitro
title_sort dihydropyridine derivatives as cell growth modulators in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394904/
https://www.ncbi.nlm.nih.gov/pubmed/28473879
http://dx.doi.org/10.1155/2017/4069839
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