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扶正抑瘤颗粒通过调节免疫功能和诱导细胞凋亡在体内和体外抑制肝癌的生长。

Fuzheng Yiliu Granule inhibits the growth of hepatocellular cancer by regulating immune function and inducing apoptosis in vivo and in vitro.

机构信息

Academy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, China.

出版信息

Chin J Integr Med. 2011 Sep;17(9):691-7. doi: 10.1007/s11655-011-0847-3. Epub 2011 Sep 11.

DOI:10.1007/s11655-011-0847-3
PMID:21910071
Abstract

OBJECTIVE

To study the inhibitory effect of Fuzheng Yiliu Granule (FYG) on hepatocellular cancer (HCC) and investigate the mechanism mediating its bioactivity.

METHODS

H22 tumor-bearing ICR mice were treated with FYG [3.6 g/(kg·d)] for 5 days. Tumor volume and tumor weight, percentages of CD3(+), CD4(+), CD8(+), and natural killer (NK) cells in peripheral blood, tumor apoptosis and serum levels of interleukin-2 (IL-2), and tumor necrosis factor-α (TNF-α) were evaluated. FYG-containing serum was prepared from SD rats treated for 7 days [high dose 3.6 g/(kg·d); middle dose 1.8 g/(kg·d); low dose 0.9 g/(kg·d)]. Cell cycle, cell viability, and apoptosis were evaluated after HepG2 cell line was cultured in FYG-containing serum for 48 h. The levels of IL-2 and TNF-α in FYG-containing serum were also determined.

RESULTS

FYG produced a potent antitumor effect (P<0.01) and induced marked apoptosis of the tumor tissue (P<0.05). Mice treated with FYG had higher percentages of CD3(+) and CD4(+) (P<0.05), and more NK cells (P<0.01) in the peripheral blood than those in the animals treated with normal saline. Mice receiving FYG had the highest serum levels of IL-2 and TNF-α (P<0.01). High-dose FYG-containing serum significantly decreased HepG2 cell viability, inhibited cell proliferation (P<0.05), and induced apoptosis (P<0.01). In addition, the levels of IL-2 and TNF-α of high-dose-containing serum were higher than the blank serum (P<0.01).

CONCLUSION

FYG could inhibit HCC growth by regulating immune function and inducing apoptosis of tumor cells in vivo and in vitro.

摘要

目的

研究扶正抑瘤颗粒(FYG)对肝癌(HCC)的抑制作用,并探讨介导其生物活性的机制。

方法

用 FYG [3.6 g/(kg·d)] 处理荷瘤 ICR 小鼠 5 天。评估肿瘤体积和肿瘤重量、外周血中 CD3(+)、CD4(+)、CD8(+)和自然杀伤(NK)细胞的百分比、肿瘤凋亡以及血清中白细胞介素-2(IL-2)和肿瘤坏死因子-α(TNF-α)的水平。用 FYG 处理 SD 大鼠 7 天[高剂量 3.6 g/(kg·d);中剂量 1.8 g/(kg·d);低剂量 0.9 g/(kg·d)]制备 FYG 含药血清。用 FYG 含药血清培养 HepG2 细胞系 48 h 后,评估细胞周期、细胞活力和细胞凋亡。还测定 FYG 含药血清中 IL-2 和 TNF-α的水平。

结果

FYG 产生了强大的抗肿瘤作用(P<0.01),并诱导肿瘤组织明显凋亡(P<0.05)。与生理盐水处理的动物相比,用 FYG 处理的小鼠外周血中 CD3(+)和 CD4(+)的百分比更高(P<0.05),NK 细胞更多(P<0.01)。接受 FYG 的小鼠血清中 IL-2 和 TNF-α水平最高(P<0.01)。高剂量 FYG 含药血清显著降低 HepG2 细胞活力,抑制细胞增殖(P<0.05),并诱导细胞凋亡(P<0.01)。此外,高剂量含药血清中 IL-2 和 TNF-α的水平高于空白血清(P<0.01)。

结论

FYG 可通过调节免疫功能和诱导体内、体外肿瘤细胞凋亡来抑制 HCC 生长。

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