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  2. Griffipavixanthone from Garcinia oblongifolia champ induces cell apoptosis in human non-small-cell lung cancer H520 cells in vitro

Griffipavixanthone from Garcinia oblongifolia champ induces cell apoptosis in human non-small-cell lung cancer H520 cells in vitro

  • Molecules. 2014 Jan 27;19(2):1422-31. doi: 10.3390/molecules19021422.
Jun-Min Shi 1 Hui-Juan Huang 2 Sheng-Xiang Qiu 3 Shi-Xiu Feng 4 Xu-E Li 5
Affiliations

Affiliations

  • 1 School of Life Sciences, South China Normal University, Guangzhou 510631, China. amonolith@126.com.
  • 2 School of Life Sciences, South China Normal University, Guangzhou 510631, China. hjhuang1980@163.com.
  • 3 South China Botanical Garden, Chinese Academy of Sciences, Guangzhou 510650, China. qiusxscbg@163.com.
  • 4 Laboratory of Southern Subtropical Plant Diversity, Shenzhen Fairy Lake Botanical Garden, Chinese Academy of Sciences, Shenzhen 518004, China. fengsx2008@sohu.com.
  • 5 School of Life Sciences, South China Normal University, Guangzhou 510631, China. lixuescnu@126.com.
Abstract

Griffipavixanthone (GPX) is a dimeric xanthone which was isolated in a systematic investigation of Garcinia oblongifolia Champ. In this study, we investigate the effect of GPX on cell proliferation and Apoptosis on human Non-small-cell lung Cancer (NSCLC) cells in vitro and determine the mechanisms of its action. GPX inhibited the growth of H520 cells in dose- and time-dependent manners, with IC50 values of 3.03 ± 0.21 μM at 48 h. The morphologic characteristics of Apoptosis and apoptotic bodies were observed by fluorescence microscope and transmission electron microscope. In addition, Annexin V/PI double staining assay revealed that cells in early stage of Apoptosis were significantly increased upon GPX treatment dose-dependently. Rh123 staining assay indicated that GPX reduced the mitochondrial membrane potential. DCFH-DA staining revealed that intracellular ROS increased with GPX treatment. Moreover, GPX cleaved and activated Caspase-3. In summary, this study showed that GPX inhibited H520 cell proliferation in dose- and time-dependent manner. Further mechanistic study indicated that GPX induced cell Apoptosis through mitochondrial apoptotic pathway accompanying with ROS production. Our results demonstrate the potential application of GPX as an anti-non-small cell lung Cancer agent.

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