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Dynamic influence of Rhein lysinate on HeLa cells

  • Authors:
    • Jiang Liu
    • Yong-Zhan Zhen
    • Ju Cui
    • Gang Hu
    • Jie Wei
    • Rong Xu
    • Ping Tu
    • Ya-Jun Lin
  • View Affiliations / Copyright

    Affiliations: The MOH Key Laboratory of Geriatrics, Beijing Hospital, National Center of Gerontology, Beijing 100730, P.R. China, Hebei Key Laboratory for Chronic Diseases, Tangshan Key Laboratory for Preclinical and Basic Research on Chronic Diseases, School of Basic Medical Sciences, North China University of Science and Technology, Tangshan, Hebei 063000, P.R. China, Department of Endocrinology, The Third Hospital of Nanchang City, Nanchang, Jiangxi 330009, P.R. China
    Copyright: © Liu et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 2047-2055
    |
    Published online on: September 5, 2018
       https://doi.org/10.3892/ijo.2018.4554
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Abstract

In a previous study, it was demonstrated that Rhein lysinate (RHL) inhibited HeLa cell proliferation via a specific mechanism. The aim of the present study was to clarify the mechanism of RHL by investigating its effect on mitochondrial damage and cell apoptosis. The results indicated that RHL inhibited cell growth and proliferation in HeLa cells. HeLa cells treated with RHL developed extensive vacuolization in a dose- and time-dependent manner. Ultrastructure analysis using transmission electron microscopy revealed that the vacuoles observed were damaged mitochondria and endoplasmic reticulum. The effects of RHL on mitochondria were further confirmed by a decrease in mitochondrial membrane potential and increased generation of reactive oxygen species. The mitochondrial proteome was analyzed, and the results demonstrated that the expression of the cytoskeletal protein keratin and dermal papilla derived protein 12 (associated with the oxidation-reduction process), which are associated with mitochondrial structure and function, were decreased compared with the untreated control group. Hoechst staining, flow cytometry and western blotting also revealed that apoptosis was induced at 24 h following RHL treatment. These results confirm that RHL toxicity in HeLa cells is a dynamic process. Vacuolar degeneration appeared in HeLa cells treated with 160 µmol/l RHL during the first 6 h and with the extension of RHL treatment, cell apoptosis was presented at ~24 h in HeLa cells.
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Copy and paste a formatted citation
Spandidos Publications style
Liu J, Zhen Y, Cui J, Hu G, Wei J, Xu R, Tu P and Lin Y: Dynamic influence of Rhein lysinate on HeLa cells. Int J Oncol 53: 2047-2055, 2018.
APA
Liu, J., Zhen, Y., Cui, J., Hu, G., Wei, J., Xu, R. ... Lin, Y. (2018). Dynamic influence of Rhein lysinate on HeLa cells. International Journal of Oncology, 53, 2047-2055. https://doi.org/10.3892/ijo.2018.4554
MLA
Liu, J., Zhen, Y., Cui, J., Hu, G., Wei, J., Xu, R., Tu, P., Lin, Y."Dynamic influence of Rhein lysinate on HeLa cells". International Journal of Oncology 53.5 (2018): 2047-2055.
Chicago
Liu, J., Zhen, Y., Cui, J., Hu, G., Wei, J., Xu, R., Tu, P., Lin, Y."Dynamic influence of Rhein lysinate on HeLa cells". International Journal of Oncology 53, no. 5 (2018): 2047-2055. https://doi.org/10.3892/ijo.2018.4554
Copy and paste a formatted citation
x
Spandidos Publications style
Liu J, Zhen Y, Cui J, Hu G, Wei J, Xu R, Tu P and Lin Y: Dynamic influence of Rhein lysinate on HeLa cells. Int J Oncol 53: 2047-2055, 2018.
APA
Liu, J., Zhen, Y., Cui, J., Hu, G., Wei, J., Xu, R. ... Lin, Y. (2018). Dynamic influence of Rhein lysinate on HeLa cells. International Journal of Oncology, 53, 2047-2055. https://doi.org/10.3892/ijo.2018.4554
MLA
Liu, J., Zhen, Y., Cui, J., Hu, G., Wei, J., Xu, R., Tu, P., Lin, Y."Dynamic influence of Rhein lysinate on HeLa cells". International Journal of Oncology 53.5 (2018): 2047-2055.
Chicago
Liu, J., Zhen, Y., Cui, J., Hu, G., Wei, J., Xu, R., Tu, P., Lin, Y."Dynamic influence of Rhein lysinate on HeLa cells". International Journal of Oncology 53, no. 5 (2018): 2047-2055. https://doi.org/10.3892/ijo.2018.4554
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