›› 2011, Vol. 23 ›› Issue (5): 374-376.doi: 10.3969/j.issn.1004-616x.2011.05.012
• 肿瘤防治 • Previous Articles Next Articles
LI Zhan-jun,LIN Fei,FAN Hui-hong,XU Kang-sen
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Abstract: OBJECTIVE: To observe the anticancer effect of the serum thymic factor(FTS) 9 peptide on human colon cancer HT-29 transplantation model in nude mice. METHODS: Nude mice were inoculated subcutaneously with human colon cancer HT-29 cells,grouping was performed when tumor reach a volume of approximately 100 mm3. Tumor-bearing nude mice were divided into 5 groups:FTS 9 peptide high,medium and low dose group (1.25, 0.625,0.312 mg/kg,respectively),positive control (cyclophosphamide,30 mg/kg) and blank control (saline),10 mice in each group. Mice were treated subcutaneously once a day for 28 days. Body weight,length and width of tumor were measured twice a week. Mice were sacrificed 24 h after the last treatment,body weight,length,width,volume and weight of tumor were measured,the relative tumor proliferation and inhibition rates were calculated. Experiment was repeated 3 times. RESULTS:Relative tumor volumes of FTS 9 peptide groups were significantly reduced compared with blank control (P<0.01 or P<0.05),relative tumor proliferation rates of FTS 9 peptide high,medium and low dose groups were 50%± 20%,62%±20% and 77% ± 35%, respectively. Tumor weights of FTS 9 peptide groups were significantly reduced compared with blank control (P<0.01), inhibition rate of FTS 9 peptide high,medium and low doses group were 45% ± 3%,35% ± 1% and 27 %±3%, respectively. Body weights of nude mice in each group were not significantly different (compared with blank control,P>0.05). CONCLUSION:The results showed that the FTS 9 peptide had an obvious inhibitory effect on transplanted tumor of human colon cancer HT-29.
Key words: anticancer effect, serum thymic factor 9 peptide, human colon cancer HT-29, nude mice test
LI Zhan-jun,LIN Fei,FAN Hui-hong,XU Kang-sen. The anticancer effect of serum thymic factor 9 peptide on human colon cancer HT-29[J]. , 2011, 23(5): 374-376.
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