This study investigated the effects of CpG ODN1826 plus
radiotherapy (RT) on
tumor growth and angiogenesis of subcutaneous
tumor in a rat model. Four treatment groups were tested in which rats were injected with 100 μL CpG ODN1826 (1 μg/μL) or 100 μL vehicle, with and without exposure to 8 Gy after 2 h. At 7 days after inoculation of
lung cancer cells, drugs were injected in the
tumor and radiation was administered over 5 days, after which the rate of
tumor inhibition was calculated. Expression of
VEGF-C in
tumor tissue was seen in 10, 50, 80, and 100% of
tumors in the CpG ODN1826 + RT, CpG ODN1826, vehicle + RT, and vehicle alone groups, respectively, while positive expression of NRP-1 was seen in 10, 40, 90, and 100% of
tumors. The decreases in expression of
VEGF-C mRNA in the CpG ODN1826 + RT and CpG ODN1826 groups compared with the NS + RT and NS groups were significant (P < 0.01), as were the decreases in NRP-1
mRNA in the CpG ODN1826 + RT group compared with the CpG ODN1826 group (P < 0.01). Thus, CpG ODN1826 can significantly inhibit
tumor growth in a rat model, the mechanism of which may be related to inhibition of the expression of
VEGF-C and NRP-1, which have an inhibitory effect on angiogenesis.