XIE Bin, XIE Xiong, YU Gong, et al. Effect of Qingzao Jiufei Tang on Expressions of Invasion and Metastasis-related Proteins NF-B, VEGF, VEGFR-1, MMP-9 in Colon Carcinoma[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(17): 110-114.
XIE Bin, XIE Xiong, YU Gong, et al. Effect of Qingzao Jiufei Tang on Expressions of Invasion and Metastasis-related Proteins NF-B, VEGF, VEGFR-1, MMP-9 in Colon Carcinoma[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(17): 110-114. DOI: 10.13422/j.cnki.syfjx.2017170110.
matrix metalloprotein-9 (MMP-9) expression in CT26 mice colon cancer cells. Method: A total of 50 male BALB/c mice were randomly divided into model group
chemotherapy group [50 mg · kg-1 · (2d)-1]
high
medium and low-dose groups (15.2
7.6
3.8 g · kg-1 · d-1)
with 10 mice in each group. The colon cancer model was established by right axillary injection with CT26 cells. Qingzao Jiufei Tang group was given the corresponding dose of drug two weeks before modeling
5-FU group [50 mg · kg-1 · (2 d)-1] and model group (same volume of saline) started injection after modeling. Two weeks later
all of the mice were put to death
and tumor tissues were collected and weighed. We detected the expressions of NF-κB
VEGF
VEGFR-1
MMP-9 by the Western blot method. Result: The tumor weights of the high-dose group and the medium-dose group were decreased
compared with model group (P<0.01). The tumor inhibition rates of the chemotherapy group and high
middle and low-dose groups were 83.90%
60.98%
44.39%
21.46%. Compared with model group
the protein expressions of NF-κB and VEGF were significantly reduced
with significant differences between them (P<0.05
P<0.01). Compared with model group
the protein expressions of VEGFR-1 and MMP-9 were significantly lower in high
medium and low-dose groups
with significant differences between them (P<0.05
P<0.01). Conclusion: Qingzao Jiufei Tang can reduce the protein expressions of NF-κB
VEGF
VEGFR-1
MMP-9
and inhibit the invasion and metastasis of colon cancer cells in CT26 mice.