ISOLATION, STRUCTURAL ELUCIDATION, AND ANTICANCER EVALUATION OF BIOACTIVE COMPOUNDS FROM CEIBA SPECIOSA USING CHROMATOGRAPHIC AND SPECTROSCOPIC TECHNIQUES
Keywords:
Ceiba speciosa, anticancer assays, oncology, cytotoxic, cancer cell lines, structurally elucidateAbstract
This study will isolate and structurally characterize bioactive compounds in Ceiba speciosa and determine
the anticancer activity of those substances; the problem to be solved is the identification and
characterization of potentially effective anticancer agents of this plant, which will require the generation
of information on chemical composition via chromatographic techniques and the evaluation of biological
activity in terms of in vitro anticancer assays. The present work will isolate and structurally characterize
as well as determine the possible anticancer activity of bioactive compounds in Ceiba speciosa, a rather
necessary phenomenon because the question concerning the development of effective drugs of natural
anticancer activity is urgent. Diverse chromatographic methods allowed extracting and identifying a
number of compounds, including some that had not been previously described as being bioactive. The
study, which was of interest, found certain compounds that demonstrated great levels of cytotoxic activity
in vitro associated with different types of cancer cell lines, and the results were quite promising in terms
of therapy. These results support the idea of the great role that natural products including products of
Ceiba speciosa may have in obtaining new anticancer drugs. The findings are of key importance to the
structural diversity and biological activity of plant-derived agents, indicating that additional research on
these agents may bring new solutions in the treatment of oncology. The study not only expands the picture
of the pharmacological potential of Ceiba speciosa, but it also underlines the role of the natural products
in the health-care sector, which has become necessary because of increased drug resistance and
secondary effects related to standard therapies. The long-term impact of this research is that plant-based
sources should be exhausted more in the search of new agents to treat cancers which might be effective
yet less toxic.
References
1. Kuna, L., Jakab, J., Smolic, R., Raguz-Lucic, N., Vcev, A., & Smolic, M. (2019). Peptic ulcer disease: A brief review of conventional therapy and herbal treatment options. Journal of Clinical Medicine, 8(2), 179.
2. Lanas, A., & Chan, F. K. L. (2017). Peptic ulcer disease. The Lancet, 390(10094), 613–624.
3. Kim, Y., Park, H. J., Kim, H., Song, J., & Lee, D. (2019). Gastroprotective effects of Paeonia extract mixture HT074 against experimental gastric ulcers in rats. Evidence-Based Complementary and Alternative Medicine, 2019, Article ID 3546258.
4. Yuan, Y., Padol, I. T., & Hunt, R. H. (2006). Peptic ulcer disease today. Nature Clinical Practice Gastroenterology & Hepatology, 3(2), 80–89.
5. Wallace, J. L. (2019). Prostaglandins, NSAIDs, and gastric mucosal protection: Why doesn’t the stomach digest itself? Physiological Reviews, 88(4), 1547–1565.
6. Yang, Y., Kim, S. C., Yu, T., Yi, Y., Rhee, M. H., Sung, G., Yoo, B. C., & Cho, J. Y. (2014). Functional roles of p38 mitogen-activated protein kinase in macrophage-mediated inflammatory responses. Mediators of Inflammation, 2014, Article ID 352371.
7. Mancini, A. D., & Di Battista, J. A. (2011). The cardinal role of the phospholipase A2/cyclooxygenase-2/prostaglandin E synthase/prostaglandin E2 (PCPP) axis in inflammostasis. Inflammation Research, 60(12), 1083–1092.
8. Tamaddonfard, E., Erfanparast, A., Abbas, A., & Imani, M. (2019). Safranal, a constituent of saffron, exerts gastro-protective effects against indomethacin-induced gastric ulcer. Life Sciences, 224, 88–94.
9. Anosike, C. A., & Ofoegbu, R. E. (2013). Anti-ulcerogenic activity of the methanol extract of Ceiba pentandra stem bark on indomethacin and ethanol-induced ulcers in rats. International Journal of Pharmaceutical Sciences, 3(3), 223–228.
10. Newman, D. J., & Cragg, G. M. (2012). Natural products as sources of new drugs over the 30 years from 1981 to 2010. Journal of Natural Products, 75(3), 311–335.
11. Kim, J. I., Park, S. W., Lim, J. J., Sohn, S. I., Shin, J. S., Park, S. C., et al. (2017). Gastroprotective effects of the isopropanol extract of Artemisia princeps and its gastroretentive floating tablets on gastric mucosal injury. Acta Pharmaceutica, 67(4), 479–494.
12. Sen, S., Chakraborty, R., De, B., & Mazumder, J. (2009). Plants and phytochemicals for peptic ulcer: An overview. Pharmacognosy Reviews, 3(6), 270–279.
13. Anosike, C. A., Ugwu, J. C., Ojeli, P. C., & Abugu, S. C. (2014). Anti-ulcerogenic effects and anti-oxidative properties of Ceiba pentandra leaves on alloxan-induced diabetic rats. European Journal of Medicinal Plants, 4(4), 458–472.
14. Dörr, J. A., Bitencourt, S., Bortoluzzi, L., Alves, C., Stoll, S., Pinteus, S., et al. (2018). In vitro activities of Ceiba speciosa (A. St.-Hil) Ravenna aqueous stem bark extract. Natural Product Research, 33(23), 3441–3444.
15. Mohan, A., Sagar, S., Bhanu, P., & Talole, B. (2013). Phytochemical screening, flavonoid content and antioxidant activity of ethanolic extract of Ceiba pentandra. Journal of Ethnopharmacology, 4(2), 240–243.
16. Ladeji, O., Omekarah, I., & Solomon, M. (2003). Hypoglycemic properties of aqueous bark extract of Ceiba pentandra in streptozotocin-induced diabetic rats. Journal of Ethnopharmacology, 84(2–3), 139–142.
17. Bhushan, G., Kavimani, S., & Raj Kapoor, B. (2011). Antiulcer activity of methanolic extract of Ceiba pentandra (Linn.) Gaertn. on rats. Journal of Pharmaceutical Research, 4(12), 4132–4134.
18. Khan, A., Asadsaeed, M., Ahmed Chaudhary, M., Ahmad, Q., & Ansari, F. (2015). Antimicrobial, anti-inflammatory and antipyretic activity of Chorisia speciosa leaves (Bombacaceae). International Journal of Biology, Pharmacy and Allied Sciences, 4(8), 6826–6838.
19. Nasr, E. M., Assaf, M. H., Ramadan, M. A., & Darwish, F. M. (2018). Phytochemical and biological study of Chorisia speciosa A. St. Hil. cultivated in Egypt. Journal of Pharmacognosy and Phytochemistry, 7(1), 649–656.
20. Dörr, J. A. (2018). Avaliação da atividade anti-inflamatória e antiulcerogênica de extratos de Ceiba speciosa (A. St.-Hil) Ravenna em modelos experimentais in vitro e in vivo. [Master’s thesis].
https://oasisbr.ibict.br/vufind
21. Malheiros, C. K. C., Silva, J. S. B., Hofmann, T. C., Messina, T. M., Manfredini, V., Piccoli, J. D. C. E., et al. (2017). Preliminary in vitro assessment of the potential toxicity and antioxidant activity of Ceiba speciosa (A. St.-Hill) Ravenna (paineira). Brazilian Journal of Pharmaceutical Sciences, 53(4), e16106.
22. Refaat, J., Desoky, S. Y., Ramadan, M. A., & Kamel, M. S. (2013). Bombacaceae: A phytochemical review. Pharmaceutical Biology, 51(1), 100–130.
23. Pauli, G. F., Poetsch, F., & Nahrstedt, A. (1998). Structure assignment of natural quinic acid derivatives using proton nuclear magnetic resonance techniques. Phytochemical Analysis, 9(4), 177–185.
24. Flores-Parra, A., Gutiérrez-Avella, D. M., Contreras, R., & Khuong-Huu, F. (1989). 13C and 1H NMR investigations of quinic acid derivatives: Complete spectral assignment and elucidation of preferred conformations. Magnetic Resonance in Chemistry, 27(6), 544–555.
25. Tawaha, K., Alali, F. Q., Gharaibeh, M., Mohammad, M., & El-Elimat, T. (2007). Antioxidant activity and total phenolic content of selected Jordanian plant species. Food Chemistry, 104(4), 1372–1378.
26. Loganayaki, N., Siddhuraju, P., & Manian, S. (2013). Antioxidant activity and free radical scavenging capacity of phenolic extracts from Helicteres isora L. and Ceiba pentandra L. Journal of Food Science and Technology, 50(4), 687–695.
27. Shah, N. A., Khan, M. R., & Nigussie, D. (2017). Phytochemical investigation and nephroprotective potential of Sida cordata in rat. BMC Complementary and Alternative Medicine, 17(1), 388.
28. Haule, E. E., Moshi, M. J., Nondo, R. S. O., Mwangomo, D. T., & Mahunnah, R. L. A. (2012). A study of antimicrobial activity, acute toxicity and cytoprotective effect of a polyherbal extract in a rat ethanol-HCl gastric ulcer model. BMC Research Notes, 5, 546.
29. Wink, M. (2015). Modes of action of herbal medicines and plant secondary metabolites. Medicines, 2(3), 251–286.
30. Dinda, B., Das, N., Dinda, S., Dinda, M., & Silsarma, I. (2015). The genus Sida L.—A traditional medicine: Its ethnopharmacological, phytochemical and pharmacological data for commercial exploitation in herbal drugs industry. Journal of Ethnopharmacology, 176, 135–176.
31. Yahfoufi, N., Alsadi, N., Jambi, M., & Matar, C. (2018). The immunomodulatory and anti-inflammatory role of polyphenols. Nutrients, 10(11), 1618.
32. Číž, M., Dvořáková, A., Skočková, V., & Kubala, L. (2020). The role of dietary phenolic compounds in epigenetic modulation involved in inflammatory processes. Antioxidants, 9(7), 691.
33. Olas, B. (2020). Honey and its phenolic compounds as an effective natural medicine for cardiovascular diseases in humans. Nutrients, 12(2), 283.
34. Chisom, I. F., Okereke, C., & Okeke, C. (2014). Comparative phytochemical and proximate analyses on Ceiba pentandra (L.) and Bombax buonopozense (P.) Beauv. Journal of Pharmacognosy and Phytochemistry, 2(6), 162–167.
35. Denizot, F., & Lang, R. (1986). Rapid colorimetric assay for cell growth and survival: Modifications to the tetrazolium dye procedure giving improved sensitivity and reliability. Journal of Immunological Methods, 89(2), 271–277.
36. Kim, Y. S., Kim, E. K., Nawarathna, W. P. A. S., Dong, X., Shin, W. B., Park, J. S., Moon, S. H., Park, P. J. (2017). Immune-stimulatory effects of Althaea rosea flower extracts through the MAPK signaling pathway in RAW264.7 cells. Molecules, 22(4), 679.
37. Park, J. W., Kwon, O. K., Jang, H., Jeong, H., Oh, S. R., Lee, H. K., Han, S. B., & Ahn, K. S. (2012). A leaf methanolic extract of Wercklea insignis attenuates the lipopolysaccharide-induced inflammatory response by blocking the NF-κB signaling pathway in RAW 264.7 macrophages. Inflammation, 35(1), 321–331.
38. Lima, A. L. A., Alves, A. F., Xavier, A. L., Mozzini-Monteiro, T., Oliveira, T. R. R., Leite, F. C., et al. (2016). Anti-inflammatory activity and acute toxicity studies of hydroalcoholic extract of Herissantia tiubae. Revista Brasileira de Farmacognosia, 26(2), 225–232.
39. Lin, H. H., Huang, H. P., Huang, C. C., Chen, J. H., & Wang, C. J. (2005). Hibiscus polyphenol-rich extract induces apoptosis in human gastric carcinoma cells via p53 phosphorylation and p38 MAPK/FasL cascade pathway. Molecular Carcinogenesis, 43(2), 86–99.
40. Kumar, R., Kumar, N., Ramalingayya, G. V., Setty, M. M., & Pai, K. S. R. (2016). Evaluation of Ceiba pentandra (L.) Gaertner bark extracts for in vitro cytotoxicity on cancer cells and in vivo antitumor activity in solid and liquid tumor models. Cytotechnology, 68(6), 1909–1923.
41. Johnson, G. L., & Lapadat, R. (2002). Mitogen-activated protein kinase pathways mediated by ERK, JNK, and p38 protein kinases. Science, 298(5600), 1911–1912.
42. Paul, M. K., & Mukhopadhyay, A. K. (2012). Tyrosine kinase—Role and significance in cancer. International Journal of Medical Sciences, 1(2), 101–115.
43. He, L., Pei, H., Lan, T., Tang, M., Zhang, C., & Chen, L. (2017). Design and synthesis of a highly selective JAK3 inhibitor for the treatment of rheumatoid arthritis. Archiv der Pharmazie, 350(12), 1700194.
44. Roy, P. K., Rashid, F., Bragg, J., & Ibdah, J. A. (2008). Role of the JNK signal transduction pathway in inflammatory bowel disease. World Journal of Gastroenterology, 14(2), 200–202.
45. Mitsuyama, K., Suzuki, A., Tomiyasu, N., Tsuruta, O., Kitazaki, S., Takeda, T., & Satoh, Y. (2006). Pro-inflammatory signaling by Jun-N-terminal kinase in inflammatory bowel disease. International Journal of Molecular Medicine, 17(3), 449–455.
46. Chen, H. J., Lin, C. M., Lee, C. Y., Shih, N. C., Peng, S. F., Tsuzuki, M., et al. (2013). Kaempferol suppresses cell metastasis via inhibition of the ERK-p38-JNK and AP-1 signaling pathways in U-2 OS human osteosarcoma cells. Oncology Reports, 30(2), 925–932.
47. Yoon, H. Y., Lee, E. G., Lee, H., Cho, I. J., Choi, Y. J., Sung, M. S., et al. (2013). Kaempferol inhibits IL-1β-induced proliferation of rheumatoid arthritis synovial fibroblasts and the production of COX-2, PGE2 and MMPs. International Journal of Molecular Medicine, 32(5), 971–977.
48. Chen, X., Yang, X., Liu, T., Guan, M., Feng, X., Dong, W., et al. (2012). Kaempferol regulates MAPKs and NF-κB signaling pathways to attenuate LPS-induced acute lung injury in mice. International Immunopharmacology, 14(2), 209–216.
49. Yang, Y., Li, Y., Wang, K., Wang, Y., Yin, W., & Li, L. (2013). P38/NF-κB/Snail pathway is involved in caffeic acid-induced inhibition of cancer stem cells-like properties and migratory capacity in malignant human keratinocytes. PLOS ONE, 8(4), e58915.
50. Rivera, L., Morón, R., Sánchez, M., Zarzuelo, A., & Galisteo, M. (2008). Quercetin ameliorates metabolic syndrome and improves the inflammatory status in obese Zucker rats. Obesity, 16(9), 2081–2087.
51. Feghali, C. A., & Wright, T. M. (1997). Cytokines in acute and chronic inflammation. Frontiers in Bioscience, 2, d21–d26.
52. Brenner, D., Blaser, H., & Mak, T. W. (2015). Regulation of tumour necrosis factor signaling: Live or let die. Nature Reviews Immunology, 15(6), 362–374.
53. Fehr, S., Unger, A., Schaeffler, E., Herrmann, S., Laufer, S., Schwab, M., & Albrecht, W. (2015). Impact of p38 MAP kinase inhibitors on LPS-induced release of TNF-α in whole blood and primary cells from different species. Cellular Physiology and Biochemistry, 36(6), 2237–2249.
54. Bhattacharyya, S., Brown, D. E., Brewer, J. A., Vogt, S. K., & Muglia, L. J. (2007). Macrophage glucocorticoid receptors regulate Toll-like receptor 4-mediated inflammatory responses by selective inhibition of p38 MAP kinase. Blood, 109(10), 4313–4319.
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