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Received: 2023-10-17

Revision Accepted: 2024-05-08

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Journal of Zhejiang University SCIENCE B 2014 Vol.15 No.8 P.692-700

http://doi.org/10.1631/jzus.B1300303


Piper betle leaf extract enhances the cytotoxicity effect of 5-fluorouracil in inhibiting the growth of HT29 and HCT116 colon cancer cells*


Author(s):  Pek Leng Ng1, Nor Fadilah Rajab1, Sue Mian Then2,3, Yasmin Anum Mohd Yusof4, Wan Zurinah Wan Ngah2,4, Kar Yong Pin5, Mee Lee Looi6

Affiliation(s):  1. Department of Biomedical Sciences, Faculty of Allied Health, Universiti Kebangsaan Malaysia (UKM), Jalan Raja Muda Abdul Aziz, 50300 Kuala Lumpur, Malaysia; more

Corresponding email(s):   MeeLee.Looi@taylors.edu.my

Key Words:  Piperaceae , Piper betle L., 5-Fluorouracil, Isobologram analysis, Herb-drug interaction


Pek Leng Ng, Nor Fadilah Rajab, Sue Mian Then, Yasmin Anum Mohd Yusof, Wan Zurinah Wan Ngah, Kar Yong Pin, Mee Lee Looi. Piper betle leaf extract enhances the cytotoxicity effect of 5-fluorouracil in inhibiting the growth of HT29 and HCT116 colon cancer cells[J]. Journal of Zhejiang University Science B, 2014, 15(8): 692-700.

@article{title="Piper betle leaf extract enhances the cytotoxicity effect of 5-fluorouracil in inhibiting the growth of HT29 and HCT116 colon cancer cells",
author="Pek Leng Ng, Nor Fadilah Rajab, Sue Mian Then, Yasmin Anum Mohd Yusof, Wan Zurinah Wan Ngah, Kar Yong Pin, Mee Lee Looi",
journal="Journal of Zhejiang University Science B",
volume="15",
number="8",
pages="692-700",
year="2014",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B1300303"
}

%0 Journal Article
%T Piper betle leaf extract enhances the cytotoxicity effect of 5-fluorouracil in inhibiting the growth of HT29 and HCT116 colon cancer cells
%A Pek Leng Ng
%A Nor Fadilah Rajab
%A Sue Mian Then
%A Yasmin Anum Mohd Yusof
%A Wan Zurinah Wan Ngah
%A Kar Yong Pin
%A Mee Lee Looi
%J Journal of Zhejiang University SCIENCE B
%V 15
%N 8
%P 692-700
%@ 1673-1581
%D 2014
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B1300303

TY - JOUR
T1 - Piper betle leaf extract enhances the cytotoxicity effect of 5-fluorouracil in inhibiting the growth of HT29 and HCT116 colon cancer cells
A1 - Pek Leng Ng
A1 - Nor Fadilah Rajab
A1 - Sue Mian Then
A1 - Yasmin Anum Mohd Yusof
A1 - Wan Zurinah Wan Ngah
A1 - Kar Yong Pin
A1 - Mee Lee Looi
J0 - Journal of Zhejiang University Science B
VL - 15
IS - 8
SP - 692
EP - 700
%@ 1673-1581
Y1 - 2014
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B1300303


Abstract: 
Objective: The combination effect of Piper betle (PB) and 5-Fluorouracil (5-FU) in enhancing the cytotoxic potential of 5-FU in inhibiting the growth of colon cancer cells was investigated. Methods: HT29 and HCT116 cells were subjected to 5-FU or PB treatment. 5-FU and PB were then combined and their effects on both cell lines were observed after 24 h of treatment. PB-5-FU interaction was elucidated by isobologram analysis. Apoptosis features of the treated cells were revealed by annexin V/PI stain. High-performance liquid chromatography (HPLC) was performed to exclude any possible chemical interaction between the compounds. Results: In the presence of PB extract, the cytotoxicity of 5-FU was observed at a lower dose (IC50 12.5 μmol/L) and a shorter time (24 h) in both cell lines. Both cell lines treated with 5-FU or PB alone induced a greater apoptosis effect compared with the combination treatment. isobologram analysis indicated that PB and 5-FU interacted synergistically and antagonistically in inhibiting the growth of HT29 and HCT116 cells, respectively. Conclusions: In the presence of PB, a lower dosage of 5-FU is required to achieve the maximum drug effect in inhibiting the growth of HT29 cells. However, PB did not significantly reduce 5-FU dosage in HCT116 cells. Our result showed that this interaction may not solely contribute to the apoptosis pathway.

蒌叶提取物增强5-氟尿嘧啶对结肠癌细胞HT29和HCT116的生长抑制作用

研究目的:探讨蒌叶(PB)提取物对5-氟尿嘧啶(5-FU)抑制结肠癌细胞HT29和HCT116生长的影响。
研究方法:HT29和HCT116细胞分别给予PB、5-FU以及两种药物联合治疗24小时,应用等效线图法分析PB和5-FU的药效学相互作用,AnnexinV/PI染色法检测HT29和HCT116细胞的凋亡情况,高效液相色谱法排除PB和5-FU间任何可能的相互化学作用。
重要结论:联合PB,低剂量5-FU可以在短时间内起到细胞毒作用,而单独应用PB或5-FU治疗较联合治疗可以诱导更多细胞发生凋亡。进一步采用等效线图法分析显示PB和5-FU的联合作用在抑制结肠癌细胞HT29和HCT116的生长中分别体现出协同和拮抗作用。因此可以认为在HT29细胞中,PB使得较低剂量5-FU发挥最大抑制结肠癌细胞生长效果,然而在HCT116细胞中,PB没有显著降低5-FU的药物浓度,说明PB和5-FU的相互作用不仅仅体现在诱导细胞凋亡方面。
胡椒科;蒌叶;5-氟尿嘧啶;等效线图法;草药-药物相互作用

Darkslateblue:Affiliate; Royal Blue:Author; Turquoise:Article

References

[1] Ahmad, M., Usman, M., Madni, A., 2011. A fast and simple HPLC-UV method for simultaneous determination of three anti-cancer agents in plasma of breast cancer patients and its application to clinical pharmacokinetics. Afr J Pharm Pharmacol, 5(7):915-922. 

[2] Arambewela, L., Arawwawala, M., Rajapaksa, D., 2006.  Piper betle: a potential natural antioxidant. Int J Food Sci Technol, 41(s1):10-14. 


[3] Boyer, J., McLean, E.G., Aroori, S., 2004. Characterization of p53 wild-type and null isogenic colorectal cancer cell lines resistant to 5-fluorouracil, oxaliplatin, and irinotecan. Clin Cancer Res, 10(6):2158-2167. 


[4] Bunz, F., Hwang, P.M., Torrance, C., 1999. Disruption of p53 in human cancer cells alters the responses to therapeutic agents. J Clin Invest, 104(3):263-269. 


[5] Cabrera, J., Mancuso, M., Cabrera-Franquiz, F., 2011. Stability and compatibility of the mixture of tramadol, ketorolac, metoclopramide and ranitidine in a solution for intravenous perfusion. Farm Hosp, (in Spanish),35(2):80-83. 


[6] Chakraborty, J.B., Mahato, S.K., Joshi, K., 2012. Hydroxychavicol, a Piper betle leaf component, induces apoptosis of CML cells through mitochondrial reactive oxygen species-dependent JNK and endothelial nitric oxide synthase activation and overrides imatinib resistance. Cancer Sci, 103(1):88-99. 


[7] Chang, M., Uang, B., Wu, H.L., 2002. Inducing the cell cycle arrest and apoptosis of oral KB carcinoma cells by hydroxychavicol: roles of glutathione and reactive oxygen species. Brit J Pharmacol, 135(3):619-630. 


[8] Chou, T.C., 2006. Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies. Pharmacol Rev, 58(3):621-681. 


[9] Esimone, C.O., 2011. Drug-drug and herb-drug interaction—a comment. J Res Nat Dev, 9(1):47-59. 

[10] Fathilah, A.R., Sujata, R., Norhanom, A.W., 2010. Antiproliferative activity of aqueous extract of Piper betle L. and Psidium guajava L. on KB and HeLa cell lines. J Med Plants Res, 4(11):987-990. 

[11] Felth, J., Rickardson, L., Rosen, J., 2009. Cytotoxic effects of cardiac glycosides in colon cancer cells, alone and in combination with standard chemotherapeutic drugs. J Nat Prod, 72(11):1969-1974. 


[12] Fishbein, A.B., Wang, C.Z., Li, X.L., 2009. Asian ginseng enhances the anti-proliferative effect of 5-fluorouracil on human colorectal cancer: comparison between white and red ginseng. Arch Pharm Res, 32(4):505-513. 


[13] Guha, P., 2006. Betel leaf: the neglected green gold of India. J Hum Ecol, 19(2):87-93. 

[14] Hemamalini, V., Dass Prakash, M.V., Sivaramakrishnan, S., 2012. Evaluation of the in vitro antioxidant, anti-enteropathogenic and anticancer efficacy of natural and synthetic hydroxychavicol. Int J Medicobiol Res, 1(5):250-254. 

[15] Hiss, D.C., Gabriels, G.A., Folb, P.I., 2007. Combination of tunicamycin with anticancer drugs synergistically enhances their toxicity in multidrug-resistant human ovarian cystadenocarcinoma cells. Cancer Cell Int, 7(1):5


[16] Hrmann, V., Kumi-Diaka, J., Durity, M., 2012. Anticancer activities of genistein-topotecan combination in prostate cancer cells. J Cell Mol Med, 16(11):2631-2636. 


[17] Hussin, A.H., 2001. Adverse effects of herbs and drug-herbal interactions. Malays J Pharm, 1(2):39-44. 

[18] Jeng, J., Chen, S., Liao, C., 2002. Modulation of platelet aggregation by areca nut and betel leaf ingredients: roles of reactive oxygen species and cyclooxygenase. Free Radic Biol Med, 32(9):860-871. 


[19] Jeng, J.H., Wang, Y.J., Chang, W.H., 2004. Reactive oxygen species are crucial for hydroxychavicol toxicity toward KB epithelial cells. Cell Mol Life Sci, 61(1):83-96. 


[20] Jin, J., Huang, M., Wei, H.L., 2002. Mechanism of 5-fluorouracil required resistance in human hepatocellular carcinoma cell line Bel7402World J Gastroenterol, 8(6):1029-1034. 


[21] Kinsella, A., Smith, D., Pickard, M., 1997. Resistance to chemotherapeutic antimetabolites: a function of salvage pathway involvement and cellular response to DNA damage. Brit J Cancer, 75(7):935-945. 


[22] Klampfer, L., Swaby, L.A., Huang, J., 2005. Oncogenic Ras increases sensitivity of colon cancer cells to 5-FU-induced apoptosis. Oncogene, 24(24):3932-3941. 


[23] Kumar, N., Misra, P., Dube, A., 2010.  Piper betle Linn. a maligned Pan-asiatic plant with an array of pharmacological activities and prospects for drug discovery. Curr Sci, 99(7):922-932. 

[24] Kumar, S., Choudhary, S., Singh, N., 2012. Combination of natural drugs: an emerging trend in cancer chemotherapy. J Drug Deliv Ther, 2(3):97-105. 

[25] Mader, R.M., Mller, M., Steger, G.G., 1998. Resistance to 5-fluorouracil. Gen Pharmacol, 31(5):661-666. 


[26] Majumdar, A.P., Banerjee, S., Nautiyal, J., 2009. Curcumin synergizes with resveratrol to inhibit colon cancer. Nutr Cancer, 61(4):544-553. 


[27] Molyneux, P., 2004. The use of the stable free radical diphenylpicrylhydrazyl (DPPH) for estimating antioxidant activity. Songklanakarin J Sci Technol, 26(2):211-219. 

[28] Nakagawa, Y., Suzuki, T., Nakajima, K., 2009. Biotransformation and cytotoxic effects of hydroxychavicol, an intermediate of safrole metabolism, in isolated rat hepatocytes. Chem Biol Interact, 180(1):89-97. 


[29] Newton, D.W., 2009. Drug incompatibility chemistry. Am J Health Syst Pharm, 66(4):348-357. 


[30] Noordhuis, P., Holwerda, U., van der Wilt, C., 2004. 5-Fluorouracil incorporation into RNA and DNA in relation to thymidylate synthase inhibition of human colorectal cancers. Ann Oncol, 15(7):1025-1032. 


[31] Pin, K., Chuah, A.L., Rashid, A.A., 2010. Antioxidant and anti-inflammatory activities of extracts of betel leaves (Piper betle) from solvents with different polarities. J Trop For Sci, 22(4):448-455. 

[32] Pin, K.Y., Ilicali, C., Luqman Chuah, A., 2011. Modelling of freezing kinetics of extract of betel leaves (Piper betle L.). Int J Food Eng, 7(1):Art. 15


[33] Pizzorno, G., Diasio, R.B., Cheng, Y.C., 2009.  Cancer Medicine. Peoples Medical Publishing House-USE,USA :

[34] Pourcel, L., Routaboul, J.M., Cheynier, V., 2007. Flavonoid oxidation in plants: from biochemical properties to physiological function. Trends Plant Sci, 12(1):29-36. 


[35] Renuka, G., Thiruvengadarajan, V.S., Amruthkumar, N., 2011. A review on herb-drug interactions. Int J Pharm Res Dev, 3(3):136-153. 

[36] Slovin, S., 2012. Chemotherapy and immunotherapy combination in advanced prostate cancer. Clin Adv Hematol Oncol, 10(2):90-100. 


[37] Tallarida, R.J., Raffa, R.B., 1996. Testing for synergism over a range of fixed ratio drug combinations: replacing the isobologram. Life Sci, 58(2):23-28. 


[38] Tang, X.Y., Zhu, Y.Q., Tao, W.H., 2007. Synergistic effect of triptolide combined with 5-fluorouracil on colon carcinoma. Postgrad Med J, 83(979):338-343. 


[39] Tong, J., Xie, G., He, J., 2011. Synergistic antitumor effect of dichloroacetate in combination with 5-fluorouracil in colorectal cancer. J Biomed Biotechnol, 2011:740564


[40] Wang, C.Z., Yuan, C.S., 2008. Potential role of ginseng in the treatment of colorectal cancer. Am J Chin Med, 36(6):1019-1028. 


[41] Yamai, H., Sawada, N., Yoshida, T., 2009. Triterpenes augment the inhibitory effects of anticancer drugs on growth of human esophageal carcinoma cells in vitro and suppress experimental metastasis in vivoInt J Cancer, 125(4):952-960. 


[42] Young, S.C., Wang, C.J., Hsu, J.D., 2006. Increased sensitivity of HepG2 cells toward the cytotoxicity of cisplatin by the treatment of Piper betel leaf extract. Arch Toxicol, 80(6):319-327. 


[43] Zong, W.X., Thompson, C.B., 2006. Necrotic death as a cell fate. Genes Dev, 20(1):1-15. 



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