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Experiment of inhibitive effect of Artemether on colorectal cancer growth and angiogenesis in BALB/c mice

Qi-shui Zhu, Zhiping Wu, Chengwei Gao, Yong-gui Wu, Xicai Wang

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Abstract

4002 Purpose: To explore the inhibitive effect of Artemether on colorectal cancer growth and angiogenesis in tumor bearing BALB/c mice. Methods:Forty-eight (24 male and 24 female) BALB/c mice that were subcutaneously implanted with CT-26 colorectal cell (2×106) were divided into 6 groups; each group contained 8 mice. They were low dose group (33.3 mg/kg; oral); middle dose group (50 mg/kg; oral); high dose group (66.6 mg/kg; oral); middle dose plus ferralia (50 mg/kg+1.5 mg/kg; oral); positive control group DDP (5 mg/kg; ip) and blank control normal saline (oral). Microvascular density (MVD) was observed and countered under the microscopy by immunohistochemistry. Results: Inhibitive rates of Artemether by oral administration at low, middle, and high dosages were 42.3%, 51.4%, and 52.0%, respectively, and had significant difference inhibitive effects on colorectal cancer growth (P =0.007, P =0.006, P =0.024 respectively). Combination ferralia and Artemether synergenic the inhibitive effect on tumor bearing mice. MVD in different therapy groups was significantly lower than that in normal saline control group (P

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4002 Purpose: To explore the inhibitive effect of Artemether on colorectal cancer growth and angiogenesis in tumor bearing BALB/c mice. Methods:Forty-eight (24 male and 24 female) BALB/c mice that were subcutaneously implanted with CT-26 colorectal cell (2×106) were divided into 6 groups; each group contained 8 mice. They were low dose group (33.3 mg/kg; oral); middle dose group (50 mg/kg; oral); high dose group (66.6 mg/kg; oral); middle dose plus ferralia (50 mg/kg+1.5 mg/kg; oral); positive control group DDP (5 mg/kg; ip) and blank control normal saline (oral). Microvascular density (MVD) was observed and countered under the microscopy by immunohistochemistry. Results: Inhibitive rates of Artemether by oral administration at low, middle, and high dosages were 42.3%, 51.4%, and 52.0%, respectively, and had significant difference inhibitive effects on colorectal cancer growth (P =0.007, P =0.006, P =0.024 respectively). Combination ferralia and Artemether synergenic the inhibitive effect on tumor bearing mice. MVD in different therapy groups was significantly lower than that in normal saline control group (P

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Available abstract

4002 Purpose: To explore the inhibitive effect of Artemether on colorectal cancer growth and angiogenesis in tumor bearing BALB/c mice. Methods:Forty-eight (24 male and 24 female) BALB/c mice that were subcutaneously implanted with CT-26 colorectal cell (2×106) were divided into 6 groups; each group contained 8 mice. They were low dose group (33.3 mg/kg; oral); middle dose group (50 mg/kg; oral); high dose group (66.6 mg/kg; oral); middle dose plus ferralia (50 mg/kg+1.5 mg/kg; oral); positive control group DDP (5 mg/kg; ip) and blank control normal saline (oral). Microvascular density (MVD) was observed and countered under the microscopy by immunohistochemistry. Results: Inhibitive rates of Artemether by oral administration at low, middle, and high dosages were 42.3%, 51.4%, and 52.0%, respectively, and had significant difference inhibitive effects on colorectal cancer growth (P =0.007, P =0.006, P =0.024 respectively). Combination ferralia and Artemether synergenic the inhibitive effect on tumor bearing mice. MVD in different therapy groups was significantly lower than that in normal saline control group (P

Key concepts: Artemether, Dose, Medicine, Saline, Angiogenesis, BALB/c, Colorectal cancer, Oral administration

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