Dihydropyridine Derivatives as Cell Growth Modulators In Vitro

Author:

Bruvere Imanta1,Bisenieks Egils1,Poikans Janis1ORCID,Uldrikis Janis1,Plotniece Aiva1,Pajuste Karlis1,Rucins Martins1,Vigante Brigita1,Kalme Zenta1,Gosteva Marina1,Domracheva Ilona1,Velena Astrida1ORCID,Vukovic Tea2,Milkovic Lidija2,Duburs Gunars1ORCID,Zarkovic Neven2ORCID

Affiliation:

1. Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia

2. Laboratory for Oxidative Stress, Rudjer Boskovic Institute, Bijenicka 54, 10000 Zagreb, Croatia

Abstract

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 (3H-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 on3H-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.

Funder

Latvijas Zinatnes Padome

Publisher

Hindawi Limited

Subject

Cell Biology,Aging,General Medicine,Biochemistry

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