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. 2004 Oct 15;10(20):3048-52.
doi: 10.3748/wjg.v10.i20.3048.

"VSports注册入口" Effect of resveratrol and in combination with 5-FU on murine liver cancer

Affiliations

Effect of resveratrol and in combination with 5-FU on murine liver cancer

Sheng-Li Wu et al. World J Gastroenterol. .

Abstract

Aim: To study the anti-tumor effect of resveratrol and in combination with 5-FU on murine liver cancer VSports手机版. .

Methods: Transplantable murine hepatoma22 model was used to evaluate the anti-tumor activity of resveratrol (RES) alone or in combination with 5-FU in vivo. H22 cell cycles were analyzed with flow cytometry V体育安卓版. .

Results: Resveratrol could inhibit the growth of murine hepatoma22, after the mice bearing H22 tumor were treated with 10 mg/kg or 15 mg/kg resveratrol for ten days, and the inhibition rates were 36. 3% (n = 10) and 49. 3% (n = 9), respectively, which increased obviously compared with that in control group (85+/-22 vs 68+/-17, P<0 V体育ios版. 01). RES could induce the S phase arrest of H22 cells, and increase the percentage of cells in S phase from 59. 1% (n = 9) to 73. 5% (n = 9) in a dose-dependent manner (P<0. 05). The enhanced inhibition of tumor growth by 5-FU was also observed in hepatoma22 bearing mice when 5-FU was administered in combination with 10 mg/kg resveratrol. The inhibition rates for 20 mg/kg or 10 mg/kg 5-FU in combination with 10 mg/kg resveratrol were 77. 4% and 72. 4%, respectively, compared with the group of 20 mg/kg or 10 mg/kg 5-FU alone, in which the inhibition rates were 53. 4% and 43. 8%, respectively (n = 8). There was a statistical significance between the combination group and 5-FU group. .

Conclusion: RES could induce the S phase arrest of H22 cells and enhance the anti-tumor effect of 5-FU on murine hepatoma22 and antagonize its toxicity markedly VSports最新版本. These results suggest that resveratrol, as a biochemical modulator to enhance the therapeutic effects of 5-FU, may be potentially useful in cancer chemotherapy. .

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Figures

Figure 1
Figure 1
Number of H22 cell cycles in transplanted liver can-cer of mouse treated with RPMI-1640 (A) or 15.0 mg/kg (B).
Figure 2
Figure 2
Tumor size of mice treated with 10.0 mg/kg RES + 20.0 mg/kg 5-FU (tumor A: 3.5 × 3.1 × 2.6 mm) and RPMI-1640 (tumor B: 4.8 × 4.7 × 4.2 mm; tumor C: 5.3 × 5.2 × 4.8 mm).
Figure 3
Figure 3
Morphologic observation of tumor tissues of mice treated with RPMI-1640 (A) or 10.0 mg/kg RES + 20.0 mg/kg 5-FU(B).
Figure 4
Figure 4
Kaplan-meier curves of survival rates of tumor bearing mice when administered RPMI-1640, 10 mg/kg RES, 20 mg/kg 5-FU, and 5-FU (20.0 mg/kg) + RES (10.0 mg/kg).

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