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Screening of cytotoxic or cytostatic flavonoids with quantitative Fluorescent Ubiquitination-based Cell Cycle Indicator-based cell cycle assay.
Go, Young-Hyun; Lee, Hyo-Ju; Kong, Hyeon-Joon; Jeong, Ho-Chang; Lee, Dong Young; Hong, Soon-Ki; Sung, Sang Hyun; Kwon, Ok-Seon; Cha, Hyuk-Jin.
Affiliation
  • Go YH; College of Natural Sciences, Department of Life Sciences, Sogang University, Seoul, Republic of Korea.
  • Lee HJ; College of Natural Sciences, Department of Life Sciences, Sogang University, Seoul, Republic of Korea.
  • Kong HJ; College of Natural Sciences, Department of Life Sciences, Sogang University, Seoul, Republic of Korea.
  • Jeong HC; College of Natural Sciences, Department of Life Sciences, Sogang University, Seoul, Republic of Korea.
  • Lee DY; College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.
  • Hong SK; College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.
  • Sung SH; College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.
  • Kwon OS; College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.
  • Cha HJ; College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.
R Soc Open Sci ; 5(12): 181303, 2018 Dec.
Article de En | MEDLINE | ID: mdl-30662739
ABSTRACT
The Fluorescent Ubiquitination-based Cell Cycle Indicator (FUCCI) system can be used not only to study gene expression at a specific cell cycle stage, but also to monitor cell cycle transitions in real time. In this study, we used a single clone of FUCCI-expressing HeLa cells (FUCCI-HeLa cells) and monitored the cell cycle in individual live cells over time by determining the ratios between red fluorescence (RF) of RFP-Cdt1 and green fluorescence (GF) of GFP-Geminin. Cytotoxic and cytostatic compounds, the latter of which induced G2 or mitotic arrest, were identified based on periodic cycling of the RF/GF and GF/RF ratios in FUCCI-HeLa cells treated with anti-cancer drugs. With this cell cycle monitoring system, ten flavonoids were screened. Of these, apigenin and luteolin, which have a flavone backbone, were cytotoxic, whereas kaempferol, which has a flavonol backbone, was cytostatic and induced G2 arrest. In summary, we developed a system to quantitatively monitor the cell cycle in real time. This system can be used to identify novel compounds that modulate the cell cycle and to investigate structure-activity relationships.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Diagnostic_studies / Screening_studies Langue: En Journal: R Soc Open Sci Année: 2018 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Diagnostic_studies / Screening_studies Langue: En Journal: R Soc Open Sci Année: 2018 Type de document: Article