PHARMACOLOGICAL INVESTIGATION IN ANTICANCER AND ANTIOXIDANT PROPERTY OF CHRYSANTHEMUM MORIFOLIUM RAMAT.

Main Article Content

Maliha Munawar
Sana Javaid Awan
Alina Farooq
Mubeen Shahzadi
Bushra Adeel
Haleema Usman Khan

Keywords

Chrysanthemum morifolium Ramat, angiogenesis, medicinal plants, anticancer and anti-oxidants

Abstract

Chrysanthemum morifolium Ramat., commonly referred to as the decorative chrysanthemum or simply mum, has served ornamental and therapeutic objectives historically. Traditionally employed to assuage inflammation, fever, and hypertension, modern exploration has paid particular focus to its conceivable function as an antineoplastic and antioxidant ingredient. Its bioactive mixtures, incorporating flavonoids and polyphenols, have proven potential in discouraging malignant cell proliferation, stimulating apoptosis, and bettering antioxidant safeguards.Various tactics were utilized in the research to investigate CM's pharmacological impacts. Plant extracts were ready using methanol, and their cytotoxicity was evaluated using cell viability assays (MTT, Crystal Violet, Trypan Blue). IC50 values were calculated for HeLa and HepG2 cancerous cell lines. Moreover, antioxidant properties were assessed using catalase (CAT), ascorbate peroxidase (APOX), and glutathione reductase (GSH) assays. Enzyme-linked immunosorbent assays (ELISA) measured fluctuations in p53 and VEGF levels. CM revealed dose-dependently cytotoxic impacts against HeLa and HepG2 cells, with notably reductions in cell viability and heightened cell death seen at elevated concentrations. IC50 values indicated powerful antineoplastic action while sparing noncancerous 3T3 cells. Antioxidant assays uncovered enhanced CAT, APOX, and GSH activities in cancerous cells treated with CM, proposing a role in oxidative stress supervision.Chrysanthemum morifolium Ramat. puts forth encouraging anticancer properties through selective cytotoxicity and apoptotic induction in cancerous cells, backed by heightened antioxidant defenses. Its safety profile in normal cells emphasizes its potential as a therapeutic agent with diminished side effects. However, further exploration is necessary to elucidate the underlying molecular mechanisms and validate its efficacy in animal models and clinical trials. These discoveries underscore CM as a candidate for developing targeted cancer therapies and enhancing overall human health.

Abstract 183 | PDF Downloads 63

References

1. Amin, H., Khan, A., Makeen, H. A., Rashid, H., Amin, I., Masoodi, M. H., . . . Rehman, M. U. (2021). Nanosized delivery systems for plant-derived therapeutic compounds and their synthetic derivative for cancer therapy Phytomedicine (pp. 655-675): Elsevier.
2. Borgo, J., Laurella, L. C., Martini, F., Catalán, C. A., & Sülsen, V. P. (2021). Stevia genus: phytochemistry and biological activities update. Molecules, 26(9), 2733.
3. Compton, C., & Compton, C. (2020). A Short History of Cancer: How Did We Get Here? Cancer: The Enemy from Within: A Comprehensive Textbook of Cancer’s Causes, Complexities and Consequences, 83-107.
4. Current, J. R. (2020). How Can We Stop Cancer? The Review: A Journal of Undergraduate Student Research, 21(1), 5.
5. Damasco, J. A., Ravi, S., Perez, J. D., Hagaman, D. E., & Melancon, M. P. (2020). Understanding nanoparticle toxicity to direct a safe-by-design approach in cancer nanomedicine. Nanomaterials, 10(11), 2186.
6. Dehelean, C. A., Marcovici, I., Soica, C., Mioc, M., Coricovac, D., Iurciuc, S., . . . Pinzaru, I. (2021). Plant-derived anticancer compounds as new perspectives in drug discovery and alternative therapy. Molecules, 26(4), 1109.
7. Doan, T. T. M., Tran, G. H., Nguyen, T. K., Kang, K. S., Lim, J. H., & Lee, S. (2024). Comparative Antioxidant Potentials and Quantitative Phenolic Compounds Profiles among the Flowers and Leaves from Various Chrysanthemum morifolium Cultivars. Pharmaceuticals, 17(3), 340.
8. Gabr, S. A., Elsaed, W. M., Eladl, M. A., El-Sherbiny, M., Ebrahim, H. A., Asseri, S. M., . . . Eldesoqui, M. (2022). Curcumin modulates oxidative stress, fibrosis, and apoptosis in drug-resistant cancer cell lines. Life, 12(9), 1427.
9. Garcia-Oliveira, P., Otero, P., Pereira, A. G., Chamorro, F., Carpena, M., Echave, J., . . . Prieto, M. A. (2021). Status and challenges of plant-anticancer compounds in cancer treatment. Pharmaceuticals, 14(2), 157.
10. Hadizadeh, H., Samiei, L., & Shakeri, A. (2022). Chrysanthemum, an ornamental genus with considerable medicinal value: A comprehensive review. South African Journal of Botany, 144, 23-43.
11. Hodaei, M., Rahimmalek, M., & Arzani, A. (2021). Variation in bioactive compounds, antioxidant and antibacterial activity of Iranian Chrysanthemum morifolium cultivars and determination of major polyphenolic compounds based on HPLC analysis. Journal of Food Science and Technology, 58, 1538-1548.
12. Hodaei, M., Rahimmalek, M., & Behbahani, M. (2021). Anticancer drug discovery from Iranian Chrysanthemum cultivars through system pharmacology exploration and experimental validation. Scientific Reports, 11(1), 11767.
13. Khan, A., Choudhury, M., Khanal, S., & Maukeeb, A. (2021). Chrysanthemum indicum, sometimes called mums or chrysanths [1] is one of the most im-portant marketable ornamental and flower plants [2] belonging to the family Compositae/Asteraceae, sub-family Asteroideae, order Asterales, sub-class. Journal of Multidisciplinary Applied Natural Science Vol, 1(1).
14. Khan, A. U., Choudhury, M. A. R., Khan, A. U., Khanal, S., & Maukeeb, A. R. M. (2020). Chrysanthemum production in bangladesh: significance the insect pests and diseases management: A review. Journal of Multidisciplinary Applied Natural Science.
15. Kim, C., Kim, M. C., Kim, S. M., Nam, D., Choi, S. H., Kim, S. H., . . . Ahn, K. S. (2013). Chrysanthemum indicum L. extract induces apoptosis through suppression of constitutive STAT3 activation in human prostate cancer DU145 cells. Phytotherapy Research, 27(1), 30-38.
16. Kim, K.-Y., Oh, T.-W., Yang, H.-J., Kim, Y.-W., Ma, J.-Y., & Park, K.-I. (2019). Ethanol extract of Chrysanthemum zawadskii Herbich induces autophagy and apoptosis in mouse colon cancer cells through the regulation of reactive oxygen species. BMC complementary and alternative medicine, 19, 1-10.
17. Liu, Y., Lu, C., Zhou, J., Zhou, F., Gui, A., Chu, H., & Shao, Q. (2024). Chrysanthemum morifolium as a traditional herb: A review of historical development, classification, phytochemistry, pharmacology and application. Journal of Ethnopharmacology, 118198.
18. Maddala, V. K. S. (2021). Chrysanthemum traditional medicine and its role in biosorption. Annals of the Romanian Society for Cell Biology, 20256-20263.
19. Mohamad, N. V., & Zahari, C. N. M. C. (2024). Biological activities of Chrysanthemum morifolium and Chrysanthemum indicum: Molecular prospective. Journal of Applied Pharmaceutical Science.
20. Ng, T. L., Loh, K. E., Tan, S.-A. S. W., Tan, H. Y., & Wee, S. P. (2020). In vitro and in vivo inhibition of xanthine oxidase by the flowers of Chrysanthemum morifolium Ramat.
21. Ojha, S., Vishwakarma, P. K., Tripathi, S. M., & Mishra, S. (2024). Exploring the Therapeutic Potential of Chrysanthemum morifolium: An Ethnopharmacological Perspective. Current Nutrition & Food Science, 20(5), 646-657.
22. Shamim, S., & Rehman, A. (2015). Antioxidative enzyme profiling and biosorption ability of Cupriavidus metallidurans CH34 and Pseudomonas putida mt2 under cadmium stress. Journal of basic microbiology, 55(3), 374-381.
23. Singh, A., Singh, D. K., Kharwar, R. N., White, J. F., & Gond, S. K. (2021). Fungal endophytes as efficient sources of plant-derived bioactive compounds and their prospective applications in natural product drug discovery: Insights, avenues, and challenges. Microorganisms, 9(1), 197.
24. Wageesha, N. D. A., Soysa, P., Atthanayake, K., Choudhary, M. I., & Ekanayake, M. (2017). A traditional poly herbal medicine “Le Pana Guliya” induces apoptosis in HepG 2 and HeLa cells but not in CC1 cells: an in vitro assessment. Chemistry Central Journal, 11, 1-12.
25. Xue, Y., Wang, J., Huang, Y., Gao, X., Kong, L., Zhang, T., & Tang, M. (2018). Comparative cytotoxicity and apoptotic pathways induced by nanosilver in human liver HepG2 and L02 cells. Human & Experimental Toxicology, 37(12), 1293-1309.
26. Yuan, H., Jiang, S., Liu, Y., Daniyal, M., Jian, Y., Peng, C., . . . Wang, W. (2020). The flower head of Chrysanthemum morifolium Ramat.(Juhua): A paradigm of flowers serving as Chinese dietary herbal medicine. Journal of Ethnopharmacology, 261, 113043.
27. Zhang, J., Wu, Y., Li, Y., Li, S., Liu, J., Yang, X., . . . Wang, G. (2024). Natural products and derivatives for breast cancer treatment: From drug discovery to molecular mechanism. Phytomedicine, 155600.