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Published on: June 26, 2018
Anticancer activity of Trigonella Foenumgraecum (fenugreek) seed extract by inducing apoptosis in pancreatic cancer
Nur Azizah Arryanie Binti Morshidi1, Md Salah Uddin2, Jungwhoi Lee3
1Department of Biotechnology, College of Applied Life Science, SARI, Jeju National University Jeju 63608, Republic of Korea.
Background/Aim:
Pancreatic cancer exhibits resistance to currently available drugs in the pharmaceutical industry. The development of new drugs is crucial, and research on plant substances with biological activities against cancer is actively underway. This study explored the potential use of fenugreek seed extract (FSE) in pancreatic cancer treatment as the anticancer activity of FSE is still poorly understood.
Materials And Methods:
The anticancer activity of FSE on pancreatic cancer cells was evaluated using cell viability and apoptosis assays. The migration rate of cancer cells was quantified using wound healing and Transwell migration assays. Western blotting was utilized to assess relevant signaling pathways, and LC-MS/MS was employed to detect the active compounds in FSE.
Results:
FSE inhibited the proliferation of pancreatic cancer cell lines (Panc-1, Miapaca-2, SNU-213, and Aspc-1) in a time and dose-dependent manner without greatly affecting normal cells (293T). The inhibition of cancer cell proliferation was attributed to the activation of cleaved caspase-3 and Bax, a pro-apoptotic marker. The anticancer effects and inhibition of cell migration were mediated by the MAPK, Akt, MMP-9, and vimentin signaling pathways through inactivation of the phosphorylated proteins related to cell growth, differentiation, and migration. LC-MS/MS analysis detected various active compounds capable of inducing apoptosis in pancreatic cancer cells.
Conclusion:
We demonstrated that FSE has anticancer properties by inducing apoptosis and preventing metastasis in pancreatic cancer cells without affecting normal cells.
Insights
Fenugreek seed extract (FSE) shows promise as a pancreatic cancer treatment. FSE effectively inhibits cancer cell growth and migration by inducing apoptosis, without harming normal cells.
Area of Science:
- Oncology
- Pharmacology
- Natural Products Chemistry
Background:
- Pancreatic cancer is highly resistant to existing pharmaceutical treatments, necessitating novel therapeutic strategies.
- Research into plant-derived compounds with anticancer properties is ongoing, with fenugreek seed extract (FSE) being a potential candidate.
- The precise anticancer mechanisms of FSE in pancreatic cancer remain largely uncharacterized.
Purpose of the Study:
- To investigate the potential of fenugreek seed extract (FSE) as a therapeutic agent against pancreatic cancer.
- To elucidate the cellular and molecular mechanisms underlying FSE's anticancer activity.
Main Methods:
- Evaluated FSE's impact on pancreatic cancer cell viability and apoptosis using specific assays.
- Quantified cancer cell migration using wound healing and Transwell assays.
- Assessed key signaling pathways (MAPK, Akt) and metastasis-related proteins (MMP-9, vimentin) via Western blotting.
- Identified active compounds in FSE using Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS).
Main Results:
- FSE significantly inhibited pancreatic cancer cell proliferation (Panc-1, Miapaca-2, SNU-213, Aspc-1) dose- and time-dependently.
- Normal cells (293T) showed minimal impact from FSE treatment.
- Anticancer effects were linked to apoptosis induction (cleaved caspase-3, Bax) and suppressed cell migration.
- FSE modulated MAPK, Akt, MMP-9, and vimentin pathways by inactivating key phosphorylated proteins.
Conclusions:
- Fenugreek seed extract demonstrates significant anticancer properties against pancreatic cancer cells.
- FSE effectively induces apoptosis and inhibits metastasis in pancreatic cancer models.
- The observed effects occur without significant toxicity to normal cells, highlighting FSE's therapeutic potential.
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