CYTOTOXIC ACTIVITY EVALUATION OF ERIOCAULON CINEREUM R.BR. ON HELA AND VERO CELL LINES

Authors

  • PINUS JUMARYATNO Department of Pharmacy, Universitas Islam Indonesia, Yogyakarta, Indonesia.
  • ARDE TOGA NUGRAHA Department of Pharmacy, Universitas Islam Indonesia, Yogyakarta, Indonesia.
  • ADILIA TRI HIDAYATI Department of Pharmacy, Universitas Islam Indonesia, Yogyakarta, Indonesia.
  • BAIQ RISKY WAHYU LISNASARI Department of Pharmacy, Universitas Islam Indonesia, Yogyakarta, Indonesia.
  • WIDYANUR MAYA DIAHANDARI Department of Pharmacy, Universitas Islam Indonesia, Yogyakarta, Indonesia.
  • NANANG FAKHRUDIN Department of Pharmaceutical Biology, Faculty of Pharmacy, Universitas Gadjah Mada, Yogyakarta, Indonesia.

DOI:

https://doi.org/10.22159/ijap.2019.v11s5.T0059

Keywords:

Cytotoxic, Eriocaulon cinereum, HeLa cell line, Phytochemical screening, Vero cell line

Abstract

Objective: This study aimed to evaluate the cytotoxic activity of the extracts and fractions of Eriocaulon cinereum against HeLa and Vero cell lines,
which represent cervical cancer and normal cells, respectively. In addition, a phytochemical screening was carried out to determine the chemical
constituents in the extracts and the active fractions.
Materials and Methods: The extracts of E. cinereum were obtained by ultrasound-assisted extraction method using n-hexane, ethyl acetate, and
methanol, successively. The active extract was fractionated using vacuum liquid chromatography with dichloromethane followed by ethyl acetate. The
cytotoxic activity was evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay method and was measured using microplate
reader at the wavelength 595 nm. The data were analyzed with PROBIT from SPSS 16 for Windows®. In addition, phytochemical screening was
performed using standard procedures.
Results: The cytotoxic evaluation of the extracts of E. cinereum showed that the ethyl acetate extract was the most active extract against HeLa cell line
with the half maximal inhibitory concentration (IC50) value of 580.07 μg/ml. The dichloromethane and ethyl acetate fractions from the active extract
of E. cinereum exhibited cytotoxic activity against HeLa cell with the IC50 values of 466.61 μg/ml and 267.34 μg/ml, respectively. In addition, the ethyl
acetate fraction showed a low cytotoxic effect against Vero cell line. The phytochemical screening of the ethyl acetate fraction indicated the presence
of terpenoids and alkaloids.
Conclusion: This finding revealed the anticancer potential of E. cinereum and warranted further investigation for the discovery of new anticancer
agents from natural resources for cervical cancer.

Downloads

Download data is not yet available.

References

1. Stewart BW, Wild CP, editors. In: World Cancer Report 2014. Lyon:
International Agency for Research on Cancer; 2014.
2. Kementerian Kesehatan Republik Indonesia. Info Datin: Situasi
Penyakit Kanker. Pusat Data dan Informasi Kementerian Kesehatan
RI; 2015. Available from: http://www.depkes.go.id/folder/view/01/
structure-publikasi-pusdatin-info-datin.html. [Last accessed
on 2017 June 01].
3. Monk BJ, Sill MW, McMeekin DS, Cohn DE, Ramondetta LM,
Boardman CH, et al. Phase III trial of four cisplatin-containing doublet
combinations in stage IVB, recurrent, or persistent cervical carcinoma:
A gynecologic oncology group study. J Clin Oncol 2009;27:4649-55.
4. Katanyoo K, Tangjitgamol S, Chongthanakorn M, Tantivatana T,
Manusirivithaya S, Rongsriyam K, et al. Treatment outcomes of
concurrent weekly carboplatin with radiation therapy in locally
advanced cervical cancer patients. Gynecol Oncol 2011;123:571-6.
5. Li J, Wang LJ, Zhang BZ, Peng YP, Lin ZQ. Neoadjuvant chemotherapy
with paclitaxel plus platinum for invasive cervical cancer in
pregnancy: Two case report and literature review. Arch Gynecol Obstet
2011;284:779-83.
6. Ackermann S, Beckmann MW, Thiel F, Bogenrieder T. Topotecan in
cervical cancer. Int J Gynecol Cancer 2007;17:1215-23.
7. Mutch DG, Bloss JD. Gemcitabine in cervical cancer. Gynecol Oncol
2003;90:S8-15.
8. American Cancer Society. Chemotherapy for Cervical Cancer.
American Cancer Society, Inc.; 2016. Available from: https://www.
cancer.org/cancer/cervical-cancer/treating/chemotherapy.html.
[Last accessed on 2017 June 01].
9. Xu Q, Xie H, Wu P, Wei X. Flavonoids from the capitula of Eriocaulon
australe. Food Chem 2013;139:149-54.
10. Kim SJ, Lee GT, Lee BR, Jeon KS, Rim HK, Bang JH, et al. Anticancer
effect of Eriocaulon sieboldianum through the activation of
caspase-3 in human leukemia cell line, HL-60 cells. Orient Pharm Exp
Med 2009;9:186-91.
11. Fan Y, Lu H, Ma H, Feng F, Hu X, Zhang Q, et al. Bioactive compounds
of eriocaulon sieboldianum blocking proliferation and inducing
apoptosis of hepG2 cells might be involved in aurora kinase inhibition.
Food Funct 2015;6:3746-59.
12. Fan Y, Lu H, An L, Wang C, Zhou Z, Feng F, et al. Effect of active
fraction of eriocaulon sieboldianum on human leukemia K562 cells
via proliferation inhibition, cell cycle arrest and apoptosis induction.
Environ Toxicol Pharmacol 2016;43:13-20.
13. Nugraha AT, Ramadhan V, Pandapotan H, Romadhonsyah F. A study of
proliferative activity of herbs Eriocaulon cinereum R. Br. on cervical
cancer cells (HeLa) with MTT assay method. Int J Pharm Med Biol Sci
2017;6:73-6.
14. Mandal SC, Mandal V, Das AK. Essential of Botanical Extraction:
Principles and Application. London: Academic Press; 2015.
15. Jones WP, Kinghorn DA. Extraction of plant secondary metabolites. In:
Sarker SD, Latif Z, Gray AI, editors. Natural Products Isolation. 2nd ed.
New Jersey: Humana Press Inc.; 2006. p. 323-51.
16. Jork H, Funk W, Fishcer W, Wimmer H. Thin layer chromatography:
reagents and detection methods. Weinheim: VCH; 1990. Physical and
Chemical Detection Methods, Vol. 1a. J Chromatogr 1993;635:176.
17. Harborne JB. Phytochemical Methods: A Guide to Modern Techniques
of Plant Analysis. 3rd ed. London: Chapman and Hall; 1998.
18. Oliveira ALR, Bove, CP. Eriocaulon L. From Brazil: An annotated
checklist and taxonomic novelties. Acta Bot Bras 2015;29:175-89.
19. Qiao X, Ye G, Liu CF, Zhang ZX, Tu Q, Dong J, et al. Chemical
analysis of eriocaulon buergerianum and adulterating species by highperformance
liquid chromatography with diode array detection and
electrospray ionization tandem mass spectrometry. J Pharm Biomed
Anal 2012;57:133-42.
20. Mahata S, Bharti AC, Shukla S, Tyagi A, Husain SA, Das BC, et al.
Berberine modulates AP-1 activity to suppress HPV transcription and
downstream signaling to induce growth arrest and apoptosis in cervical
cancer cells. Mol Cancer 2011;10:39.
21. Nair JJ, Rárová L, Strnad M, Bastida J, Cheesman L, van Staden J, et al.
Crinane alkaloids of the Amaryllidaceae with cytotoxic effects in human
cervical adenocarcinoma (HeLa) cells. Nat Prod Commun 2014;9:461-6.
22. Li M, Su BS, Chang LH, Gao Q, Chen KL, An P, et al. Oxymatrine
induces apoptosis in human cervical cancer cells through guanine
nucleotide depletion. Anticancer Drugs 2014;25:161-73.
23. Momtaz S, Hussein AA, Ostad SN, Abdollahi M, Lall N. Growth
inhibition and induction of apoptosis in human cancerous HeLa cells
by Maytenus procumbens. Food Chem Toxicol 2013;51:38-45.
24. Huang J, Han HY, Li GY, Wang HY, Zhang C, Zhang K, et al. Two new
terpenoid benzoates with antitumor activity from the roots of Ferula
dissecta. J Asian Nat Prod Res 2013;15:1100-6.
25. Xu X, Yuan J, Zhou X, Li W, Zhu N, Wu H, et al. Cassane diterpenes
with oxygen bridge from the seeds of Caesalpinia sappan. Fitoterapia
2016;112:205-10.

Published

15-09-2019

How to Cite

JUMARYATNO, P., NUGRAHA, A. T., HIDAYATI, A. T., LISNASARI, B. R. W., DIAHANDARI, W. M., & FAKHRUDIN, N. (2019). CYTOTOXIC ACTIVITY EVALUATION OF ERIOCAULON CINEREUM R.BR. ON HELA AND VERO CELL LINES. International Journal of Applied Pharmaceutics, 11(5), 90–93. https://doi.org/10.22159/ijap.2019.v11s5.T0059

Issue

Section

Original Article(s)

Most read articles by the same author(s)

Similar Articles

You may also start an advanced similarity search for this article.