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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.
Affiliation
  • Bruvere I; Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia.
  • Bisenieks E; Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia.
  • Poikans J; Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia.
  • Uldrikis J; Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia.
  • Plotniece A; Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia.
  • Pajuste K; Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia.
  • Rucins M; Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia.
  • Vigante B; Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia.
  • Kalme Z; Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia.
  • Gosteva M; Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia.
  • Domracheva I; Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia.
  • Velena A; Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia.
  • Vukovic T; Laboratory for Oxidative Stress, Rudjer Boskovic Institute, Bijenicka 54, 10000 Zagreb, Croatia.
  • Milkovic L; Laboratory for Oxidative Stress, Rudjer Boskovic Institute, Bijenicka 54, 10000 Zagreb, Croatia.
  • Duburs G; Latvian Institute of Organic Synthesis, 21 Aizkraukles Str., Riga LV-1006, Latvia.
  • Zarkovic N; Laboratory for Oxidative Stress, Rudjer Boskovic Institute, Bijenicka 54, 10000 Zagreb, Croatia.
Oxid Med Cell Longev ; 2017: 4069839, 2017.
Article in En | MEDLINE | ID: mdl-28473879
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 on 3H-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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Wound Healing / Dihydropyridines / Doxorubicin / Free Radical Scavengers / Neoplasms Limits: Animals / Humans Language: En Journal: Oxid Med Cell Longev Journal subject: METABOLISMO Year: 2017 Document type: Article Affiliation country: Latvia Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Wound Healing / Dihydropyridines / Doxorubicin / Free Radical Scavengers / Neoplasms Limits: Animals / Humans Language: En Journal: Oxid Med Cell Longev Journal subject: METABOLISMO Year: 2017 Document type: Article Affiliation country: Latvia Country of publication: United States