Effects of Vetiveria zizanioides on Cytotoxicity of Human Epithelial Cervical Cancer Cells

S. Si Fadhillah, Amanda Qurrotha Aini, Mualifah, Saifudin, Anom Bowolaksono, Astari Dwiranti

Abstract

The potential of Vetiveria zizanioides or Chrizopogon zizanioides, known as "akar wangi" in Indonesia, has not been much studied as an anticancer ingredient. Moreover, the effect of vetiver compounds on cervical cancer cells is still unknown. This research was conducted to determine the effect of V. zizanioides or vetiver oil on the cytotoxicity of HeLa cells (continuous cell line from cervical cancer epithelial cells) for a further finding of the potential anticancer natural compound. The administration of V. zizanioides extract in essential oil was done in dose-dependent. The 3‑(4,5‑Dimethylthiazolyl‑2‑yl)-2,5-diphenyltetrazolium bromide (MTT) assay as cytotoxicity assay was used to analyze the cytotoxicity effects of vetiver oil for 24 hours to in vitro culture of HeLa cells by determining the percentage of proliferation inhibition. The in vitro HeLa cell culture was treated with several dilutions of vetiver oil. IC50 concentration of 0.02% to 0.00125% vetiver oil against HeLa cells was recorded. The vetiver oil showed cytotoxicity effects against the HeLa cells for 24 hours in a concentration-dependent manner. The highest concentration of vetiver oil (0.02%) showed the highest cell proliferation inhibition (96.304%). The IC50 value was at 0.05% dilution of vetiver oil. In addition, morphological alterations, including cytoplasm shrinkage. Together these findings indicated the active potential anticancer nature of V. zizanioides, especially in human cervical cancer.

 

Keywords: anticancer, cytotoxicity, HeLa cells, vetiver oil, Vetiveria zizanioides.

Full Text:

PDF


References


CATALAN INSTITUTE OF ONCOLOGY AND THE INTERNATIONAL AGENCY FOR RESEARCH ON CANCER. Human Papillomavirus and Related Diseases Report. HPV Information Centre, Barcelona, 2019.

THE GLOBAL CANCER OBSERVATORY. Indonesia’s Cancer Cases. 2019. https://gco.iarc.fr

NEWMAN D. J., CRAGG G. M., and SNADER K. M. J. Natural products as sources of new drugs over the period 1981-2002. Journal of Natural Products, 2003, 66: 1022-1037. https://doi.org/10.1021/np030096l

VINOGRADOV S., & WEI X. Cancer stem cells and drug resistance: the potential of nanomedicine. Nanomedicine, 2012, 7: 597-615. https://doi.org/10.2217/nnm.12.22

CARDENAS M. E., SANDFRIDSON A., CUTER N. S., and HEITMAN J. Traditional medicinal plants as therapeutic agents. Trends in Biotechnology, 1998, 16: 427-433.

LUQMAN S., KUMAR R., KAUSHIK S., SRIVASTAVA S., DAROKAR M. P., and KHANUJA S. P. S. Antioxidant potential of the root of Vetiveria zizanioides (L.) Nash. Indian Journal of Biochemistry and Biophysics, 2009, 46(1): 122-125. https://pubmed.ncbi.nlm.nih.gov/19374265/

LUQMAN S., SRIVASTAVA S., DAROKAR M. P., and KHANUJA P. S. Detection of Antibacterial Activity in Spent Roots of Two Genotypes of Aromatic Grass Vetiveria zizanioides. Pharmaceutical Biology, 2005, 43(8): 732–736. https://doi.org/10.1080/13880200500387471

BALASANKAR D., VANILARASU K., PREETHA P. S., UMADEVI R. M., and BHOWMIK D. Senna - a medical miracle plant. Journal of Medicinal Plants Studies, 2013, 1(3): 191-200. https://www.plantsjournal.com/archives/2013/vol1issue3/PartA/5.pdf

DEVPRAKASH D., SINGH P., SRINIVASAN K. K., SUBBURAJU T., and SINGH S. K. Antifungal activity of alcoholic and aqueous extracts of Vetiveria zizanioides. Journal of Pharmaceutical Research and Opinion, 2011, 1: 85-88. https://www.researchgate.net/publication/221984017_ANTIFUNGAL_ACTIVITY_OF_ALCOHOLIC_AND_AQUEOUS_EXTRACTS_OF_VETIVERIA_ZIZANIOIDES

CHITRA T., JAYASHREE S., and RATHINAMALA J. Evaluation of anticancer activity of Vetiveria zizanioides againsthuman breast cancer cell line. International Journal of Pharmacy and Pharmaceutical Sciences, 2014, 6: 164-166. https://www.researchgate.net/publication/288568667_Evaluation_of_anticancer_activity_of_Vetiveria_Zizanioides_against_human_breast_cancer_cell_line

CHAHAL K. K., BHARDWAJ U., KAUSHAL S., and SANDHU A. K. Chemical composition and biological properties of Chrysopogon zizanioides (L.) Roberty syn. Vetiveria zizanioides (L.) Nash- A Review. Indian Journal of Natural Products and Resources, 2015, 6: 251-260. https://www.researchgate.net/publication/292161359_Chemical_composition_and_biological_properties_of_Chrysopogon_zizanioides_LRoberty_syn_Vetiveria_zizanioides_L_Nash-a_review

SHOAIB M., SHAH I., ALI N., ADHIKARI A., TAHIR M. N., and SHAH S. W. A. Sesquiterpene lactone! a promising antioxidant, anticancer and moderate antinociceptive agent from Artemisia macrocephala jacquem. BMC Complementary Medicine and Therapies, 2017, 17: 27. https://doi.org/10.1186/s12906-016-1517-y

MEHMOOD T., MARYAM A., GHRAMH H. A., KHAN M., and MA T. Deoxyelephantopin and Isodeoxyelephantopin as Potential Anticancer Agents with Effects on Multiple Signaling Pathways. Molecules, 2017, 22: 1013. https://dx.doi.org/10.3390/molecules22061013

AUNG T. N., QU Z., KORTSCHAK R. D., and ADELSON D. L. Understanding the effectiveness of natural compound mixtures in cancer through their molecular mode of action. International journal of molecular sciences, 2017, 18(3): 656. https://doi.org/10.3390/ijms18030656

DOOLEY W. C., ROBERTS J. R., and ALLISON D. C. Acid Giemsa for rapid identification of mitotic cells. Journal of Histochemistry and Cytochemistry, 1989, 37(10): 1553-1556. http://dx.doi.org/10.1177/37.10.2778310

ZACHARY J. F. Pathologic Basis of Veterinary Disease. Elsevier, St. Louis, 2017. https://www.elsevier.com/books/pathologic-basis-of-veterinary-disease-expert-consult/zachary/978-0-323-35775-3

KWON H. K., LEE J. H., SHIN H. J., KIM J. H., and CHOI. S. Structural and functional analysis of cell adhesion and nuclear envelope nano-topography in cell death. Scientific Reports, 2015, 5: 15623. https://doi.org/10.1038/srep15623

CHIU K. K., YE Z. H., and WONG M. H. Growth of Vetiveriazizanioides and Phragmitiesaustralis on Pb/Zn and Cu mine tailings amended with manure compost and sewage sludge: a greenhouse study. Bioresource Technology, 2006, 97(1): 158-170. https://doi.org/10.1016/j.biortech.2005.01.038

LOCK R. B., GALPERINA O. V., FELDHOFF R. C., and RHODES L. J. Concentration-dependent differences in the mechanisms by which caffeine potentiates etoposide cytotoxicity in HeLa cells. Cancer Research, 1994, 54(18): 4933-4939. https://pubmed.ncbi.nlm.nih.gov/8069859/

DEL GIUDICE L., MASSARDO D. R., PONTIERI P., BERTEA C. M., MOMBELLO D., CARATA E., TREDICI S. M., TALÀ A., MUCCIARELLI M., GROUDEVA V. I., DE STEFANO M., VIGLIOTTA G., MAFFEI M. E., and ALIFANO P. Environmental Microbiology, 2008, 10: 2824-2841. https://doi.org/10.1111/j.1462-2920.2008.01703.x

MIRAKABADI A. Z., SHAHRAMYAR Z., MOROVVATI H., LOTFI M., and NOURI A. Induction of apoptosis in human Leukemia cell line (HL60) by Animal’s venom derived peptides (ICD-85). Iranian Journal of Pharmaceutical Research, 2012, 11: 931-938. https://pubmed.ncbi.nlm.nih.gov/24250521/


Refbacks

  • There are currently no refbacks.