LI Jing, WANG Pei-pei, HUANG Song, et al. Inhibition Effect and Mechanism of Xiancidan on Lewis Lung Cancer in Mice[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(11): 208-212.
LI Jing, WANG Pei-pei, HUANG Song, et al. Inhibition Effect and Mechanism of Xiancidan on Lewis Lung Cancer in Mice[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(11): 208-212. DOI: 10.11653/syfj2013110208.
Objective: To investigate the inhibition effects of Xiancidan(XCD) on the lung-cancer cell in Lewis tumor-bearing mice and explore its mechanism. Method: C57BL/6 mice were taken as model
and divided into model group
cis-platinum group
high dose group XCD
middle dose group XCD
low dose group XCD
combination of XCD and control group 5 days later
All groups were administrated for 13 days
and the respective dosage was 0
2.0(ip)
0.648(ig)
0.324(ig)
0.162(ig)
0.162(ig)+2.0(ip).To observe the effect of XCD on inhibition of the lung cancer cell and immune regulation
AnnexinⅤ-FITC/PI method was applied to determine the apoptosis and cycle of transplanted cancer cells and Western blot method was used to observe the p53
Bcl-2 gene expression. Result: ①The inhibition rate in positive control group
high dose group
middle dose group
low dose groupof XCD
combination of XCD and control group were(63.02±3.21)%
(46.59±2.60)%
(42.48±2.77)%
(15.74±1.94)%
(64.56±1.62)%.②The pleen Index of high dose group XCD
middle dose group XCD and low dose group were significantly different from model group(P<0.01). ③The apoptosis rate of model group
control group
high dose group XCD
middle dose group XCD
low dose group XCD
the combination group of XCD and positive drug was 0.04%
30.40%
14.80%
17.98%
16.04%
20.34%
respectively.④Compared with model group
the percentage of G0/G1 cell in positive control group
high dose group XCD
middle dose group XCD and the combination groupm was significantly decreased. ⑤The p53 expression and Bcl-2 rate was significantly different from model group. Conclusion: The XCD effective parts can inhibit the growth of lewis tumor
which is related to its apoptosis-inducing and immune regulation effect.