Effects of Ferrocenyl 4-(Imino)-1,4-Dihydro-quinolines on Xenopus laevis Prophase I - Arrested Oocytes: Survival and Hormonal-Induced M-Phase Entry
Autor: | Arlette Lescuyer-Rousseau, Caroline Molinaro, Katia Cailliau, Angel Markey, Guillaume Marchand, Matthieu Marin, Sylvain Pellegrini, Till Bousquet, Jean-François Bodart, Lydie Pelinski, Nathalie Wambang, Alain Martoriati |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
ferrocenyldihydroquinoline Xenopus Cyclin B 010501 environmental sciences 01 natural sciences Catalysis lcsh:Chemistry Inorganic Chemistry Dephosphorylation 03 medical and health sciences Histone H3 Xenopus laevis Western blot medicine Physical and Theoretical Chemistry oocyte lcsh:QH301-705.5 Molecular Biology Spectroscopy 0105 earth and related environmental sciences Cyclin-dependent kinase 1 biology medicine.diagnostic_test Chemistry Organic Chemistry General Medicine biology.organism_classification Oocyte Molecular biology 3. Good health Computer Science Applications 030104 developmental biology medicine.anatomical_structure cell death lcsh:Biology (General) lcsh:QD1-999 metaphase II spindle biology.protein Phosphorylation |
Zdroj: | International Journal of Molecular Sciences Volume 21 Issue 9 International Journal of Molecular Sciences, Vol 21, Iss 3049, p 3049 (2020) |
ISSN: | 1422-0067 |
DOI: | 10.3390/ijms21093049 |
Popis: | Xenopus oocytes were used as cellular and molecular sentinels to assess the effects of a new class of organometallic compounds called ferrocenyl dihydroquinolines that have been developed as potential anti-cancer agents. One ferrocenyl dihydroquinoline compound exerted deleterious effects on oocyte survival after 48 h of incubation at 100 M. Two ferrocenyl dihydroquinoline compounds had an inhibitory effect on the resumption of progesterone induced oocyte meiosis, compared to controls without ferrocenyl groups. In these inhibited oocytes, no MPF (Cdk1/cyclin B) activity was detected by western blot analysis as shown by the lack of phosphorylation of histone H3. The dephosphorylation of the inhibitory Y15 residue of Cdk1 occurred but cyclin B was degraded. Moreover, two apoptotic death markers, the active caspase 3 and the phosphorylated histone H2, were detected. Only 7-chloro-1-ferrocenylmethyl-4-(phenylylimino)-1,4-dihydroquinoline (8) did not show any toxicity and allowed the assembly of a histologically normal metaphase II meiotic spindle while inhibiting the proliferation of cancer cell lines with a low IC50, suggesting that this compound appears suitable as an antimitotic agent. |
Databáze: | OpenAIRE |
Externí odkaz: | |
Nepřihlášeným uživatelům se plný text nezobrazuje | K zobrazení výsledku je třeba se přihlásit. |