Inhibitory effect of extract of fungi of Huaier on hepatocellular carcinoma cells

Jianzhuang Ren, Chuansheng Zheng, Gansheng Feng, Huimin Liang, Xiangwen Xia, Jianlin Fang, Xuhua Duan, Hui Zhao

Current Medical Science ›› 2009, Vol. 29 ›› Issue (2) : 198-201.

Current Medical Science ›› 2009, Vol. 29 ›› Issue (2) : 198-201. DOI: 10.1007/s11596-009-0212-3
Article

Inhibitory effect of extract of fungi of Huaier on hepatocellular carcinoma cells

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Abstract

This study investigated the inhibitory effect of the extract of fungi of Huaier (EFH) on the growth of hepatocellular carcinoma (HCC) cells. Hep-G2 cells, a human HCC cell line, were cultured in DMEM containing 10% fetal bovine serum and treated with EFH of different concentrations (1, 2, 4, 8 mg/mL) for 24, 48 and 72 h respectively. The apoptosis rate of the cells was flow cytometrically measured. Thirty-six tumor-bearing New Zealand rabbits were randomly divided into 3 groups: group A (control group), in which the rabbits were infused with 0.2 mL/kg normal saline via the hepatic artery; group B (transhepatic artery chemoembolization [TACE] group), in which the rabbits were given lipiodol at 0.2 mL/kg plus MMC at 0.5 mg/kg via the hepatic artery; group C (TACE + EFH group ), in which EFH (500 mg/kg) were orally administered after TACE. Two weeks after TACE, the rabbits were sacrificed and the implanted tumors were sampled. The tumor volume and the necrosis rate were determined. The tumor tissues were immunohistochemically detected for the expressions of factor VIII, VEGF, P53, Bax and Bcl-2. The microvessel density (MVD) was calculated by counting the factor VIII-positive endothelial cells. Our results showed that after treatment with EFH, the apoptosis rate of Hep-G2 cells was enhanced in a concentration- and time-dependent manner. Two weeks after the treatment, the average tumor volume, the necrosis rate and the growth rate of the implanted tumor in group C were significantly different from those in groups A and B (P<0.05). MVD and VEGF expressions were significantly decreased in the group C when compared with those in groups B (P<0.05 for all). The Bax expression was weakest in group A and strongest in group C. The expressions of P53 and Bcl-2 were minimal in group C and maximal in group A. There were significant differences in the expressions of P53, Bax and Bcl-2 among the 3 groups (P<0.05 for all) and there was significant difference between group B and group C (P<0.05). It was concluded that EFH could suppress not only the growth of HCC cells but also tumor angiogenesis and it can induce the apoptosis of HCC cells. EFH serves as an alternative for the treatment of HCC.

Keywords

extract of fungi of Huaier / hepatocarcinoma / chemoembolization / rabbit VX2 tumor / apoptosis

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Jianzhuang Ren, Chuansheng Zheng, Gansheng Feng, Huimin Liang, Xiangwen Xia, Jianlin Fang, Xuhua Duan, Hui Zhao. Inhibitory effect of extract of fungi of Huaier on hepatocellular carcinoma cells. Current Medical Science, 2009, 29(2): 198‒201 https://doi.org/10.1007/s11596-009-0212-3

References

[1]
O’suilleabhainC.B., PoonR.T., YongJ.L., et al. . Factors predictive of 5-year survival after transarterial chemoembolization for inoperable hepatocellular carcinoma. Br J Surg, 2003, 90(3): 325-331
CrossRef Google scholar
[2]
LiadoL., VirgiliJ., FiguerasJ., et al. . A prognostic index of the survival of patients with unresectable hepatocellular carcinoma after transcatheter arterial chemoembolization. Cancer, 2000, 88(1): 50-57
CrossRef Google scholar
[3]
GuanY.S., YuanL.. Interventional treatments for hepatocellular carcinoma. Hepatobiliary Pancreat Dis Int, 2006, 5(4): 495-500
[4]
KongJ., FengG.S., XuL. e. a1.. Experimental Methodology of Transhepatic Arterial Chemoembolization in Rabbits: A Comparative Study. J Clin Radiol (Chinese), 2003, 22(3): 244-247
[5]
ZhouC.K., LiangH.M., LiX., et al. . Establishment of rabbit model bearing VX2 liver tumor experimentation and discussion of the selective hepatic arterial catheterization. J Intervent Radiol (Chinese), 2006, 15(2): 101-104
[6]
ParkY. N., KimY. B., YangK. M., et al. . Increased expression of vascular endothelial growth factor and angiogenesis in the early stage of multistep hepatocarcinogenesis. Arch Pathol Lab Med, 2000, 124(7): 1061-1065
[7]
WeidnerN., SempleJ.P., WelchW.R., et al. . Tumor angiogenesis and metastasis-correlation in invasive breast carcinoma. N Engl J Med, 1991, 324(1): 1-8
[8]
XuG.L., JiaW.D., MaJ.L., et al. . Experimental study of extract of funji of huaier on angiogenesis in vitro. Chin Pharmacol Bull (Chinese), 2003, 19(12): 1410-1412
[9]
HuangT., KongQ.Z., LuH.D., et al. . Experimental study of extract of funji of huaier inducing apoptosis of the human adenocarcinoma of lung A549 cells. Chin J Tuberc Respir Dis (Chinese), 2001, 24(8): 487-488
[10]
GerlR., VauxD.L.. Apoptosis in the development and treatment of cancer. Carcinogenesis, 2005, 26(2): 263-270
CrossRef Google scholar
[11]
VauxD. L.. Early work on the function of Bcl-2, an interview with David Vaux. Cell Death Differ, 2004, 11(11): 528-532
[12]
TophkhaneC., YangS., BalesW., et al. . Bcl-2 overexpression sensitizes MCF-7 cells to genistein by multiple mechanisms. Int J Oncol, 2007, 31(4): 867-874
[13]
WeiM.C., ZongW.X., ChengE.H., et al. . Pro-apoptotic BAX and BAK: a requisite gateway to mitochondrial dysfunction and death. Science, 2001, 292(5517): 727-730
CrossRef Google scholar
[14]
CoryS., AdamsJ.M.. The Bcl-2 family: regulators of the cellular life-or-death switch. Nat Rev Cancer, 2002, 2(9): 647-656
CrossRef Google scholar
[15]
SoiniY., VirkajarviN., LehtoV.P., et al. . Hepatocellular carcinomas with a high proliferation index and a low degree of apoptosis and necrosis are associated with a shortened survival.. Br J Cancer, 1996, 73(9): 1025-1030
[16]
MarsdenV.S., O’ConnorL., O’ReillyL.A., et al. . Apoptosis initiated by Bcl-2-regulated caspase activation independently of the cytochrome c/Apaf-1/caspase-9 apoptosome. Nature, 2002, 419(6907): 634-637
CrossRef Google scholar
[17]
FerraraN., KerbelR.S.. Angiogenesis as a therapeutic target. Nature, 2005, 438(7070): 967-974
CrossRef Google scholar
[18]
DvorakH.F., BrownL.F., DetmarM., et al. . Vascular permeability factor/vascular endothelial growth factor, microvascular hyperpermeability, and angiogenesis. Am J Pathol, 1995, 146(5): 1029-1039
[19]
YancopoulosG.D., DavisS., GaleN.W., et al. . Vascular-specific growth factors and blood vessel formation. Nature, 2000, 407(6801): 242-248
CrossRef Google scholar
[20]
HasanJ., ByersR., JaysonG.C.. Intra-tumoural microvessel density in human solid tumours. Br J Cancer, 2002, 86(10): 1566-1577
CrossRef Google scholar
[21]
FoxC.H., WhalenG. F., SandersM.M., et al. . Angiogenesis in normal tissue adjacent to colon cancer. J Surg Oncol, 1998, 69(4): 230-223
CrossRef Google scholar

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