Skip to main navigation menu Skip to main content Skip to site footer

Research Articles

Vol. 12 No. 3 (2025)

From toxic ornamental to therapeutic prospect: Phytochemical profile and cytotoxic evaluation of n-hexane extract from Iraqi Senecio rowleyanus

DOI
https://doi.org/10.14719/pst.9137
Submitted
27 April 2025
Published
25-07-2025 — Updated on 06-08-2025
Versions

Abstract

Senecio rowleyanus H. Jacobsen plant belongs to Asteraceae family that contain over 1600 genera and approximately 2500 species that have important pharmacological roles in human life. This study assesses the n-hexane extract of Senecio rowleyanus, introduces a new CombiFlash-based method for phytochemical isolation and evaluates its pharmacological effect against breast cancer cells. The whole plant was extracted using maceration in n-hexane and analyzed by Gas Chromatography- Mass Spectrometry (GC-MS). Phytosterols were isolated using CombiFlash column chromatography, yielding several fractions; only fraction B matched lupeol, confirmed by HPLC and FT-IR. Cytotoxicity of the extract was evaluated using the MTT assay on AMJ13 breast cancer cells treated with concentrations (1000, 500, 250, 125, 62.5 and 31.75 µg/mL) for 72 hrs, with doxorubicin as a control. Cell viability was then assessed. GC-MS analysis confirmed the presence of multiple bioactive phytosterols, which revealed a high content of β- and γ-sitosterol (17 %), spathulenol (13 %) and α-amyrin (9 %). with lupeol identified in a specific purified fraction. The n-hexane extract exhibited a cytotoxic effect on AMJ13 cells with an IC₅₀ value of 125.3 μg/mL, showing a concentration- and time-dependent reduction in cell viability. The observed cytotoxicity was notable when compared to the standard drug, doxorubicin. Senecio rowleyanus cultivated in Iraq demonstrates potent anticancer potential, with lupeol and other phytosterols exhibiting significant cytotoxicity against breast cancer cells. These findings support its promise as a natural candidate for pharmaceutical development, further mechanistic and clinical investigations is requiring.

References

  1. 1. Hasan HT, Kadhim EJ. Phytochemical investigation of Corchorus olitorius L. leaves cultivated in Iraq and it’s in vitro antiviral activity. Iraqi Journal of Pharmaceutical Sciences (P-ISSN 1683-3597 E-ISSN 2521-3512). 2018:115-22. https://doi.org/10.31351/vol27iss2pp115-122
  2. 2. Jacobsen H. String-of-beads senecio: Senecio rowleyanus Jacobs nov. spec. The National Cactus and Succulent Journal. 1968;23(2):30-1.
  3. 3. Rolnik A, Olas B. The plants of the Asteraceae family as agents in the protection of human health. Int J Mol Sci. 2021;22(6):3009. https://doi.org/10.3390/ijms22063009
  4. 4. Achika JI, Arthur DE, Gerald I, Adedayo A. A review on the phytoconstituents and related medicinal properties of plants in the Asteraceae family. IOSR J Appl Chem. 2014;7(8):1-8.
  5. 5. Al-Subaie SF, Alowaifeer AM, Mohamed ME. Pyrrolizidine alkaloid extraction and analysis: Recent updates. Foods. 2022;11(23):3873. https://doi.org/10.3390/foods11233873
  6. 6. Ghalib SA, Kadhim EJ. The investigation of some phytochemical compounds found in Anchusa strigosa L. Grown naturally in Iraq. Iraqi Journal of Pharmaceutical Sciences (P-ISSN 1683-3597 E-ISSN 2521-3512). 2021;30(1):179-88. https://doi.org/10.31351/vol30iss1pp179-188
  7. 7. Ashour R. Chemical profile and biological activities of the aerial parts of Senecio acaulis (Lf) Sch Bip. Pharmacognosy Research. 2018;10:2. http:// doi.org/10.4103/pr.pr_149_17
  8. 8. Elsharkawy ER. GC-MS analysis of chemical composition, cytotoxicity and antioxidant activities of essential oils of Senecio glaucus under drastic conditions. Main Group Chemistry. 2022;21(1):233-41. https://doi.org/10.3233/MGC-210125
  9. 9. Ouhaddou S, Aghraz A, Ben Bakrim W, Sissi S, Larhsini M, Markouk M, et al. Analysis of volatiles in Senecio anteuphorbium essential oil with a focus on its allelopathic effect by means of gas chromatography. Separations. 2022;9(2):36. https://doi.org/10.3390/separations9020036
  10. 10. El Hawary S, Galal A, Yousif M, Kirollos F. GC-MS and bioactivity of the essential oil of Senecio rowleyanus Jacobs. Pharmacognosy magazine. 2008;4(16):273.
  11. 11. Yara D, Oroszi T. Understanding breast cancer: A comprehensive review of epidemiology, risk factors and treatment strategies. Advances in Breast Cancer Research. 2025;14(1):1-5. https://doi.org/10.4236/abcr.2025.141001
  12. 12. Boontha, Supavadee et al. Cytotoxic, cell apoptosis, colony formation and anti-migratory activity of three herbal plant extracts in MCF-7 breast cancer cells. Natural and Life Sciences Communications. 2024.
  13. 13. Jenča A, Mills DK, Ghasemi H, Saberian E, Jenča A, Karimi Forood AM, et al. Herbal therapies for cancer treatment: A review of phytotherapeutic efficacy. Biologics: Targets and Therapy. 2024:229-55. https://doi.org/10.2147/BTT.S484068
  14. 14. Mathe E, Sethoga L, Mapfumari S, Adeniran O, Mokgotho P, Shai J, et al. Phytochemical screening and characterization of volatile compounds from three medicinal plants with reported anticancer properties using GC-MS. Life. 2024;14(11):1375. https://doi.org/10.3390/life14111375
  15. 15. Kasprowiak A, Cazier-Dennin F, Danjou PE. Flash chromatography system: A practical tool for demonstrating the influence of column characteristics on chromatographic resolution. Journal of Chemical Education. 2020;97(4):1145-50. https://doi.org/10.1021/acs.jchemed.9b00929
  16. 16. Hussien MS, Al-Hamashi AA. Phytosterol profile in Iraqi Lactuca serriola after purification and isolation by combiflash and HPLC (Conference Paper). Iraqi Journal of Pharmaceutical Sciences (P-ISSN 1683-3597 E-ISSN 2521-3512). 2022;31:54-61. https://doi.org/10.31351/vol31issSuppl.pp54-61
  17. 17. Ismail NR, Kadhim EJ. Phytochemical screening and isolation of new compounds. International Journal of Drug Delivery Technology. 2021;11(3):1033-9.
  18. 18. Krysa M, Szymańska-Chargot M, Zdunek A. FT-IR and FT-Raman fingerprints of flavonoids: A review. Food Chemistry. 2022;393:133430. https://doi.org/10.1016/j.foodchem.2022.133430
  19. 19. Novais Â, Peixe L. Fourier transform infrared spectroscopy (FT-IR) for food and water microbiology. Application and Integration of Omics-powered Diagnostics in Clinical and Public Health Microbiology. 2021:191-217. https://doi.org/10.1007/978-3-030-62155-1_11
  20. 20. Al-Shammari, Ahmed Majeed, Mortadha A Alshami, Mahfoodha Abbas Umran, Asmaa Amer Almukhtar, Nahi Y Yaseen, et al. Establishment and characterization of a receptor-negative, hormone-nonresponsive breast cancer cell line from an Iraqi patient. Breast Cancer: Targets and Therapy. 2015:223-30. https://doi.org/10.2147/bctt.s74509
  21. 21. Salman MI, Emran MA, Al-Shammari AM. Spheroid-formation 3D engineering model assay for in vitro assessment and expansion of cancer cells. InAIP Conference Proceedings. AIP Publishing. 2021;2372(1). https://doi.org/10.1063/5.0065362
  22. 22. Mahmood MA, Abd AH, Kadhim EJ. Assessing the cytotoxicity of phenolic and terpene fractions extracted from Iraqi Prunus arabica on AMJ13 and SK-GT-4 human cancer cell lines. F1000Res. 2023;12:433. https://doi.org/10.12688/f1000research.131336.3
  23. 23. Salman, Marwa Ibrahim, Ahmed Majeed Al-Shammari, Mahfodha Abbas Emran. 3-Dimensional coculture of breast cancer cell lines with adipose tissue - derived stem cells reveal the efficiency of oncolytic Newcastle disease virus infection via labeling technology. Frontiers in Molecular Biosciences. 2022;(9):986. https://doi.org/10.3389/fmolb.2022.754100
  24. 24. Al-Shammari, A M, Salman M I. Antimetastatic and antitumor activities of oncolytic NDV AMHA1 in a 3D culture model of breast cancer. Frontiers in Molecular Biosciences. 2024;(11);1331369. ‏ https://doi.org/10.3389/fmolb.2024.1331369
  25. 25. Mus’hib HK, Abdul-jalil TZ. Lupeol: triterpene from Iraqi Portulaca grandiflora L (Portulacaceae): Its extraction, identification (GC/MS), isolation (Combiflash) and structure elucidation. Iraqi Journal of Pharmaceutical Sciences. 2024;33(4SI)):147-58. https://doi.org/10.31351/vol33iss(4SI)pp147-158
  26. 26. Almeida CA, Baggio SR, Mariutti LR, Bragagnolo N. One-step rapid extraction of phytosterols from vegetable oils. Food Research International. 2020;130:108891. https://doi.org/10.1016/j.foodres.2019.108891
  27. 27. Panal Sitorus PS, Urip Harahap UH, Pandapotan M, Tonel Barus TB. Isolation of β-sitosterol from n-hexane extract of Picria fel-terrae Lour. leave and study of its antidiabetic effect in alloxan induced diabetic mice. Int J Pharm Technol Res. 2014;6:137-41.
  28. 28. Silihe KK, Zingue S, Yeshak MY, Bisrat D, Kemboi D, Bräutigam K, et al. Purification of α-amyrin-acetate and phenylpropanoïd compounds from Ficus umbellata Vahl (Moraceae) stem bark and evaluation of their anti-breast cancer potential. South African Journal of Botany. 2025;177:445-56. https://doi.org/10.1016/j.sajb.2024.12.015
  29. 29. Afzal O, Akhter MH, Ahmad I, Muzammil K, Dawria A, Zeyaullah M, et al. A β–sitosterol encapsulated biocompatible alginate/chitosan polymer nanocomposite for the treatment of breast cancer. Pharmaceutics. 2022;14(8):1711. https://doi.org/10.3390/pharmaceutics14081711
  30. 30. Zhang X, Gao Z, Chen K, Zhuo Q, Chen M, Wang J, et al. Lupeol inhibits the proliferation and migration of MDA-MB-231 breast cancer cells via a novel crosstalk mechanism between autophagy and the EMT. Food & Function. 2022;13(9):4967-76. https://doi.org/10.1039/d2fo00483f

Downloads

Download data is not yet available.