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Effects of karanjin on cell cycle arrest and apoptosis in human A549, HepG2 and HL-60 cancer cells
Guo, Jian-Ru; Chen, Qian-Qian; Lam, Christopher Wai-Kei; Zhang, Wei.
Afiliação
  • Guo, Jian-Ru; Macau University of Science and Technology. Macau Institute for Applied Research in Medicine and Health. State Key Laboratory of Quality Research in Chinese Medicines. Macau. CN
  • Chen, Qian-Qian; Macau University of Science and Technology. Macau Institute for Applied Research in Medicine and Health. State Key Laboratory of Quality Research in Chinese Medicines. Macau. CN
  • Lam, Christopher Wai-Kei; Macau University of Science and Technology. Macau Institute for Applied Research in Medicine and Health. State Key Laboratory of Quality Research in Chinese Medicines. Macau. CN
  • Zhang, Wei; Macau University of Science and Technology. Macau Institute for Applied Research in Medicine and Health. State Key Laboratory of Quality Research in Chinese Medicines. Macau. CN
Biol. Res ; 48: 1-7, 2015. ilus, graf, tab
Article em En | LILACS | ID: biblio-950804
Biblioteca responsável: CL1.1
ABSTRACT

BACKGROUND:

We have investigated the potential anticancer effects of karanjin, a principal furanoflavonol constituent of the Chinese medicine Fordia cauliflora, using cytotoxic assay, cell cycle arrest, and induction of apoptosis in three human cancer cell lines (A549, HepG2 and HL-60 cells).

RESULTS:

MTT cytotoxic assay showed that karanjin could inhibit the proliferation and viability of all three cancer cells. The induction of cell cycle arrest was observed via a PI (propidium iodide)/RNase Staining Buffer detection kit and analyzed by flow cytometry karanjin could dose-dependently induce cell cycle arrest at G2/M phase in the three cell lines. Cell apoptosis was assessed by Annexin V-FITC/PI staining all three cancer cells treated with karanjin exhibited significantly increased apoptotic rates, especially in the percentage of late apoptosis cells.

CONCLUSION:

Karanjin can induce cancer cell death through cell cycle arrest and enhance apoptosis. This compound may be effective clinically for cancer pharmacotherapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Assunto principal: Benzopiranos / Extratos Vegetais / Apoptose / Proliferação de Células / Pontos de Checagem do Ciclo Celular / Fabaceae / Antineoplásicos Fitogênicos Limite: Humans Idioma: En Revista: Biol. Res Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Assunto principal: Benzopiranos / Extratos Vegetais / Apoptose / Proliferação de Células / Pontos de Checagem do Ciclo Celular / Fabaceae / Antineoplásicos Fitogênicos Limite: Humans Idioma: En Revista: Biol. Res Ano de publicação: 2015 Tipo de documento: Article