The cytotoxicity effect of crude aqueous and alcoholic extracts of Juncus rigidus on human lung cancer cell line (A549) in vitro

https://doi.org/10.53730/ijhs.v6nS3.7483

Authors

  • Ali Mohmmed Hussen Al-jubouri Department of Biology, Collge of Education for Pure Sciences. University of Kerbala, Iraq
  • Liqaa H. Saqban Department of Biology, Collge of Education for Pure Sciences. University of Kerbala, Iraq

Keywords:

Juncus rigidus, cytotoxcity, inihibition Rate (IR), A549

Abstract

The current study dealt with the identification on cytotoxicity effective of crude water and alcohol extracts from the  Juncus rigidus on human lung cancer cells A549. The quantitative estimation of the active compounds of the water and alcohol extracts of the Juncus (Phenols - Flavonoids - Alkaloids - Tannins) was calculated The results of the aqueous extract were (8.82,5.91,13.42,16.29) mg/g, respectively. While the results of the crude alcoholic extract of the plant were (7.01,6.06,13.84,16.34) mg/g, respectively. The cytotoxicity effect of the water and alcohol  extracts of the plant  was tested on human lung cancer cells A549 and took six concentrations (200,100,50,25,12.5,6.25)micrograms/millilters for 3 exposing times(72, 48, 24)Hr, which recorded  highest inhibition rate was for the alcoholic extract of the plant at a concentration (200) µg/ml, for an exposure period (72) hours, and for a probability level (0.05) that reached (83.45%), while (IR) of cancer cells obtained from the aqueous extract was recorded (68.96%).

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References

Sekar, P., Ravitchandirane, R., Khanam, S., Muniraj, N., & Cassinadane, A. V. (2022). Novel molecules as the emerging trends in cancer treatment: an update. Medical Oncology, 39(2), 1-24.‏

Ferlay, J., Colombet, M., Soerjomataram, I., Parkin, D. M., Piñeros, M., Znaor, A., & Bray, F. (2021). Cancer statistics for the year 2020: An overview. International Journal of Cancer.‏

El-Shamy, A. I., Abdel-Razek, A. F., & Nassar, M. I. (2015). Phytochemical review of Juncus L. genus (Fam. Juncaceae). Arabian Journal of Chemistry, 8(5), 614-623.

Kúsz, N., Stefkó, D., Barta, A., Kincses, A., Szemerédi, N., Spengler, G., ... & Vasas, A. (2021). Juncaceae Species as Promising Sources of Phenanthrenes: Antiproliferative Compounds from Juncus maritimus Lam. Molecules, 26(4), 999.‏

Paśko P, Tyszka-Czochara M, Trojan S, Bobis-Wozowicz S, Zagrodzki P, Namieśnik J, Haruenkit R, Poovarodom S, Pinsirodom P, Gorinstein S. Glycolytic genes expression, proapoptotic potential in relation to the total content of bioactive compounds in durian fruits. Food Research International. 2019 Nov 1;125:108563.

Broadhurst RB, Jones WT. Analysis of condensed tannins using acidified vanillin. Journal of the Science of Food and Agriculture. 1978 Sep;29(9):788- 94.

Marinova D, Ribarova F, Atanassova M. Total phenolics and total flavonoids in Bulgarian fruits and vegetables. Journal of the university of chemical technology and metallurgy. 2005 Jul;40(3):255-60.

Ajanal M, Gundkalle MB, Nayak SU. Estimation of total alkaloid in Chitrakadivati by UV-Spectrophotometer. Ancient science of life. 2012 Apr;31(4):198.

Abdullah, Sulaiman A., Ahmed Majeed Al-Shammari, and Safaa A. Lateef. Attenuated measles vaccine strain have potent oncolytic activity against Iraqi patient derived breast cancer cell line." Saudi journal of biological sciences 27. (2020): 865-872.

Jabir, M. S., Nayef, U. M., Abdulkadhim, W. K., Taqi, Z. J., Sulaiman, G. M., Sahib, U. I., ... & Su, C. C. (2021). Fe 3 O 4 nanoparticles capped with PEG induce apoptosis in breast cancer AMJ13 cells via mitochondrial damage and reduction of NF-κB translocation. Journal of Inorganic and Organometallic Polymers and Materials, 31(3), 1241-1259.

Tawfik, M. M., Galal, B., Nafie, M. S., El Bous, M. M., & El‐Bana, M. I. (2021). Cytotoxic, apoptotic activities and chemical profiling of dimorphic forms of Egyptian halophyte Cakile maritima scop. Journal of Biomolecular Structure and Dynamics, 1-14.‏

Wei, H., Zhang, F., Wang, J., Zhao, M., Hou, T., & Li, L. (2020). Dehydroeffusol inhibits hypoxia-induced epithelial–mesenchymal transition in non-small cell lung cancer cells through the inactivation of Wnt/β-catenin pathway. Bioscience reports, 40(5), BSR20194284.‏

Bús, C., Tóth, B., Stefkó, D., Hohmann, J., & Vasas, A. (2018). Family Juncaceae: Promising source of biologically active natural phenanthrenes. Phytochemistry Reviews, 17(4), 833-851.‏

Lee, Y. M., Lee, G., Oh, T. I., Kim, B. M., Shim, D. W., Lee, K. H., ... & Lim, J. H. (2016). Inhibition of glutamine utilization sensitizes lung cancer cells to apigenin-induced apoptosis resulting from metabolic and oxidative stress. International journal of oncology, 48(1), 399-408.‏

Stefkó, D., Kúsz, N., Barta, A., Kele, Z., Bakacsy, L., Szepesi, Á., ... & Vasas, A. (2020). Gerardiins A–L and structurally related phenanthrenes from the halophyte plant Juncus gerardii and their cytotoxicity against triple-negative breast cancer cells. Journal of natural products, 83(10), 3058-3068.‏

De Natale, A., Pollio, A., Marco, A. D., Luongo, G., Fabio, G. D., & Zarrell, A. (2022). Phenanthrene Dimers: Promising Source of Biologically Active Molecules. Current Topics in Medicinal Chemistry

Petropoulos, S. A., Karkanis, A., Martins, N., & Ferreira, I. C. (2018). Halophytic herbs of the Mediterranean basin: An alternative approach to health. Food and Chemical Toxicology, 114, 155-169.

Published

18-05-2022

How to Cite

Al-jubouri, A. M. H., & Saqban, L. H. (2022). The cytotoxicity effect of crude aqueous and alcoholic extracts of Juncus rigidus on human lung cancer cell line (A549) in vitro. International Journal of Health Sciences, 6(S3), 6664–6673. https://doi.org/10.53730/ijhs.v6nS3.7483

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Section

Peer Review Articles