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Effects of astragali radix on the growth of different cancer cell lines
Jiang Lin1, Hui-Fang Dong, J J Oppenheim
1Deportment of Gastroenterology, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200021, China. lin_jiang@hotmail.com
Aim:
To investigate the inhibitory effect of a Chinese herb medicine Astragali radix (AR) on growth of different cancer cell line.
Methods:
To observe the in vitro effects of AR on tumor cell proliferation by trypan blue exclusion, MTS method and tritium thymidine incorporation assay. Apoptosis was detected by DNA ladder method.
Results:
The inhibition rates of AR on the cell respiration of AGS, KATOIII, HT29, MDA231, MEL7 and MEL14 were 68.25 %, 62.36 %, 22.8 %, 27.69 %, 2.85 % and 5.14 % respectively at the concentration of 100 ug/ml; it inhibited AGS DNA synthesis by 87.33 % at the concentration of 50 ug/ml. The inhibitory effect on AGS was time-and dose-dependent. AR did not induce apoptosis in AGS cells.
Conclusion:
AR specifically inhibits gastric cancer cells growth in vitro and the mechanism is mainly cytostatic but not cytotoxic or inducing apoptosis.
Insights
Astragali radix (AR) effectively inhibits gastric cancer cell growth in vitro. This herbal medicine
Area of Science:
- Oncology
- Pharmacology
- Traditional Chinese Medicine
Background:
- Cancer remains a leading cause of mortality worldwide.
- Exploring novel therapeutic agents from natural sources is crucial for cancer treatment.
- Astragali radix (AR) is a widely used herb in Traditional Chinese Medicine.
Purpose of the Study:
- To evaluate the in vitro anticancer effects of Astragali radix (AR).
- To investigate the impact of AR on the proliferation and apoptosis of various cancer cell lines.
- To determine the specific mechanisms underlying AR's anti-cancer activity.
Main Methods:
- In vitro assays including trypan blue exclusion, MTS assay, and tritium thymidine incorporation were employed.
- DNA ladder assay was utilized to detect apoptosis.
- Cellular respiration inhibition was measured at various concentrations of AR.
Main Results:
- AR demonstrated significant inhibition of cancer cell respiration, with notable effects on AGS (68.25%) and KATOIII (62.36%) cells at 100 ug/ml.
- AR markedly inhibited DNA synthesis in AGS cells by 87.33% at 50 ug/ml, showing time- and dose-dependent effects.
- AR did not induce apoptosis in AGS cells, suggesting a cytostatic rather than cytotoxic mechanism.
Conclusions:
- Astragali radix (AR) exhibits specific inhibitory effects on gastric cancer cell growth in vitro.
- The primary mechanism of AR's action appears to be cytostatic, arresting cell growth without inducing apoptosis.
- AR represents a potential therapeutic candidate for gastric cancer, warranting further investigation into its cytostatic properties.
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