Fuzheng Yiliu Granule (扶正抑瘤颗粒) inhibits the growth of hepatocellular cancer by regulating immune function and inducing apoptosis in vivo and in vitro
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Fuzheng Yiliu Granule (扶正抑瘤颗粒) inhibits the growth of hepatocellular cancer by regulating immune function and inducing apoptosis in vivo and in vitro
Fuzheng Yiliu Granule (扶正抑瘤颗粒) inhibits the growth of hepatocellular cancer by regulating immune function and inducing apoptosis in vivo and in vitro
中国结合医学杂志(英文版)2011年17卷第9期 页码:691-697
Affiliations:
Academy of Integrative Medicine, Fujian University of Traditional Chinese Medicine,Fuzhou,China
Author bio:
Funds:
Supported by CHEN Ke-ji Integrative Medicine Development Fund (No. CKJ2010020);International Science Joint Project of the Ministry of Science and Technology of the People's Republic of China (No. 2008DFA32200);Project of Department of Education of Fujian Province (No. JA09136)
Cao, Zy., Chen, Xz., Liao, Lm. et al. Fuzheng Yiliu Granule (扶正抑瘤颗粒) inhibits the growth of hepatocellular cancer by regulating immune function and inducing apoptosis in vivo and in vitro, ., Chin. J. Integr. Med. 17, 691 (2011). https://doi.org/10.1007/s11655-011-0847-3
Zhi-yun Cao, Xu-zheng Chen, Lian-ming Liao, et al. Fuzheng Yiliu Granule (扶正抑瘤颗粒) inhibits the growth of hepatocellular cancer by regulating immune function and inducing apoptosis in vivo and in vitro[J]. Chinese Journal of Integrative Medicine, 2011,17(9):691-697.
Cao, Zy., Chen, Xz., Liao, Lm. et al. Fuzheng Yiliu Granule (扶正抑瘤颗粒) inhibits the growth of hepatocellular cancer by regulating immune function and inducing apoptosis in vivo and in vitro, ., Chin. J. Integr. Med. 17, 691 (2011). https://doi.org/10.1007/s11655-011-0847-3DOI:
Zhi-yun Cao, Xu-zheng Chen, Lian-ming Liao, et al. Fuzheng Yiliu Granule (扶正抑瘤颗粒) inhibits the growth of hepatocellular cancer by regulating immune function and inducing apoptosis in vivo and in vitro[J]. Chinese Journal of Integrative Medicine, 2011,17(9):691-697. DOI: 10.1007/s11655-011-0847-3.
Fuzheng Yiliu Granule (扶正抑瘤颗粒) inhibits the growth of hepatocellular cancer by regulating immune function and inducing apoptosis in vivo and in vitro
摘要
To study the inhibitory effect of Fuzheng Yiliu Granule (扶正抑瘤颗粒
FYG) on hepatocellular cancer (HCC) and investigate the mechanism mediating its bioactivity. 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. 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). FYG could inhibit HCC growth by regulating immune function and inducing apoptosis of tumor cells in vivo and in vitro.
Abstract
To study the inhibitory effect of Fuzheng Yiliu Granule (扶正抑瘤颗粒
FYG) on hepatocellular cancer (HCC) and investigate the mechanism mediating its bioactivity. 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. 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). FYG could inhibit HCC growth by regulating immune function and inducing apoptosis of tumor cells in vivo and in vitro.
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Department of Biochemistry, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran
Department of Immunology, School of Medical Sciences, Tarbiat Modares University, Tehran
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Department of Nursing, Min-Hwei College of Health Care Management, Tainan
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