Anticancer Potential Of Dillenia Bracteata: Evaluation Of Methanol Extract And Its Isolated Compound In Ehrlich Ascites Carcinoma-Induced Swiss Albino Mice
Keywords:
Dillenia, EAC induced carcinoma, 5-FU, antioxidantAbstract
Background: Cancer poses a significant health issue worldwide even though chemotherapy treatment creates major side effects in patients. Scientists find interest in the cancer prevention value of Dillenia bracteata Wight through herbal medicine research. This research analyzes the antitumor effects of Dillenia bracteata when given to Swiss albino mice with Ehrlich Ascites Carcinoma.
Objective: This research studied how MEDB and IF-D affect tumor growth in mice with EAC carcinoma and their effects on blood health and cell life along with liver function and inflammation markers.
Methods: Methanol extract was prepared from the dried leaves of Dillenia bracteata (MEDB) and active principle compound (IF-D) were isolated through column chromatography. Our research investigated MEDB and IF-D doses that were safe in the mice and then grouped them for investigation of invivo activity in EAC induced carcinoma. Researchers evaluated tumor size, weight, survival length, cell viability and essential blood chemistry results for all mice included in the study. Our research examined inflammatory markers like IL-6 and TNF along with hepatic condition tests and antioxidants SOD, GSH, CAT, MDA, plus total protein and enzyme measurements.
Results: Both MEDB and IF-D treatment brought about significant tumor size reduction and weight loss while making EAC-induced mice live longer. The isolated compound IF-D treated cancer cells better than MEDB and standard drug 5-fluorouracil (5-FU) activity. The treatment with IF-D therapy reduced tumor living cells while improving blood parameters and PCV. IF-D demonstrated great anti-inflammatory properties when it lowered IL-6 and TNF-α activity and strengthened natural defenses against oxidative damage. Hepatic parameters recovered completely because IF-D restored regular SGPT SGOT and ALP test results.
Conclusion: Results showed that the compound IF-D from Dillenia bracteata reduced cancer cells effectively while maintaining safe properties to study further its use in treating cancer patients. Research studies should test the plant extract IF-D because it shows great promise to control cancer development and protect liver health
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S. Tagne, B. P. Telefo, J. N. Nyemb et al., “Anticancer and antioxidant activities of methanol extracts and fractions of some Cameroonian medicinal plants,” Asian Pacific Journal of Tropical Medicine, vol. 7, no. 1, pp. S442–S447, 2014.
Sumitra and K. Nagani, “In vitro and in vivo methods for anticancer activity evaluation and some Indian medicinal plants possessing anticancer properties: an overview,” Journal of Pharmacognosy and Phytochemistry, vol. 2, no. 2, pp. 140–152, 2013.
P. K. Mukherjee, V. Kumar, and P. J. Houghton, “Screening of Indian medicinal plants for acetylcholinesterase inhibitory activity,” Phytotherapy Research, vol. 21, no. 12, pp. 1142–1145, 2007.
R. Ganapathy, S. Sundara, S. Mohan, Kameshwaran. S., and C. Dhanapal, “In-vitro anti cancer and in-vitro antioxidant potency of roots of hydro alcoholic extract of Plectranthus vettiveroides,” International Journal of Phytopharmacology, vol. 6, no. 4, pp. 246–254, 2015.
Krishnamoorthy and P. Ashwini, “Anticancer activity of Cynodon dactylon L. extract on Ehrlich ascites carcinoma,” Journal of Environmental Research And Development, vol. 5, no. 3, pp. 551–557, 2011.
R. Haghighi, M. H. Asadi, H. Akrami, and A. Baghizadeh, “Anti-carcinogenic and anti-angiogenic properties of the extracts of Acorus calamus on gastric cancer cells,” Avicenna Journal of Phytomedicine, vol. 7, no. 2, pp. 145–156, 2017.
Chopra RN, Nayar SL, Chopra IC. Glossary of Indian Medicinal Plants. 2nd ed. Delhi, India: Council of Scientific & Industrial Research; 1956. p. 173.
Shama, S.N., 2019. Phytochemical screening and antioxidant activity of Dillenia bracteata. International Journal of Green Pharmacy (IJGP), 13(2), 12
Avinash Kumar Reddy, G., TrilokMitra, M., Shilpa, T., Shabnam, S., SatishBabu, K., Jyothi M Joy. 2012. Variation of Phenols, Flavonoids and Antioxidant Potential in Various Parts of Foeniculumvulgare on Drying. International Journal of Chemical and Pharmaceutical Sciences. 3(1):74-79.
Schlede, E., 2002. Oral acute toxic class method: OECD Test Guideline 423. Rapporti istisan, 41, pp.32-36.
A.H. M. K. Alam, A. S. M. S. Hossain, M. A. Khan et al., “The antioxidative fraction of white mulberry induces apoptosis through regulation of p53 and NFκB in EAC cells,” PLoS ONE, vol. 11, no. 12, 2016.
Parasuraman S, Raveendran R, Kesavan R. Blood sample collection in small laboratory animals. JPharmacol Pharmacother 2011;2:74-9.
Dolai N, Karmakar I, Suresh Kumar RB, Kar B, BalaA, Haldar PK. Evaluation of antitumor activity and in vivo antioxidant status of Anthocephalus cadamba on Ehrlich ascites carcinoma treated mice. J Ethnopharmacol 2012;142:865-70
Mukherjee KL. Medical laboratory technology. New Delhi: Tata McGraw Hill Publication; 1990. p. 224-32
Mourtzikou, A., Alepaki, M., Stamouli, M., Pouliakis, A., Skliris, A. and Karakitsos, P., 2014. Evaluation of serum levels of IL-6, TNF-α, IL-10, IL-2 and IL-4 in patients with chronic hepatitis. Inmunología, 33(2), pp.41-50.
Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys 1959;82:70-7.
Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the folin phenol reagent. J Biol Chem 1951;193:265-75.
M. A. Al-Mamun, J. Husna, M. Khatun et al., “Assessment of antioxidant, anticancer and antimicrobial activity of two vegetable species of Amaranthus in Bangladesh,” BMC Complementary and Alternative Medicine, vol. 16, no. 1, article no. 157, 2016.
Shama, S.N., 2019. Phytochemical screening and antioxidant activity of Dillenia bracteata. International Journal of Green Pharmacy (IJGP), 13(2), 12
Gao, Y., Yin, J., Rankin, G.O. and Chen, Y.C., 2018. Kaempferol induces G2/M cell cycle arrest via checkpoint kinase 2 and promotes apoptosis via death receptors in human ovarian carcinoma A2780/CP70 cells. Molecules, 23(5), p.1095.
Choi, J.B., Kim, J.H., Lee, H., Pak, J.N., Shim, B.S. and Kim, S.H., 2018. Reactive oxygen species and p53 mediated activation of p38 and caspases is critically involved in kaempferol induced apoptosis in colorectal cancer cells. Journal of agricultural and food chemistry, 66(38), pp.9960-9967.
Chen, J., Zhong, K., Qin, S., Jing, Y., Liu, S., Li, D. and Peng, C., 2023. Astragalin: A food-origin flavonoid with therapeutic effect for multiple diseases. Frontiers in Pharmacology, 14, p.1265960.
Saleh, N., Allam, T., Korany, R.M., Abdelfattah, A.M., Omran, A.M., Abd Eldaim, M.A., Hassan, A.M. and El-Borai, N.B., 2022. Protective and therapeutic efficacy of hesperidin versus cisplatin against ehrlich ascites carcinoma-induced renal damage in mice. Pharmaceuticals, 15(3), p.294.
Dang, Q., Song, W., Xu, D., Ma, Y., Li, F., Zeng, J., Zhu, G., Wang, X., Chang, L.S., He, D. and Li, L., 2015. Kaempferol suppresses bladder cancer tumor growth by inhibiting cell proliferation and inducing apoptosis. Molecular Carcinogenesis, 54(9), pp.831-840.
Kaur, S., Mendonca, P. and Soliman, K.F., 2024. The Anticancer Effects and Therapeutic Potential of Kaempferol in Triple-Negative Breast Cancer. Nutrients, 16(15), p.2392.
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