The effects of 18F-FDG on the proliferation of HepG2 liver cancer cells
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The effects of 18F-FDG on the proliferation of HepG2 liver cancer cells
Journal of Radiation Research and Radiation ProcessingVol. 28, Issue 6, Pages: 357-362(2010)
作者机构:
1.安徽医科大学核医学教研室 合肥 230032
2.安徽省立医院PET-CT中心 合肥 230001
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WANG Mingming, SI Yuan, QIU Jun, et al. The effects of 18F-FDG on the proliferation of HepG2 liver cancer cells. [J]. Journal of Radiation Research and Radiation Processing 28(6):357-362(2010)
DOI:
WANG Mingming, SI Yuan, QIU Jun, et al. The effects of 18F-FDG on the proliferation of HepG2 liver cancer cells. [J]. Journal of Radiation Research and Radiation Processing 28(6):357-362(2010)DOI:
The effects of 18F-FDG on the proliferation of HepG2 liver cancer cells
The influence of ,18,F-FDG on the proliferation of HepG2 liver cancer cell was investigated and related possible mechanism was elucidated in this paper. HepG2 liver cancer cells were conventionally cultured. The cells during the phase of logarithmic growth were divided into different groups of ,18,F-FDG treatment and control groups. At 6,12 and 24h after treatment of 0—92.5×10,6,Bq/mL of ,18,F-FDG, inverted microscopy, the cell apoptosis was analyzed by use of flow cytometry and reverse transcription-polymerase chain reaction to analyze meanwhile the content of reactive oxygen species (ROS) and expression of p53 gene in cells induced by ,18,F-FDG, were determined respectively. After exposure to ,18,F-FDG, the apoptotic morphological changes of HepG2 liver cancer cells were observed. It was found that inhibition rate of cell proliferation, production of ROS and apoptosis rate increased with the radioactivity concentration of ,18,F-FDG in the range of 0—92.5×10,6,Bq/mLwhile the expression of p53 gene increased gradually. The results indicate that ,18,F-FDG may inhibit the proliferation of HepG2 liver cancer cells by apoptosis and increment of inhibition rate.
关键词
18氟-氟代脱氧葡萄糖HepG2肝癌细胞细胞增殖细胞凋亡
Keywords
18F-2-Deoxy-2-Fluoro-D-Glucose (18F-FDG)HepG2 liver cancer cellCells proliferationApoptosis