SCREENING OF ANTI-COLON CANCER ACTIVITY BY USING HYDROALCOHOLIC EXTRACT OF BORASSUS FABILIFERS HOOT ON SWISS ALBINO MICE
DOI:
https://doi.org/10.22159/ajpcr.2025v18i7.54432Keywords:
Colorectal cancer, Borassus fabillifer, Hydro-alcoholic extract, Cancer therapiesAbstract
Objectives: This study addresses the escalating global incidence of colon cancer, recognized as the most prevalent cancer type. With approximately 4.6% of men and 4.2% of women diagnosed during their lifetime, the urgency to explore effective treatments becomes paramount, given the annual occurrence of 1.23 million new cases worldwide. The primary objective is to investigate the impact of the hydroalcoholic extract of Borassus flabellifer on altered hematological and biochemical parameters induced by azoxymethane (AOM)/dextran sulfate sodium (DSS), identifying potential hepatoprotective effects.
Methods: This research utilized 30 mice, with 24 receiving AOM injections and 6 serving as untreated healthy controls. The AOM-injected mice were further subdivided into groups, and treatment with B. flabellifer extract commenced on the 3rd day and spanned 70 days. DSS cycles were administered, and hematological and biochemical parameters were assessed. At the end of the experiment, mice were sacrificed, and the colorectal region was preserved for analysis.
Results: Results elucidate the AOM/DSS-induced alterations, including increased serum levels of alanine transaminase, aspartate transaminase, alkaline phosphatase, white blood cell, platelet count, and total protein, indicative of hepatic damage. Conversely, the hydroalcoholic extract significantly reduced these parameters, aligning with previous studies showcasing the plant’s anti-cancer activity. These findings highlight the pharmacological potential of *B. flabellifer* in mitigating colon cancer symptoms.
Conclusion: This research underscores the significance of B. flabellifer in countering the rise of colon cancer. The hydroalcoholic extract exhibits promising results in ameliorating AOM/DSS-induced alterations, providing a foundation for further exploration of its therapeutic potential. The study contributes valuable insights into the pharmacological properties of *B. flabellifer* and sets the stage for potential applications in cancer treatment.
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References
Alam MN, Bristi NJ, Rafiquzzaman M. Review on in vivo and in vitro methods evaluation of antioxidant activity. Saudi Pharm J. 2013;21(2):143-52. doi: 10.1016/j.jsps.2012.05.002, PMID 24936134
Al-Said MS, Mothana RA, Al-Yahya MM, Rafatullah S, Al-Sohaibani MO, Khaled JM, et al. GC-MS analysis: In vivo hepatoprotective and antioxidant activities of the essential oil of Achillea biebersteinii Afan. Growing in Saudi Arabia. Evid Based Complement Alternat Med. 2016;2016:1867048. doi: 10.1155/2016/1867048, PMID 27293452
Andersen PH, Poulsen E. Mutagenicity of flour from the palmyrah palm (Borassus flabellifer) in Salmonella Typhimurium and Escherichia coli. Cancer Lett. 1985;26(1):113-9. doi: 10.1016/0304-3835(85)90179-x, PMID 3882222
Brahman M. Indigenous medicinal plants for modern drug development programme: Revitalization of native health tradition. Adv Plant Sci. 2000;1391:1-10.
American Cancer Society. Colorectal Cancer Facts and Figures. Available from: https://www.cancer.org/research/cancer-facts-statistics/ colorectal-cancer-facts-figures.html [Last accessed on 2022 Mar 05].
Chu C, Xia L, Bal LP, Li P, Chen HB, Zhao ZZ. Authentication of the 31 species of toxic and potent Chinese Materia Medica by light microscopy, Part 3: Two species of T/PCMM from flowers and their common adulterants. Microsc Res Tech. 2009;72:454-63.
Devi S, Arseculeratne SN, Pathmanathan R, McKenzie IF, Pang TM. Suppression of cell-mediated immunity following oral feeding of mice with palmyrah (Borassus flabellifer L) flour. Aust J Exp Biol Med Sci. 1985;63(4):371-9. doi: 10.1038/icb.1985.43, PMID 2935135
Ellman GL, Courtney KD, Andres V Jr., Feather-Stone RM. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem Pharmacol. 1961;7(2):88-95. doi: 10.1016/0006- 2952(61)90145-9, PMID 13726518
Jerry A. A comprehensive review on the medicinal properties of Borassus flabellifer. J Acad Ind Res. 2018;7(7):93-7.
Kangwanpong D, Arseculeratne SN, Sirisinha S. Clastogenic effect of aqueous extracts of palmyrah (Borassus flabellifer) flour on human blood lymphocytes. Mutat Res. 1981;89(1):63-8. doi: 10.1016/0165- 1218(81)90131-2, PMID 7242546
Komala M, Ravishankar C, Jayaram A. Alleviative effect of herbal extract containing phytoconstituents of Bambusa vulgaris and Opuntia ficus-indica against AOM/DSS-induced colorectal carcinoma-bearing mice. Asian J Oncol. 2022;10. doi: 10.1055/s-0042-174572912. Manimekalai P, Kaveena R, Naveena S, Nivetha S, Nivetha N. A review on pharmacognostical and phytochemical study of (Digera muricata L). J Med Plants Stud. 2020;8(5):52-6. doi: 10.22271/plants.2020. v8.i5a.1196
Yoshikawa M, Xu F, Morikawa T, Pongpiriyadacha Y, Nakamura S, Asao Y, et al. Medicinal flowers. XII.1) new spirostane-type steroid saponins with antidiabetogenic activity from Borassus flabellifer. Chem Pharm Bull (Tokyo). 2007;55(2):308-16. doi: 10.1248/cpb.55.308
Misra HP, Fridovich I. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem. 1972;247(10):3170-5. doi: 10.1016/S0021-9258(19)45228-9, PMID 4623845
Morton JF. Notes on distribution, propagation and products of Borassus palms (Arecaceae). Econ Bot. 1988;42(3):420-41. doi: 10.1007/ BF02860166
Nadkarni KM. Indian Materia Medica. Vol. 1. Bombay: Popular Press Prakashan; 2002. p. 209-10.
Niedzwiecki A, Roomi MW, Kalinovsky T, Rath M. Anticancer efficacy of polyphenols and their combinations. Nutrients. 2016;8(9):552. doi: 10.3390/nu8090552, PMID 27618095
Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95(2):351-8. doi: 10.1016/0003-2697(79)90738-3, PMID 36810
Paschapur MS, Patil MB, Kumar R, Patil SR. Influence of ethanolic extract of Borassus flabellifer L. male flowers (inflorescences) on chemically induced acute inflammation and polyarthritis in rats. Int J PharmTech Res. 2000;1:551.
Paschapur MS, Patil S, Patil SR, Kumar R, Patil MB. Evaluation of the analgesic and antipyretic activities of ethanolic extract of male flower (inflorescences) of Borassus flabellifer L. (Arecaceae). Int J Pharm Pharm Sci. 2009;1:98-106.
Pattanaik C, Reddy CS, Dhal NK. Phytomedicinal study of coastal sand dune species of Orissa. Indian J Tradit Knowl. 2008;7:263-8.
Pushpangadan P, Iyengar PK, Damodaran VK. Role of Traditional Medicine in Primary Health Care. Science for Health. Kerala: State Committee on Science, Technology and Environment, Government of Kerala; 1995.
Révész L, Hiestand P, La Vecchia L, Naef R, Naegeli HU, Oberer L, et al. Isolation and synthesis of a novel immunosuppressive 17alpha-substituted dammarane from the flour of the palmyrah palm (Borassus flabellifer). Bioorg Med Chem Lett. 1999;9(11):1521-6. doi: 10.1016/ s0960-894x(99)00220-6, PMID 10386928
Sivaraj R, Balakrishnan A, Thenmozhi M, Venkatesh R. Preliminary phytochemical screening of Aegle marmelos, Ruta graveolens, Opuntia dellini, Euphorbia royleana and Euphorbia antiquorum. Int J Pharm Sci Res. 2011;2:146-50.
Sahni C, Shakil NA, Jha V, Gupta RK. Screening of nutritional, phytochemical, antioxidant and antibacterial activity of the roots of Borassus flabellifer (Asian Palmyra Palm). J Pharmacogn Phytochem. 2014;3:58-68.
Siegel R, Ma J, Zou Z, Jemal A. Cancer statistics, 2014. CA Cancer J Clin. 2014;64(1):9-29. doi: 10.3322/caac.21208, PMID 24399786
Siegel RL, Miller KD, Wagle NS, Jemal A. Cancer statistics, 2023. CA Cancer J Clin. 2023;73(1):17-48. doi: 10.3322/caac.21763, PMID 36633525
Sudhakara P, Kannan P, Obireddy K, Rajulu V. Organophosphorus and DGEBA resins containing clay nanocomposites: Flame retardant, thermal, and mechanical properties. J Mater Sci. 2011;46:5176-83.
Takahashi M, Mutoh M, Kawamori T, Sugimura T, Wakabayashi K. Altered expression of beta-catenin, inducible nitric oxide synthase and cyclooxygenase-2 in azoxymethane-induced rat colon carcinogenesis. Carcinogenesis. 2000;21(7):1319-27. doi: 10.1093/carcin/21.7.1319, PMID 10874009
Thaker AI, Shaker A, Rao MS, Ciorba MA. Modeling colitis-associated cancer with azoxymethane (AOM) and dextran sulfate sodium (DSS). J Vis Exp. 2012;(67):4100. doi: 10.3791/4100, PMID 22990604
Van Rheedes H. Hortus Malabaricus. Kerala: University of Kerala; 2013. p. 123-4.
Kapoor LD. Hand Book of Ayurvedic Medicinal Plants. New York: CRC Press; 2005. p. 82.
Vengaiah PC, Ravindrababu D, Murthy GN, Prasad KR. Jaggery from Palmyrah palm (Borassus flabellifer L.) - present status and scope. Indian J Tradit Knowl. 2013;12:714-7.
Zou DM, Brewer M, Garcia F, Feugang JM, Wang J, Zang R, et al. Cactus pear: A natural product in cancer chemoprevention. Nutr J. 2005;4:25. doi: 10.1186/1475-2891-4-25, PMID 16150152
Kumar AB, Kumar Gautam G, Salman BS. Development, optimization and evaluation of pulsatile drug delivery capsules loaded with carvedilol by applying quality by design. Int J Appl Pharm. 2022;14(1):213-20. doi: 10.22159/ijap.2022v14i1.43146
Mutiah R, Sukardiman MA, Milliana A, Rahmawati E, Fitrianingsih AA, Yueniwati Y. Network pharmacology, apoptosis, and cell cycle inhibition of sesquiterpene compounds from Qusthul Hindi root extract (Saussurea lappa) in breast cancer: An in silico and in vitro approach. Int J Appl Pharm. 2023;15(6):132-41. doi: 10.22159/ ijap.2023v15i6.48798
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