The selective cytotoxic anti-cancer properties and proteomic analysis of Trigonella Foenum-Graecum
© Alsemari et al.; licensee BioMed Central Ltd. 2014
Received: 8 July 2013
Accepted: 6 March 2014
Published: 29 March 2014
There are a number of dietary components that may prove useful in the prevention and treatment of cancer. In some cultures, fenugreek seeds are used to treat cancer. The current study focuses on the anticancer properties and proteomic profiles of fenugreek seeds, and is prompted by the clinical profile of a case of primary CNS T cell lymphoma that responded to fenugreek treatment and resulted in tumor regression.
Various normal and cancer cell lines were exposed to fenugreek extract at differing concentrations (100 μg/ml, 200 μg/ml and 300 μg/ml) and at different time points (0, 24, 48, 72 and 96 hrs). Protein fingerprints of fenugreek grain/seed types, obtained from four different geographical regions, were analyzed by proteomic expression profiles.
We observed selective cytotoxic effects of fenugreek extract in vitro to a panel of cancer cell lines, including T-cell lymphoma. Additionally, the cluster analysis of proteomics data showed that the protein profile of the particular fenugreek used by the patient is significantly different from three other regional subtypes of fenugreek extract.
The in vitro effect of fenugreek as a substance with significant cytotoxicity to cancer cells points to the potential usefulness of fenugreek in the prevention and treatment of cancer.
KeywordsPrimary T-cell lymphoma Cerebellum T-lymphocytes cells Trigonella foenum graecum (fenugreek) Brain tumor Proteomics Hierarchical cluster analysis/protein expression Anti-cancer
There is growing use of complementary and alternative anticancer medicines worldwide. Trigonella foenum graecum (fenugreek) is traditionally applied to treat disorders such as diabetes, high cholesterol, wound inflammation, and gastrointestinal ailments. Fenugreek is also reported to have anticancer properties due to its beneficial active chemical constituents. It’s mechanism of action is similar to several anticancer drugs, and is based on an ability to induce apoptosis.
In this report we demonstrate the selective cytotoxic effects of fenugreek extract in vitro on a panel of cancer cell lines, and a proteomics analysis of fenugreek.
The patient consented for the publication of the clinical report. The study was approved by the Office of Research Affairs (ORA under the umbrella of Research Advisory Council (RAC) of King Faisal Specialist Hospital and Research Center (KFSHRC), with approval umber RAC#. 2120 006.
In order to avoid sample source variability all samples analyzed were purchased from the same local grocery store used by the patient.
Cell culture and fenugreek extraction
A variety of normal and cancer cell lines including; T-cell lymphoma (TCP), B-cell lymphomas, Thyroid Papillary carcinoma (FRO) and human breast cancer (MCF7) were obtained from American Type Culture Collection (ATCC). Cells were cultivated at 37°C and 5% CO2 in Dulbecco’s MEM (DMEM) containing 5% fetal bovine serum, 3 mM glutamine (Gibco, NJ, USA) and antibiotics.
Fenugreek seeds were extracted in water, filtered, and concentrated with minor modification. The extract was reconstituted to a working stock concentration of 50 mg/ml. Cells were exposed to fenugreek extract at different concentrations (100 ug/ml, 200 ug/ml and 300 ug/ml) and at different time points (0, 24, 48, 72 and 96 hrs).
Cell viability assay
Cells were seeded onto a 96-well plate at a density of 5000 cells/well. In order to achieve meaningful quantitative analysis, duplicate or triplicates samples were subsequently incubated at 37°C for 72 hrs. in a titrated medium containing different concentrations of fenugreek extract. The number of viable cells was estimated using the protocol of 3-(4,5-dimethylthazol-2yl)-2,5-diphenyletrazlium bromide (MTT)-assay (Promega, Madison, WI, USA).
Apoptosis analysis by annexin V staining
Approximately 5 × 105 cells were seeded and cultured in 60 mm plates to 50-70% confluence. Triplicate samples were subsequently incubated at 37°C for 72 hours in a titrated medium containing different concentrations of fenugreek extract. The applied fenugreek extract was re-constituted in sterile water to yield the desired concentration of 300 ug/ml. Cells were collected at 24, 48, 72 and 96 hours, centrifuged and re-suspended in 1 ml of PBS. Thereafter, cells were stained with Propidium Iodide (PI) and Alexa Fluor 488 Annexin V, using Vybrant Apoptosis Assay kit #2 (molecular probes) according to the manufacturer’s protocol. Stained cells were analyzed by flow cytometry. Viable cell percentages were determined by the FACS Calibur apparatus and the Cell Quest Pro software from Becton Dickinson (BD Biosciences).
Proteomics analysis of anticancer effects of fenugreek proteins on brain tumor
Protein patterns of different types of fenugreek grains/seeds were obtained from four different regions (labeled A-D). All four fenugreek types were analyzed by two-dimensional polyacrylamide gel electrophoresis (2-DE) for global differential protein expression profiles. The aim was to identify significantly differentially expressed proteins, and to identify proteins that are cancer related amongst the four types. The potential clinical applications of these proteins will be further evaluated.
Electrophoresis, scanning and image analysis
Seeds/grains from four different fenugreek types were ground and protein extracted. The samples were diluted to a total volume of 350 μl, in a solution containing 8 M urea, 2 M thio urea, 0.2% Pharmalyte, 0.3% DTT, 2 M CHAPS and a trace of bromphenol blue. A total amount of 75 μg of protein was loaded on each strip via rehydration using linear pH 4–7 Ready IPG, strips (Bio-Rad, Hercules, CA, USA). First-dimension isoelectric focusing was carried out for a total of 45,500 Vh in a PROTEAN IEF cell (Bio-Rad).
The IPG-strips were then loaded and run on a 12.5% SDS-PAGE gel overnight at 100 V (constant) until the bromophenol blue dye front had reached the bottom of the gel. The gels were stained with silver nitrate and scanned using a calibrated densitometer, GS 800 and data was analyzed using PDQUEST software (Bio-Rad). Between 3–4 gels were run from each sample to allow for significant statistical analysis and ensure sample reproducibility.
Data preprocessing/data analysis
A difference of ≥ 2-fold change was used as a threshold for marked quantitative difference between pairs of samples. Significantly differentially expressed protein spots were first selected using two different statistical methods (Student’s t test and Partial Least Square analysis), features available in PDQuest 2-DE image analysis software. The data from the match set was exported from PDQUEST in the form of a data table, with rows representing gels and columns representing spots. Datasets were normalized prior to analysis[10, 11]. The resulting data were subjected to hierarchical clustering analysis using the J Express software (java.sun.com).
Cytotoxic effect of fenugreek on normal and cancer cells
We found that fenugreek extract has a very selective cytotoxicity against cancer cell lines such as T-cell lymphoma (TCP), B-cell lymphomas, Thyroid Papillary carcinoma (FRO) and breast cancer (MCF7). On the other hand, there was no significant cell cytotoxicity amongst normal cells, including human lymphocytes and meningioma, when treated with fenugreek. This clearly indicates that fenugreek has selective cytotoxic effects against cancer cells (Additional file3: Figure S3).
Fenugreek selectively induces apoptosis in cancer and normal cells
Comparison of protein expression patterns between the four regional fenugreek samples
Hierarchical cluster analysis of differentially expressed proteins between the four regional fenugreek samples
Some of the differentially expressed protein spots, that are absent or down-regulated in the fenugreek A samples compared with the remaining three fenugreek types, are shown in Additional file7: Figure S6. On the other hand, the up-regulated protein spots in the fenugreek A samples, as compared to the other fenugreek samples, are shown as gel segments in Additional file8: Figure S7AB.
The clustering data, taken together with the correlation analyses of protein expression patterns, showed clearly that three fenugreek types (B/C/D) were very similar (average correlation coefficient = 0.86) compared with fenugreek A (r = 0.38). This indicates that even though there might be different fenugreek species, the medicinal properties they possess may be due to specific proteins that span the regional/species differences.
Despite the rarity of T-cell lymphomas, primary CNS lymphoma has a, distinctive clinical presentation[12–17], and has a poor prognosis. The standard first-line treatment, of radiation therapy and chemotherapy, can achieve a complete response in only 20%–50% of patients. And the reported median survival for T-cell CNS lymphomas is between 13.5 and 22 months[17, 19].
Our case study, to our knowledge, is the first of its kind to show the anticancer properties of fenugreek in a patient with established relapsed primary CNS lymphoma. The daily use of aqueous extract of fenugreek resulted in 11 years remission of relapsed primary CNS T- cell lymphoma. Also our experimental research, in vitro, showed that fenugreek is also selectively cytotoxic to cancer, and not to normal cells. Normal lymphocytes showed no apoptosis while T-Cell lymphoma and breast cancer cells were highly apoptotic following fenugreek treatment.
There is a clear reciprocal in vivo and in vitro anti cancer response to aqueous fenugreek. The distinctive, long duration, remission of a patient with relapsed primary T-cell lymphoma after daily use of aqueous extract of a particular Trigonella foenum graecum, however remarkable, only represents a single case. A more rigorous scientific evaluation, such as a clinical trial, is obviously warranted before the anti cancer properties of fenugreek can be confirmed
Nonetheless, alternative medicine use is widespread amongst cancer patients. In many surveys, herbal medicines are amongst the most commonly used treatments. Herbal remedies are believed by the general public to be safe, cause less side-effects and be less likely to cause dependency. However most of these perceptions have not been studied in prospective research.
Extracts of fenugreek seeds, and some of their constituents, have been shown to have anti carcinogenic potency[21–23]. Anti cancer properties of fenugreek, or its constituents, involve multiple functional and molecular targets. Fenugreek induced apoptosis has been reported in a wide variety of tumor cell lines including human; colon, osteosarcoma, leukemia, breast, and liver.
The preventive efficacy of dietary fenugreek seed, and its major constituent, diosgenin, on azoxymethane-induced rat colon carcinogenesis during initiation and promotion stages has been evaluated. These in vitro experiments indicated that diosgenin inhibits cell growth and induces apoptosis in the HT-29 human colon cancer cell line in a dose-dependent manner. Furthermore, diosgenin induced apoptosis in HT-29 cells at least in part by inhibition of bcl-2 and by induction of caspase-3 protein expression. This study suggests the fenugreek constituent, diosgenin, has potential as a novel preventive agent for colon cancer.
Another study suggested significant chemo preventive effect of fenugreek seeds against breast cancer. Fenugreek seed extract was demonstrated to significantly inhibit MDA 231-induced mammary hyperplasia and decreased its incidence. The authors further suggest that apoptosis might mediate fenugreek’s protective anti-breast cancer effects. The induction of apoptosis by fenugreek extract is suggested by its ability to increase the expression of pro-apoptotic genes, and thus this spice holds promise for consideration in complementary therapy for breast cancer.
In a recent study, fenugreek was demonstrated to be cytotoxic to a panel of cancer but not normal cells. Treatment with 10–15 μg/mL of fenugreek for 72 h was found to be growth inhibitory to breast, pancreatic and prostate cancer cell lines. When tested at higher doses (15–20 μg/mL), fenugreek continued to be growth inhibitory to prostate cancer cell lines but not to either primary prostate or normal prostate cell lines. At least part of the growth inhibition was reported to be due to induction of cell death, as seen by incorporation of Ethidium Bromide III into cancer cells exposed to fenugreek.
Protodioscin (PD) has been purified from fenugreek and identified by Mass, and 1H- and 13C NMR. The effects of PD on cell viability in human leukemia (HL-60) and human stomach cancer (KATO III) cells have been investigated. PD displayed strong growth inhibitory effect against HL-60 cells, but weak growth inhibitory effect on KATO III cells. Morphological changes (apoptotic bodies) have been observed in HL-60 cells treated with PD, but not in KATO III cells treated with PD. These findings suggest that growth inhibition of HL-60 cells by PD results from the induction of apoptosis.
Al-daghri reported that incubation of Jurkat T lymphocytes cells with fenugreek extract at concentrations ranging from 30 to 1500 μg/mL, for up to 3 days resulted in cell death in a dose- and time-dependent manner. Jurkat cell death was preceded by the appearance of multiple large vacuoles, which coincided with transcriptional up-regulation of the autophagy marker LC3. Distinct morphological changes including the appearance of large vacuoles, membrane disintegration and increased expression of autophagy protein LC3 transcripts indicated that fenugreek extract induced autophagy and autophagy-associated death of Jurkat cells.
Autophagy is a physiological response to stress and has been suggested to enable cells to adapt and survive and, hence, is considered a pro-survival mechanism. Apoptosis is the best-described form of programmed cell death, but autophagy reportedly contributes to cell death as well. It has also been defined as an extremely conserved process of programmed cell death and its activation causes cell death. Defective regulation of autophagy in cancers suggests that autophagy is a true tumor suppressor pathway.
It has been suggested that environmental and geographical differences may significantly influence the biologically active components of fenugreek extracts. In our study, four different types of fenugreek were analyzed by proteomics fingerprinting. A set of eight protein spots from fenugreek seeds obtained from one particular region (A) were significantly different from those harvested from three different geographical locations (B, C & D). Our proteomics data, based on these eight protein spots, allowed accurate discrimination between regional fenugreek A and three other fenugreek samples B, C and D.
These proteins are of significant interest, and thus warrant further characterization to more fully explore their potential therapeutic use. We recognize the limited sample size of this preliminary study, however our results are of significant interest as they highlight the potential usefulness of a particular type of fenugreek as an anti-cancer drug. However, these exciting results obviously warrant additional study, including further drug characterization and development.
In summary, to our knowledge, this is the first human case in which established malignant CNS cancer showed regression, then disappearing of the cancer lesion with daily use of fenugreek extract. Fenugreek may serve as a potential therapeutic in the treatment of lymphoid malignancy and other cancers. GC-MS analysis of fenugreek extract indicated the presence of several compounds with anticancer properties, including gingerol, cedrene, zingerone, vanillin and eugenol. However whole crude extract has been shown to provide more selective potential than these individual compounds used in isolation. Also it must be considered that the biologically active agents in fenugreek may vary based on geographical environments.
We acknowledge the support of grants from King Faisal Specialist Hospital and Research Centre.
- Losso JN, Holliday DL, Finley JW, Martin RJ, Rood JC, Yu Y, Greenway FL: Fenugreek bread: a treatment for diabetes mellitus. J Med Food. 2009, 12 (5): 1046-1049.View ArticlePubMedGoogle Scholar
- Sharma RD, Raghuram TC, Rao NS: Effect of fenugreek seeds on blood glucose and serum lipids in type I diabetes. Eur J Clin Nutr. 1990, 44 (4): 301-306.PubMedGoogle Scholar
- Uemura T, Hirai S, Mizoguchi N, Goto T, Lee JY, Taketani K, Nakano Y, Shono J, Hoshino S, Tsuge N, Narukami T, Takahashi N, Kawada T: Diosgenin present in fenugreek improves glucose metabolism by promoting adipocyte differentiation and inhibiting inflammation in adipose tissues. Mol Nutr Food Res. 2010, 54 (11): 1596-608.View ArticlePubMedGoogle Scholar
- Pandian RS, Anuradha CV, Viswanathan P: Gastroprotective effect of fenugreek seeds (Trigonella foenum graecum) on experimental gastric ulcer in rats. J Ethnopharmacol. 2002, 81 (3): 393-397.View ArticlePubMedGoogle Scholar
- Khoja KK, Shaf G, Hasan TN, Syed NA, Al-Khalifa AS, Al-Assaf AH, Alshatwi AA: Fenugreek, a naturally occurring edible spice, kills MCF-7 human breast cancer cells via an apoptotic pathway. Asian Pac J Cancer Prev. 2011, 12 (12): 3299-3304.PubMedGoogle Scholar
- al-Ghamdi H, Sabbah R, Martin J, Patay Z: Primary T-cell lymphoma of the brain in children: a case report and literature review. Pediatr Hematol Oncol. 2000, 17 (4): 341-343.View ArticlePubMedGoogle Scholar
- Ali L, Azad Khan AK, Hassan Z, Mosihuzzaman M, Nahar N, Nasreen T, Nur-e-Alam M, Rokeya B: Characterization of the hypoglycemic effects of Trigonella foenum graecum seed. Planta Med. 1995, 61 (4): 358-360.View ArticlePubMedGoogle Scholar
- Navayath S, Thiyagarajan D: Fenugreek supplementation imparts erythrocyte resistance to cypermethrin induced oxidative changes in vivo. J Complement Integr Med. 2011, 8:Google Scholar
- Al-Johar D, Shinwari N, Arif J, Al-Sanea N, Jabbar AA, El-Sayed R, Mashhour A, Billedo G, El-Doush I, Al-Saleh I: Role of Nigella sativa and a number of its antioxidant constituents towards azoxymethane-induced genotoxic effects and colon cancer in rats. Phytother Res. 2008, 22 (10): 1311-1323.View ArticlePubMedGoogle Scholar
- Alaiya AA, Franzen B, Hagman A, Dysvik B, Roblick UJ, Becker S, Moberger B, Auer G, Linder S: Molecular classification of borderline ovarian tumors using hierarchical cluster analysis of protein expression profiles. Int J Cancer. 2002, 98 (6): 895-899.View ArticlePubMedGoogle Scholar
- Alaiya AA, Franzen B, Hagman A, Silfversward C, Moberger B, Linder S, Auer G: Classification of human ovarian tumors using multivariate data analysis of polypeptide expression patterns. Int J Cancer. 2000, 86 (5): 731-736.View ArticlePubMedGoogle Scholar
- Grant JW, Isaacson PG: Primary central nervous system lymphoma. Brain Pathol. 1992, 2 (2): 97-109.View ArticlePubMedGoogle Scholar
- Bednar MM, Salerni A, Flanagan ME, Pendlebury WW: Primary central nervous system T-cell lymphoma. Case report. J Neurosurg. 1991, 74 (4): 668-672.View ArticlePubMedGoogle Scholar
- Knorr JR, Ragland RL, Stone BB, Woda BA, Gelber ND: Cerebellar T-cell lymphoma: an unusual primary intracranial neoplasm. Neuroradiology. 1992, 35 (1): 79-81.View ArticlePubMedGoogle Scholar
- Grant JW, von Deimling A: Primary T-cell lymphoma of the central nervous system. Arch Pathol Lab Med. 1990, 114 (1): 24-27.PubMedGoogle Scholar
- Morgello S, Maiese K, Petito CK: T-cell lymphoma in the CNS: clinical and pathologic features. Neurology. 1989, 39 (9): 1190-1196.View ArticlePubMedGoogle Scholar
- Shenkier TN1, Blay JY, O’Neill BP, Poortmans P, Thiel E, Jahnke K, Abrey LE, Neuwelt E, Tsang R, Batchelor T, Harris N, Ferreri AJ, Ponzoni M, O’Brien P, Rubenstein J, Connors JM: Primary CNS lymphoma of T-cell origin: a descriptive analysis from the international primary CNS lymphoma collaborative group. J Clin Oncol. 2005, 23 (10): 2233-2239.View ArticlePubMedGoogle Scholar
- Latta S, Myint ZW, Jallad B, Hamdi T, Alhosaini MN, Kumar DV, Kheir F: Primary central nervous system T-cell lymphoma in aids patients: case report and literature review. Curr Oncol. 2010, 17 (5): 63-66.View ArticlePubMedPubMed CentralGoogle Scholar
- Abrey LE, Yahalom J, DeAngelis LM: Treatment for primary CNS lymphoma: the next step. J Clin Oncol. 2000, 18 (17): 3144-3150.PubMedGoogle Scholar
- Olaku O, White JD: Herbal therapy use by cancer patients: a literature review on case reports. Eur J Cancer. 2011, 47 (4): 508-514.View ArticlePubMedGoogle Scholar
- Hibasami H, Moteki H, Ishikawa K, Katsuzaki H, Imai K, Yoshioka K, Ishii Y, Komiya T: Protodioscin isolated from fenugreek (Trigonella foenumgraecum L.) induces cell death and morphological change indicative of apoptosis in leukemic cell line H-60, but not in gastric cancer cell line KATO III. Int J Mol Med. 2003, 11 (1): 23-26.PubMedGoogle Scholar
- Sur P, Das M, Gomes A, Vedasiromoni JR, Sahu NP, Banerjee S, Sharma RM, Ganguly DK: Trigonella foenum graecum (fenugreek) seed extract as an antineoplastic agent. Phytother Res. 2001, 15 (3): 257-259.View ArticlePubMedGoogle Scholar
- Shabbeer S, Sobolewski M, Anchoori RK, Kachhap S, Hidalgo M, Jimeno A, Davidson N, Carducci MA, Khan SR: Fenugreek: a naturally occurring edible spice as an anticancer agent. Cancer Biol Ther. 2009, 8 (3): 272-278.View ArticlePubMedPubMed CentralGoogle Scholar
- Raju J, Patlolla JM, Swamy MV, Rao CV: Diosgenin, a steroid saponin of Trigonella foenum graecum (Fenugreek), inhibits azoxymethane-induced aberrant crypt foci formation in F344 rats and induces apoptosis in HT-29 human colon cancer cells. Cancer Epidemiol Biomarkers Prev. 2004, 13 (8): 1392-1398.PubMedGoogle Scholar
- Corbiere C, Liagre B, Bianchi A, Bordji K, Dauca M, Netter P, Beneytout JL: Different contribution of apoptosis to the antiproliferative effects of diosgenin and other plant steroids, hecogenin and tigogenin, on human 1547 osteosarcoma cells. Int J Oncol. 2003, 22 (4): 899-905.PubMedGoogle Scholar
- Liu MJ, Wang Z, Ju Y, Wong RN, Wu QY: Diosgenin induces cell cycle arrest and apoptosis in human leukemia K562 cells with the disruption of Ca2+ homeostasis. Cancer Chemother Pharmacol. 2005, 55 (1): 79-90.View ArticlePubMedGoogle Scholar
- Srinivasan S, Koduru S, Kumar R, Venguswamy G, Kyprianou N, Damodaran C: Diosgenin targets Akt-mediated prosurvival signaling in human breast cancer cells. Int J Cancer. 2009, 125 (4): 961-967.View ArticlePubMedGoogle Scholar
- Li F, Fernandez PP, Rajendran P, Hui KM, Sethi G: Diosgenin, a steroidal saponin, inhibits STAT3 signaling pathway leading to suppression of proliferation and chemosensitization of human hepatocellular carcinoma cells. Cancer Lett. 2010, 292 (2): 197-207.View ArticlePubMedGoogle Scholar
- Amin A, Alkaabi A, Al-Falasi S, Daoud SA: Chemopreventive activities of Trigonella foenum graecum (Fenugreek) against breast cancer. Cell Biol Int. 2005, 29 (8): 687-694.View ArticlePubMedGoogle Scholar
- Al-Daghri NM, Alokail MS, Alkharfy KM, Mohammed AK, Abd-Alrahman SH, Yakout SM, Amer OE, Krishnaswamy S: Fenugreek extract as an inducer of cellular death via autophagy in human T lymphoma Jurkat cells. BMC Complement Altern Med. 2012, 12: 202-View ArticlePubMedPubMed CentralGoogle Scholar
- Chen N, Debnath J: Autophagy and tumorigenesis. FEBS Lett. 2010, 584 (7): 1427-1435.View ArticlePubMedGoogle Scholar
- Vicencio JM1, Galluzzi L, Tajeddine N, Ortiz C, Criollo A, Tasdemir E, Morselli E, Ben Younes A, Maiuri MC, Lavandero S, Kroemer G: Senescence, apoptosis or autophagy? When a damaged cell must decide its path--a mini-review. Gerontology. 2008, 54 (2): 92-99.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6882/14/114/prepub
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