TY - JOUR
T1 - Fenugreek a naturally occurring edible spice as an anticancer agent
AU - Shabbeer, Shabana
AU - Sobolewski, Michelle
AU - Anchoori, Ravi Kumar
AU - Kachhap, Sushant
AU - Davidson, Nancy
AU - Carducci, Michael A.
AU - Khan, Saeed R.
N1 - Funding Information:
This work was supported by a research grant from the NCI SPORE Grant P50CA58236, Prostate Cancer Foundation, AEGON International Fellowship in Oncology and FAMRI.
PY - 2009/2
Y1 - 2009/2
N2 - In recent years, various dietary components that can potentially be used for the prevention and treatment of cancer have been identified. In this study, we demonstrate that extract (FE) from the seeds of the plant Trigonella foenum graecum, commonly called fenugreek, are cytotoxic in vitro to a panel of cancer but not normal cells. Treatment with 10-15 ug/mL of FE for 72 h was growth inhibitory to breast, pancreatic and prostate cancer cell lines (PCa). When tested at higher doses (15-20 ug/mL), FE continued to be growth inhibitory to PCa cell lines but not to either primary prostate or hTert-immortalized prostate cells. At least part of the growth inhibition is due to induction of cell death, as seen by incorporation of Ethidium Bromide III into cancer cells exposed to FE. Molecular changes induced in PCa cells are: in DU-145 cells: downregulation of mutant p53, and in PC-3 cells upregulation of p21 and inhibition of TGFβ induced phosphorylation of Akt. The surprising finding of our studies is that death of cancer cells occurs despite growth stimulatory pathways being simultaneously upregu-lated (phosphorylated) by FE. Thus, these studies add another biologically active agent to our armamentarium of naturally occurring agents with therapeutic potential.
AB - In recent years, various dietary components that can potentially be used for the prevention and treatment of cancer have been identified. In this study, we demonstrate that extract (FE) from the seeds of the plant Trigonella foenum graecum, commonly called fenugreek, are cytotoxic in vitro to a panel of cancer but not normal cells. Treatment with 10-15 ug/mL of FE for 72 h was growth inhibitory to breast, pancreatic and prostate cancer cell lines (PCa). When tested at higher doses (15-20 ug/mL), FE continued to be growth inhibitory to PCa cell lines but not to either primary prostate or hTert-immortalized prostate cells. At least part of the growth inhibition is due to induction of cell death, as seen by incorporation of Ethidium Bromide III into cancer cells exposed to FE. Molecular changes induced in PCa cells are: in DU-145 cells: downregulation of mutant p53, and in PC-3 cells upregulation of p21 and inhibition of TGFβ induced phosphorylation of Akt. The surprising finding of our studies is that death of cancer cells occurs despite growth stimulatory pathways being simultaneously upregu-lated (phosphorylated) by FE. Thus, these studies add another biologically active agent to our armamentarium of naturally occurring agents with therapeutic potential.
KW - Breast cancer
KW - Dietary bioactive agents
KW - Diosgenin
KW - Fenugreek
KW - Pancreatic cancer and phosphorylation
KW - Prostate cancer
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U2 - 10.4161/cbt.8.3.7443
DO - 10.4161/cbt.8.3.7443
M3 - Article
C2 - 19197146
AN - SCOPUS:77953333830
SN - 1538-4047
VL - 8
SP - 272
EP - 278
JO - Cancer Biology and Therapy
JF - Cancer Biology and Therapy
IS - 3
ER -