Objective:To study the regulating effect of Shiquandabu mixture combined with cisplatin on the tumor growth in colon cancer-bearing mice.Methods: SPF C57BL/6 males mice were selected as the experimental animals, made ...Objective:To study the regulating effect of Shiquandabu mixture combined with cisplatin on the tumor growth in colon cancer-bearing mice.Methods: SPF C57BL/6 males mice were selected as the experimental animals, made into tumor-bearing models through subcutaneous injection of colon cancer cells and then randomly divided into model group (normal saline intervention), cisplatin intervention group (10 mg/kg cisplatin intervention) and combined intervention group (10 mg/kg cisplatin + 3.9 mL Shiquandabu mixture intervention). 5 d, 10 d and 15 d after intervention, the tumor tissue mass as well as the expression of proliferation-related molecules and invasion-related molecules was determined.Results:5 d, 10 d and 15 d after intervention, the tumor mass of cisplatin intervention group and combined intervention group were significantly lower than that of model group, and the tumor mass of combined intervention group was significantly lower than that of cisplatin group;TPX2, Rac1, cyclinD1, SLP-2, CHD1L, LSD1 and N-cadherin expression in tumor tissue of cisplatin intervention group and combined intervention group were significantly lower than those of model group while RNF181 and E-cadherin expression were significantly higher than those of model group;TPX2, Rac1, cyclinD1, SLP-2, CHD1L, LSD1 and N-cadherin expression in tumor tissue of combined intervention group were significantly lower than those of cisplatin intervention group while RNF181 and E-cadherin expression were significantly higher than those of cisplatin intervention group.Conclusion:Shiquandabu mixture combined with cisplatin can more effectively inhibit the tumor growth in colon cancer-bearing mice than cisplatin monotherapy.展开更多
文摘Objective:To study the regulating effect of Shiquandabu mixture combined with cisplatin on the tumor growth in colon cancer-bearing mice.Methods: SPF C57BL/6 males mice were selected as the experimental animals, made into tumor-bearing models through subcutaneous injection of colon cancer cells and then randomly divided into model group (normal saline intervention), cisplatin intervention group (10 mg/kg cisplatin intervention) and combined intervention group (10 mg/kg cisplatin + 3.9 mL Shiquandabu mixture intervention). 5 d, 10 d and 15 d after intervention, the tumor tissue mass as well as the expression of proliferation-related molecules and invasion-related molecules was determined.Results:5 d, 10 d and 15 d after intervention, the tumor mass of cisplatin intervention group and combined intervention group were significantly lower than that of model group, and the tumor mass of combined intervention group was significantly lower than that of cisplatin group;TPX2, Rac1, cyclinD1, SLP-2, CHD1L, LSD1 and N-cadherin expression in tumor tissue of cisplatin intervention group and combined intervention group were significantly lower than those of model group while RNF181 and E-cadherin expression were significantly higher than those of model group;TPX2, Rac1, cyclinD1, SLP-2, CHD1L, LSD1 and N-cadherin expression in tumor tissue of combined intervention group were significantly lower than those of cisplatin intervention group while RNF181 and E-cadherin expression were significantly higher than those of cisplatin intervention group.Conclusion:Shiquandabu mixture combined with cisplatin can more effectively inhibit the tumor growth in colon cancer-bearing mice than cisplatin monotherapy.