Generic placeholder image

The Natural Products Journal

Editor-in-Chief

ISSN (Print): 2210-3155
ISSN (Online): 2210-3163

Research Article

Antioxidant and Cytotoxicity Activity of Phenolic Compounds from Piper sarmentosum Roxb. Against T47D Human Breast Cancer Cell

Author(s): Nor Farahiyah Ghazali*, Farah Farisha Mustafa, Tengku Sifzizul Tengku Muhammad and Maizatul Akma Ibrahim

Volume 10, Issue 4, 2020

Page: [364 - 371] Pages: 8

DOI: 10.2174/2210315509666190621161445

Price: $65

Abstract

Background: Cancer is a major public health burden worldwide. Breast cancer tops the chart as the most common cancer of today and has become the major cause of death inthe female population. Approximately 60% of currently applied cancer drugs are derived from natural sources. Piper sarmentosum Roxb. is one of the natural plants that had been traditionally used as herbal medicine. Phytochemical compounds from this plant were reported to be important in the promotion of human health, mainly due to its phenolic compounds, which have been linked with various biomedical properties.

Objective: To identify the phenolic profile of P. sarmentosum leaves methanolic extract and to investigate the antioxidant and cytotoxicity activity on human breast carcinoma cells, T47D.

Methods: Methanolic extract of P. sarmentosum leaves was analyzed by using Folin-Ciocalteu method and High Performance Liquid Chromatography (HPLC). In vitro antioxidant study of the extract was carried out using diphenylpicrylhydrazyl (DPPH) scavenging test. In vitro cytotoxicity assay was conducted by using 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4- sulfophenyl)-2H-tetrazolium (MTS) assay. Biochemical test of DNA fragmentation was also applied to study the extract’s cytotoxicity effect on T47D mode of cell death.

Results: The Total Phenolic Content (TPC) for the P. sarmentosum extract was 89.33 mg GAE/g DM and HPLC revealed the presence of flavonoids and phenolic acids. From the DPPH assay, P. sarmentosum extract exhibited antioxidant activity with the EC50 at 60.24 μg/mL. The cytotoxicity analysis by MTS assay showed the treatment of T47D cells with the plant extract that caused cytotoxic effect on the cells, with an IC50 value of 2.69 μg/mL. The DNA fragmentation assay on the extract- treated T47D cells exhibited internucleosomal DNA fragmentation of the cell's genome on an electrophoresis agarose gel.

Conclusion: The phenolic compounds identified from P. sarmentosum have cytotoxic effects against breast cancer cells, T47D. These compounds could be a promising anticancer agent candidate for breast cancer treatment. Further studies on the isolation, structural elucidation and mechanism of action on the active compounds are required prior to in vivo and clinical study.

Keywords: Piper sarmentosum, breast cancer, phenolic compounds, antioxidant, cytotoxicity, T47D cells.

Graphical Abstract

[1]
Chia, Y.Y.; Kanthimathi, M.S.; Rajarajeswaran, J.; Khoo, K.S.; Cheng, H.M. Antioxidant, antiproliferative, genotoxic and cytoprotective effects of the methanolic extract of Padina tetrastromatica on human breast adenocarcinoma and embryonic fibroblast cell lines. Front. Life Sci., 2015, 8(4), 411-418.
[http://dx.doi.org/10.1080/21553769.2015.1051245]
[2]
Colditz, G. A.; Bohlke, K. Preventing breast cancer now by acting on what we already know. Nat. Partn. J., 2015, 1(1)
[3]
Rajendran, S.; Saravanan, R.; Ramalingam, S.; Shahul Hameed, S.A. Antiproliferative and antioxidant activity of Gynandropsis pentaphylla linn on MCF-7 cell line. Int. J. Pharm. Pharm. Sci., 2014, 6(7), 561-565.
[4]
Sriwiriyajan, S.; Ninpesh, T.; Sukpondma, Y.; Nasomyon, T.; Graidist, P. Cytotoxicity screening of plants of genus Piper in breast cancer cell lines. Trop. J. Pharm. Res., 2014, 13(6), 921-928.
[http://dx.doi.org/10.4314/tjpr.v13i6.14]
[5]
Vijayalakshmi, A.; Kumar, P.R.; Sakthi Priyadarsini, S.; Meenaxshi, C. In vitro antioxidant and anticancer activity of flavonoid fraction from the aerial parts of Cissus Quadrangularis Linn. against human breast carcinoma cell lines. J. Chem., 2013, 2013, 1-9.
[http://dx.doi.org/10.1155/2013/150675]
[6]
Akim, A.; Ling, L.C.; Rahmat, A.; Zakaria, Z.A. Antioxidant and anti-proliferative activities of roselle juice on CAOV-3, MCF-7, MDA-MB-231 and HELA cancer cell lines. Afr. J. Pharm. Pharmacol., 2011, 5(7), 957-965.
[7]
Maftei, C.V.; Fodor, E.; Jones, P.G.; Freytag, M.; Franz, M.H.; Kelter, G.; Fiebig, H-H.; Tamm, M.; Neda, I. N-heterocyclic carbenes (NHC) with 1,2,4-oxadiazole-substituents related to natural products: Synthesis, structure and potential antitumor activity of some corresponding gold(I) and silver(I) complexes. Eur. J. Med. Chem., 2015, 101, 431-441.
[http://dx.doi.org/10.1016/j.ejmech.2015.06.053] [PMID: 26185007]
[8]
Maftei, C.V.; Fodor, E.; Jones, P.G.; Daniliuc, C.G.; Franz, M.H.; Kelter, G.; Fiebig, H.H.; Tamm, M.; Neda, I. Novel 1,2,4-oxadiazoles and trifluoromethylpyridines related to natural products: Synthesis, structural analysis and investigation of their antitumor activity. Tetrahedron, 2016, 72(9), 1185-1199.
[http://dx.doi.org/10.1016/j.tet.2016.01.011]
[9]
Neda, I.; Kaukorat, T.; Schmutzler, R.; Niemeyer, U.; Kutscher, B.; Pohl, J.; Engel, J. Benzodiaza-, benzoxaza-, and benzodioxaphosphorinones - Formation, reactivity, structure, and biological activity. Phosphorus Sulfur Silicon Relat. Elem., 2000, 162(1), 81-218.
[http://dx.doi.org/10.1080/10426500008045221]
[10]
Mihorianu, M.; Franz, M.H.; Jones, P.G.; Freytag, M.; Kelter, G.; Fiebig, H.H.; Tamm, M.; Neda, I. N-heterocyclic carbenes derived from imidazo-[1,5-a]pyridines related to natural products: synthesis, structure and potential biological activity of some corresponding gold (I) and silver (I). Complexes. Appl. Organomet. Chem., 2016, 30(7), 581-589.
[http://dx.doi.org/10.1002/aoc.3474]
[11]
Do, Q.D.; Angkawijaya, A.E.; Tran-Nguyen, P.L.; Huynh, L.H.; Soetaredjo, F.E.; Ismadji, S.; Ju, Y-H.; Diem, Q.; Elisa, A.; Tran-Nguyen, P.L. Effect of extraction solvent on total phenol content, total flavonoid content, and antioxidant activity of Limnophila aromatica. Yao Wu Shi Pin Fen Xi, 2014, 22(3), 296-302.
[http://dx.doi.org/10.1016/j.jfda.2013.11.001] [PMID: 28911418]
[12]
Chan, E.W.C.; Wong, S.K. Phytochemistry and pharmacology of three Piper species: An update. Int. J. Pharmacogn., 2014, 1(9), 534-544.
[13]
Syed Ab Rahman, S.F.; Sijam, K.; Omar, D.; Abd Wahab, M.Z. Identification of phenolic compounds and evaluation of antibacterial properties of Piper sarmentosum roxb against rice pathogenic bacteria. Malays. J. Microbiol., 2016, 12(6), 475-484.
[14]
Ugusman, A.; Zakaria, Z.; Hui, C.K.; Nordin, N.A.M.M.; Mahdy, Z.A. Flavonoids of Piper sarmentosum and its cytoprotective effects against oxidative stress. EXCLI J., 2012, 11, 705-714.
[PMID: 27847456]
[15]
Hussain, K.; Ismail, Z.; Sadikun, A.; Ibrahim, P. Cytoxicity evaluation and characterization of leaf chloroform extract of Piper sarmentosum possessing antiangiogenic activity. Pharmacologyonline, 2009, 2, 379-391.
[16]
Atiax, E.; Ahmad, F.; Sirat, H.M.; Arbain, D. Antibacterial activity and cytotoxicity screening of Sumatran Kaduk (Piper Sarmentosum Roxb). Iran. J. Pharmacol. Ther., 2011, 10(1), 1-5.
[17]
Ali, A.A.; Suhaimi, F.; Mohd Saad, Q.; Mohd Fahami, N.A. Effects of Piper sarmentosum water extract on 11-β hydroxysteroid dehydrogenase type 1 bioactivity in ovariectomy-induced obese rats. Int. J. Pharmacol., 2009, 5(6), 362-369.
[http://dx.doi.org/10.3923/ijp.2009.362.369]
[18]
Rahman, N.; Noor, K.; Hlaing, K.; Suhaimi, F.; Kutty, M.; Sinor, M. Piper sarmentosum influences the oxidative stress involved in experimental diabetic rats. Internet J. Herb. Plant Med., 2010, 2(1), 1-8.
[19]
Syed Ab Rahman, S.F.; Sijam, K.; Omar, D.; Ab Rahman, S.F.S.; Sijam, K.; Omar, D.; Syed Ab Rahman, S.F.; Sijam, K.; Omar, D. Identification and antibacterial activity of phenolic compounds in crude extracts of Piper sarmentosum (Kadok). J. Pure Appl. Microbiol., 2014, 8(2), 483-490.
[20]
Routray, W.; Orsat, V. Microwave-assisted extraction of flavonoids: A review. Food Bioprocess Technol., 2012, 5(2), 409-424.
[http://dx.doi.org/10.1007/s11947-011-0573-z]
[21]
Lee, K.H.; Padzil, A.M.; Syahida, A.; Abdullah, N.; Zuhainis, S.W.; Maziah, M.; Sulaiman, M.R.; Israf, D.A.; Shaari, K.; Lajis, N.H. Evaluation of anti-inflammatory, antioxidant and anti- nociceptive activities of six Malaysian medicinal plants. J. Med. Plants Res., 2011, 5(23), 5555-5563.
[22]
Fani, S.; Kamalidehghan, B.; Lo, K.M.; Nigjeh, S.E.; Keong, Y.S.; Dehghan, F.; Soori, R.; Abdulla, M.A.; Chow, K.M.; Ali, H.M.; Hajiaghaalipour, F.; Rouhollahi, E.; Hashim, N.M. Anticancer activity of a monobenzyltin complex C1 against MDA-MB-231 cells through induction of apoptosis and inhibition of breast cancer stem cells. Sci. Rep., 2016, 6(1), 38992.
[http://dx.doi.org/10.1038/srep38992] [PMID: 27976692]
[23]
Junqueira-Gonçalves, M.P.; Yáñez, L.; Morales, C.; Navarro, M.A.; Contreras, R.; Zúñiga, G.E. Isolation and characterization of phenolic compounds and anthocyanins from Murta (Ugni molinae Turcz.) fruits. Assessment of antioxidant and antibacterial activity. Molecules, 2015, 20(4), 5698-5713.
[http://dx.doi.org/10.3390/molecules20045698] [PMID: 25838172]
[24]
Pereira, R.M.S.; Andrades, N.E.D.; Paulino, N.; Sawaya, A.C.H.F.; Eberlin, M.N.; Marcucci, M.C.; Favero, G.M.; Novak, E.M.; Bydlowski, S.P. Synthesis and characterization of a metal complex containing naringin and Cu, and its antioxidant, antimicrobial, anti-inflammatory and tumor cell cytotoxicity. Molecules, 2007, 12(7), 1352-1366.
[http://dx.doi.org/10.3390/12071352] [PMID: 17909491]
[25]
Chan, G.K.Y.; Kleinheinz, T.L.; Peterson, D.; Moffat, J.G. A simple high-content cell cycle assay reveals frequent discrepancies between cell number and ATP and MTS proliferation assays. PLoS One, 2013, 8(5)e63583
[http://dx.doi.org/10.1371/journal.pone.0063583] [PMID: 23691072]
[26]
Alsabri, S.G.; El-Basir, H.M.; Rmeli, N.B.; Mohamed, S.B.; Allafi, A.A.; Zetrini, A.A.; Salem, A.A.; Mohamed, S.S.; Gbaj, A.; El-Baseir, M.M. Phytochemical screening, antioxidant, antimicrobial and anti-proliferative activities study of Arbutus pavarii plant. J. Chem. Pharm. Res., 2013, 5(1), 32-36.
[27]
Rayan, A.; Raiyn, J.; Falah, M. Nature is the best source of anticancer drugs: Indexing natural products for their anticancer bioactivity. PLoS One, 2017, 12(11) e018792.5
[http://dx.doi.org/10.1371/journal.pone.0187925] [PMID: 29121120]
[28]
Hussain, K.; Hashmi, F.K.; Latif, A.; Ismail, Z.; Sadikun, A.; Hashmi, K.; Latif, A.; Ismail, Z.; Sadikun, A.; Hashmi, F.K. A review of the literature and latest advances in research of Piper sarmentosum. Pharm. Biol., 2012, 50(8), 1045-1052.
[http://dx.doi.org/10.3109/13880209.2011.654229] [PMID: 22486533]
[29]
Zainal Ariffin, S.H.; Wan Omar, W.H.H.; Zainal Ariffin, Z.; Safian, M.F.; Senafi, S.; Megat Abdul Wahab, R. Intrinsic anticarcinogenic effects of Piper sarmentosum ethanolic extract on a human hepatoma cell line. Cancer Cell Int., 2009, 9(6), 6.
[http://dx.doi.org/10.1186/1475-2867-9-6] [PMID: 19257877]
[30]
Ee, G.C.L.; Lim, C.M.C.K.C.M.; Lim, C.K.; Rahmani, M.; Shaari, K.; Bong, C.F.J.; Kiang, L.C.; Taylor, P. Alkaloids from Piper sarmentosum and Piper nigrum. Nat. Prod. Res., 2009, 23(15), 1416-1423.
[http://dx.doi.org/10.1080/14786410902757998] [PMID: 19809914]
[31]
Lim, C.M. Identification of alkaloids of pepper (Piper nigrum) and kadok (Piper sarmentosum) and the biotransformation of piperine using Aspergillus niger., PhD Thesis, School of Graduate Studies, Universiti Putra Malaysia: Seri Kembangan, Malaysia, September 2008.
[32]
Mahassni, S.H.; Al-Reemi, R.M. Apoptosis and necrosis of human breast cancer cells by an aqueous extract of garden cress (Lepidium sativum) seeds. Saudi J. Biol. Sci., 2013, 20(2), 131-139.
[http://dx.doi.org/10.1016/j.sjbs.2012.12.002] [PMID: 23961228]

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy