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Effects of ginsenoside Rh2(GS-Rh2) on cell cycle of Eca-109 esophageal carcinoma cell line / 中国中药杂志
China Journal of Chinese Materia Medica ; (24): 1617-1621, 2005.
Article in Chinese | WPRIM | ID: wpr-287324
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the effects of ginsenoside Rh2 (GS-Rh2) on growth inhibition and cell cycle of Eca-109 esophageal carcinoma cell line in culture.</p><p><b>METHOD</b>The effects of GS-Rh2 on cell growth inhibition was detected by MTT assay. Cell cycle was analyzed by flow cytometry (FCM). Cell morphology was observed by a light microscope after HE staining. The protein expression of cell cycle components (cyclinE, CDK2, p21WAF1) were examined by immunocytochemistry and Western blot. The mRNA expression were examined by semiquantitative RT-PCR.</p><p><b>RESULT</b>GS-Rh2 inhibited the proliferation of Eca-109 cells in dose and time-dependent manners. The inhibition rate was about 50% after 1-day treatment with 20 microg x mL(-1) GS-Rh2 x 20 microg x mL(-1) GS-Rh2 induced the mature differentiation and morphological reversion. With increasing dose of GS-Rh2 treatment, the cell number of G0/G1 phase was increased, whereas it decreased at S and G2/M phase. There was significant difference between 10, 20 microg x mL(-1) GS-Rh2 groups and the corresponding group without GS-Rh2 treatement. After treating cells by 20 microg x mL(-1) GS-Rh2 for 1, 2, 3 days individually, the protein and mRNA expression of both cyclinE and CDK2 reduced, while the expression of p21WAF1 enhanced gradually.</p><p><b>CONCLUSION</b>GS-Rh2 could arrest Eca-109 cells at G0/G1 phase and induce cell differentiation tending to normal. Furthermore, GS-Rh2 had an effect on expression of cell cycle components (cyclinE, CDK2 and p21WAF1) to inhibit Eca-109 cell proliferation.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Pharmacology / Plants, Medicinal / Time Factors / RNA, Messenger / Esophageal Neoplasms / Drugs, Chinese Herbal / Carcinoma, Squamous Cell / Cell Cycle / Chemistry Limits: Humans Language: Chinese Journal: China Journal of Chinese Materia Medica Year: 2005 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Pharmacology / Plants, Medicinal / Time Factors / RNA, Messenger / Esophageal Neoplasms / Drugs, Chinese Herbal / Carcinoma, Squamous Cell / Cell Cycle / Chemistry Limits: Humans Language: Chinese Journal: China Journal of Chinese Materia Medica Year: 2005 Type: Article