Anti-angiogenic potential of Gleditsia sinensis fruit extract

被引:10
作者
Chow, LMC [1 ]
Chui, CH
Tang, JCO
Lau, FY
Yau, MYC
Cheng, GYM
Wong, RSM
Lai, PBS
Leung, TWT
Teo, ITN
Cheung, F
Guo, D
Chan, ASC
机构
[1] Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Hong Kong, Hong Kong, Peoples R China
[2] Hong Kong Polytech Univ, Inst Mol Technol Drug Discovery & Synth, Cent Lab, Hong Kong, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Hong Kong, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Surg, Hong Kong, Hong Kong, Peoples R China
[5] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Clin Oncol, Hong Kong, Hong Kong, Peoples R China
[6] Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100083, Peoples R China
关键词
antiangiogenesis; traditional Chinese medicine;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
Blood supply plays a crucial role in solid tumour development and leukaemogenesis. It has been suggested that blocking of angiogenesis could be possible in cancer therapy. We have demonstrated the antiproliferative activity of Gleditsia sinensis fruit extract (GSE) on various human solid tumour cancer cell lines as well as leukaemia cell lines and primary cultured leukaemia cells obtained from leukaemia patients. However, the antiangiogenic potential of GSE has not been demonstrated. Here we demonstrated that GSE could reduce vascular endothelial growth factor (VEGF) mRNA expression in dose- and time course-dependently in MDA-MB231 breast cancer and HepG2 hepatoblastoma cell lines as measured by reverse transcriptase polymerase chain reaction. Enzyme-linked immunosorbent assay further showed that GSE could reduce the VEGF secretion from various cancer cell lines including MDA-MB231, HepG2, HL-60 (acute promyelocytic leukaemia) and eleven primary cultured leukaemia cells obtained from acute myelogenous leukaemia patients. In vivo chick chorioallantoic membrane assay illustrated that GSE could reduce the angiogenic activity of basic fibroblast growth factor. Taken together, the information suggested that GSE could be potentially used as an angiogenic inhibitor in both solid tumour and leukaemia therapy.
引用
收藏
页码:269 / 273
页数:5
相关论文
共 21 条
[1]
[Anonymous], 1995, The molecular basis of cancer
[2]
Tie2 receptor ligands, angiopoietin-1 and angiopoietin-2, modulate VEGF-induced postnatal neovascularization [J].
Asahara, T ;
Chen, DH ;
Takahashi, T ;
Fujikawa, K ;
Kearney, M ;
Magner, M ;
Yancopoulos, GD ;
Isner, JM .
CIRCULATION RESEARCH, 1998, 83 (03) :233-240
[3]
Brown KJ, 1996, LAB INVEST, V75, P539
[4]
Antiproliferative activity of the extract of Gleditsia sinensis fruit on human solid tumour cell lines [J].
Chow, LMC ;
Tang, JCO ;
Teo, ITN ;
Chui, CH ;
Lau, FY ;
Leung, TWT ;
Cheng, G ;
Wong, RSM ;
Wong, ILK ;
Tsang, KMS ;
Tan, WQ ;
Zhao, YZ ;
Lai, KB ;
Lam, WH ;
Guo, DA ;
Chan, ASC .
CHEMOTHERAPY, 2002, 48 (06) :303-308
[5]
CHOW LMC, IN PRESS ONCOL REP
[6]
Increased bone marrow vascularization in patients with acute myeloid leukaemia: a possible role for vascular endothelial growth factor [J].
de Bont, ESJM ;
Rosati, S ;
Jacobs, S ;
Kamps, WA ;
Vellenga, E .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 113 (02) :296-304
[7]
Vascular endothelial growth factor, a possible paracrine growth factor in human acute myeloid leukemia [J].
Fiedler, W ;
Graeven, U ;
Ergun, S ;
Verago, S ;
Kilic, N ;
Stockschlader, M ;
Hossfeld, DK .
BLOOD, 1997, 89 (06) :1870-1875
[8]
ANGIOGENESIS IN CANCER, VASCULAR, RHEUMATOID AND OTHER DISEASE [J].
FOLKMAN, J .
NATURE MEDICINE, 1995, 1 (01) :27-31
[9]
FOLKMAN J, 1992, INFLAMMATION BASIC P, P809
[10]
Hussong JW, 2000, BLOOD, V95, P309