4.7 Article

Stimulation of ROS Generation by Extract of Warburgia ugandensis Leading to G0/G1 Cell Cycle Arrest and Antiproliferation in A549 Cells

期刊

ANTIOXIDANTS
卷 10, 期 10, 页码 -

出版社

MDPI
DOI: 10.3390/antiox10101559

关键词

Warburgia ugandensis; A549 cells; G(0)/G(1) phase arrest; ROS; DNA damage

资金

  1. national Natural Science Foundation of China [81673580]
  2. Youth Innovation Promotion Association of the Chinese Academy of Sciences [2020337]

向作者/读者索取更多资源

The study demonstrated that the extract of Warburgia ugandensis Sprague (WUD) exhibited significant anti-proliferative effects on A549 cells by increasing intracellular ROS levels and subsequently modulating cell proliferation and G(0)/G(1) cell cycle progression.
Warburgia ugandensis Sprague (WU) is a traditional medicinal plant used for the treatment of various diseases, including cancer, in Africa. This study aimed to evaluate the anti-non-small cell lung cancer (NSCLC) activities of WU against A549 cells and to reveal potential molecular mechanisms. The cytotoxicity of various WU extracts was evaluated with HeLa (cervical cancer), HepG2 (liver cancer), HT-29 (colorectal cancer), and A549 (non-small cell lung cancer) cells by means of Sulforhodamine B (SRB) assay. Therein, the dimethyl carbonate extract of WU (WUD) was tested with the most potent anti-proliferative activity against the four cancer cell lines, and its effects on cell viability, cell cycle progression, DNA damage, intracellular reactive oxygen species (ROS), and expression levels of G(0)/G(1)-related proteins in A549 cells were further examined. First, it was found that WUD inhibited the proliferation of A549 cells in a time- and dose-dependent manner. In addition, WUD induced G(0)/G(1) phase arrest and modulated the expression of G(0)/G(1) phase-associated proteins Cyclin D1, Cyclin E1, and P27 in A549 cells. Furthermore, WUD increased the protein abundance of P27 by inhibiting FOXO3A/SKP2 axis-mediated protein degradation and also significantly induced the gamma H2AX expression and intracellular ROS generation of A549 cells. It was also found that the inhibitory effect of WUD on the proliferation and G(0)/G(1) cell cycle progression of A549 cells could be attenuated by NAC, a ROS scavenger. On the other hand, phytochemical analysis of WUD with UPLC-QTOF-MS/MS indicated 10 sesquiterpenoid compounds. In conclusion, WUD exhibited remarkable anti-proliferative effects on A549 cells by improving the intracellular ROS level and by subsequently modulating the cell proliferation and G(0)/G(1) cell cycle progression of A549 cells. These findings proved the good therapeutic potential of WU for the treatment of NSCLC.

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