| 論文名 |
[Effects end mechanisms of curcumol beta-cyclodextrin compound on the proliferation and apoptosls of esophageal carcinoma cell line TE-1]. |
| 著者 |
Zhao Jing
Cong-Ying Xie
Zhi-Qin Wu
Fang Xu
Chang-Lin Zou
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| キーワード |
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| 出版年月 |
1970年1月 |
| 発表先 |
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2013 Jan;33(1):85-9. |
| WEBサイト |
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| 論文概要（和文） |
[クルクモールベータシクロデキストリン化合物の増殖と食道癌細胞株TE-1のアポトーシスに対するエンドメカニズムに影響]。 |
| 論文概要（英文） |
Objective: To investigate the effects and mechanisms of Curcumol beta-cyclodextrin Compound (CbetaC) on the proliferation and apoptosis of esophageal carcinoma cell line TE-1. Methods: The CbetaC was prepared by saturated solution and confirmed by infrared absorption spectroscopy. The effects of CbetaC (at 25, 50, 100 mg/L) on the proliferation of human esophageal carcinoma cell line TE-1 in vitro was analyzed by MTT assay. The cell cycles and apoptosis were detected by flow cytometer. The relative expression of survivin mRNA was detected by real-time fluorescent quantitative PCR and calculated by the 2(-deltaCt) method. The protein expression of survivin was measured by Western blot. Results: Compared with the control group, results of MTT showed that CbetaC at each dose significantly inhibited the proliferation of TE-1 cells in a dose-dependent manner (P < 0.05). The results of flow cytometry showed that CbetaC resulted in the cell cycle arrest at G0/G1 and G2/M phase, and promoted the cell apoptosis. Besides, when compared with the control group, the protein and mRNA expressions of survivin obviously decreased in each CbetaC group (P < 0.05). Conclusions: CbetaC could inhibit the proliferation of esophageal carcinoma cell TE-1 and promote the apoptosis. Its inhibition on the survivin expression was correlated with its inhibition on the malignant phenotypes of esophageal carcinoma cells. |
