Abstract
Ulva fasciataDelile, a marine macroalga is abundantly available on the intertidal rocky surface of Visakhapatnam coasts, India, during summer. The algae belong to family Ulvaceae and division Chlorophyta is glossy green in color. Being a prolific source of bioactive compounds, this thallus allured an unprecedented concern of the author to study its anatomy, histo-chemistry and in-vivo anticancer property. Primarily, the morpho-anatomy and histo-chemistry of the thallus were studied to identify correct species and locate the active phytoconstituents in the cell saps. Besides, the in-vivo anticancer activity of the methanolic algal extract (MAE) was studied on Ehrlich’s ascites carcinoma (EAC) xenografted mice. The light microscopy of the thallus divulged very thick cuticularized layers in the sectional view. A fat middle lamella was observed in between two layers of vertically oblong palisade cells. The histo-chemistry revealed the presence of starch grains, calcium oxalate crystals, tannin, protein,and lipids as major cell inclusions. The extract exhibited a profound inhibitory activity on EAC xenografted mice (p˂0.001). Increase in mean survival time (p˂0.001) and restoration of the hematological parameter in drug-treated rodents were clear indicators of anticancer potential of the MAE. It was espoused by the results garnered from various parameters like reduced ascites tumor volume, declined peritoneal cavity size, the percentage increase in life span (%ILS), declined cell viability andperitoneal angiogenesis, and the improved result obtained from histopathology of vital organs.
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References
Agrawal SS, Saraswati S, Mathur R, Pandey M (2011) Antitumor properties of Boswellic acid against Ehrlich ascites cells bearing mouse. Food Chem Toxicol 49(9):1924–1934. https://doi.org/10.1016/j.fct.2011.04.007
Ahmed OM, Ahmed RR (2014) Anti-proliferative and apoptotic efficacies of ulvan polysaccharides against different types of carcinoma cells In Vitro and In Vivo. J Cancer Sci Ther 6:202–208. https://doi.org/10.4172/1948-5956.1000272
Akbari V, Zafari S, Yegdaneh A (2018) Anti-tuberculosis and cytotoxic evaluation of the seaweed Sargassum boveanum. Res Pharm Sci 13(1):30–37. https://doi.org/10.4103/1735-5362.220965
Alves C, Pinteus S, Rodrigues A, Horta A, Pedrosa R (2018) Algae from portuguese coast presented high cytotoxicity and antiproliferative effects on an in vitro model of human colorectal cancer. Pharmacognosy Res 10(1):24–30. https://doi.org/10.4103/pr.pr_151_16
Anand K, Sarkar A, Kumar A, Ambasta RK, Kumar P (2012) Combinatorial antitumor effect of naringenin and curcumin elicit angioinhibitory activities in vivo. Nutr Cancer 64(5):714–724. https://doi.org/10.1080/01635581.2012.686648
Bala A, Kar B, Haldar PK, Mazumder UK, Bera S (2010) Evaluation of anticancer activity of cleome gynandra on ehrlich’s ascites carcinoma treated mice. J Ethnopharmacol 129:131–134. https://doi.org/10.1016/j.jep.2010.03.010
Balasubashini MS, Karthigayan S, Somasundaram ST, Balasubramanian T, Viswanathan V, Raveendrand P et al (2006) Fish venom (Pterios volitans) peptide reduces tumor burden and ameliorates oxidative stress in Ehrlich’s ascites carcinoma xenografted mice. Bioorg Med Chem Lett 16:6219–6225. https://doi.org/10.1016/j.bmcl.2006.09.025
Barahona T, Chandía NP, Encinas MV, Matsuhiro B, Zúñiga EA (2011) Antioxidant capacity of sulfated polysaccharides from seaweeds. A kinetic approach. Food Hydrocolloids 25:529–535. https://doi.org/10.1016/j.foodhyd.2010.08.004
Bhattacharjee A, Basu A, Biswas J, Sen T, Bhattacharya S (2017) Chemoprotective and chemosensitizing properties of selenium nanoparticle (Nano-Se) during adjuvant therapy with cyclophosphamide in tumor-bearing mice. Mol Cell Biochem 424(1–2):13–33. https://doi.org/10.1007/s11010-016-2839-2
Brain KR, Turner TD (1975) The practical evaluation of phytopharmaceuticals. Wright-Scientechnica, Bristol
Chakkere Shivamadhu M, Srinivas BK, Jayarama S, Angatahalli Chandrashekaraiah S (2017) Anti-cancer and anti-angiogenic effects of partially purified lectin from Praecitrullus fistulosus fruit on in vitro and in vivo model. Biomed Pharmaco Ther 96:1299–1309. https://doi.org/10.1016/j.biopha.2017.11.082
Chakraborty K, Paul raj R (2010) Sesquiterpenoids with free-radical-scavenging properties from marine macroalga Ulva fasciata Delile. Food Chem 122:31–41. https://doi.org/10.1016/j.foodchem.2010.02.012
Chakraborty K, Lipton AP, Paul Raj R, Vijayan KK (2010a) Antibacterial labdane diterpenoids of Ulva fasciata Delile from southwestern coast of the Indian Peninsula. Food Chem 119:1399–1408. https://doi.org/10.1016/j.foodchem.2009.09.019
Chakraborty K, Lipton AP, Paulraj R, Chakraborty RD (2010b) Guaiane sesquiterpenes from seaweed Ulva fasciata Delile and their antibacterial properties. Eur J Med Chem 45:2237–2244. https://doi.org/10.1016/j.ejmech.2010.01.065
Dashek WV (2000) Methods in plant electron microscopy and cytochemistry. Humana Press. https://doi.org/10.1007/978-1-59259-232-6
Das MK, Sahu PK, Rao GS, Mukkanti K, Silpavathi L (2014) Application of response surface method to evaluate the cytotoxic potency of Ulva fasciataDelile, a marine macro alga. Saudi J Biol Sci 21(6):539–546. https://doi.org/10.1016/j.sjbs.2014.02.003
Fahn A (1982) Plant anatomy. Pergamon Press, Oxford
Folkman J (2002) Role of angiogenesis in tumor growth and metastasis. Semin Oncol 29(6 Suppl 16):15–18. https://doi.org/10.1053/sonc.2002.37263
Garg HS, Sharma M, Dewan SB, Pramanik BN, Bose AK (1992) An antiviral sphingosine derivative from the green alga Ulva Fasciata. Tetrahedron Lett 33:1641–1644. https://doi.org/10.1016/S0040-4039(00)91695-2
Gerwick WH, Moore BS (2012) Lessons from the past and charting the future of marine natural products drug discovery and chemical biology. Chem Biol 19:85–98. https://doi.org/10.1016/j.chembiol.2011.12.014
Ghannadi A, Shabani L, Yegdaneh A (2016) Cytotoxic, antioxidant and phytochemical analysis of Gracilaria species from Persian Gulf. Adv Biomed Res 5:139. https://doi.org/10.4103/2277-9175.187373
Ghosh M, Talukdar D, Ghosh S, Bhattacharyya N, Ray M, Ray S (2006) In vivo assessment of toxicity and pharmacokinetics of methylglyoxal, Augmentation of the curative effect of methylglyoxal on cancer-bearing mice by ascorbic acid and creatine. Toxicol Appl Pharmacol 212(1):45–58. https://doi.org/10.1016/j.taap.2005.07.003
Gupta M, Mazumder UK, Sambath Kumar R, Siva Kumar T, Vamsi MLM (2004) Antitumor activity and antioxidant status of Caesalpinia bonducella against Ehrlich ascites carcinoma in Swiss albino mice. J Pharmacol Sci 94:77–184. https://doi.org/10.1254/jphs.94.177
Haefner B (2003) Drugs from the deep: marine natural products as drug candidates. DDT 8:536–544. https://doi.org/10.1016/S1359-6446(03)02713-2
Johansen DA (1940) Plant micro techniques. Mc Grew Hill Book co. New York, USA
Kviecinski MR, Felipe KB, Schoenfelder T, de Lemos Wiese LP, Rossi MH, Gonçalez E, FelicioJD FDW, Pedrosa RC (2008) Study of the antitumor potential of Bidenspilosa (Asteraceae) used in Brazilian folk medicine. J Ethnopharmacol 117(1):69–75. https://doi.org/10.1016/j.jep.2008.01.017
Liu M, Hansen PE, Lin X (2011) Bromophenols in marine algae and their bioactivities. Marine Drugs 9:1273–1292. https://doi.org/10.3390/md9071273
O’Brien TP, Feder N, McCully ME (1964) Polychromatic staining of plant cell walls by toluidine blue O. Protoplasma 59:368–373. https://doi.org/10.1007/BF01248568
Palanisamy SK, Arumugam V, Rajendran S, Ramadoss A, Nachimuthu S, Peter DM, Sundaresan U (2018) Chemical diversity and anti-proliferative activity of marine algae. Nat Prod Res 25:1–5. https://doi.org/10.1080/14786419.2018.1488701
Patra S, Muthuraman MS, Prabhu AR, Priyadharshini RR, Parthiban S (2015) Evaluation of antitumor and antioxidant activity of Sargassum tenerrimum against Ehrlichascites carcinoma in mice. Asian Pac J Cancer Prev 16(3):915–921
Qureshi S, Al-Harbi MM, Ahmed MM, Raza M, Giangreco AB, Shah AH (1993) Evaluation of the genotoxic, cytotoxic and antitumor properties of Commiphoramolmol using normal and Ehrlich ascites carcinoma cell bearing Swiss albino mice. Cancer Chemother. Pharmacol 33:130–138. https://doi.org/10.1007/bf00685330
Rajeshkumar NV, Joy KL, Kuttan G, Ramsewak RS, Nair MG, Kuttan R (2002) Antitumour and anticarcinogenic activity of Phyllanthus amarus Extract. J Ethnopharmacol 81:17–22. https://doi.org/10.1016/S0378-8741(01)00419-6
Selvin J, Huxley AJ, Lipton AP (2004) Immunomodulatory potential of marine secondary metabolites against bacterial diseases of shrimp. Aquaculture 230:241–248. https://doi.org/10.1016/S0044-8486(03)00427-7
Sharma PR, Mondhe DM, Muthiah S, Pal HC, Shahi AK, Saxena AK et al (2009) Anticancer activity of an essential oil from Cymbopogon flexuosus. Chemico-Biol Interact 179:160–168. https://doi.org/10.1016/j.cbi.2008.12.004
Shylesh BS, Padikkala J (2000) In-vitro cytotoxic and antitumor property of Emilia sonchifolia(L.) DC in mice. J Ethnopharmacol 73:495–500. https://doi.org/10.1016/S0378-8741(00)00317-2
Sreelatha S, Padma PR, Umasankari E (2011) Evaluation of anti-cancer activity of ethanol extract of Sesbania grandiflora (Agati Sesban) against Ehrlich ascites carcinoma in swiss albino mice. J Ethnopharmacol 134:984–987. https://doi.org/10.1016/j.jep.2011.01.012
Thomas TJ, Panikkar B, Subramoniam A, Nair MK, Panikkar KR (2002) Antitumour property and toxicity of BarringtoniaracemosaRoxb seed extract in mice. J Ethnopharmacol 82:223–227. https://doi.org/10.1016/S0378-8741(02)00074-0
Yuan YV, Walsh NA (2006) Antioxidant and antiproliferative activities of extracts from a variety of edible sea weeds. Food Chem Toxicol 44:1144–1150. https://doi.org/10.1016/j.fct.2006.02.002
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The animals were handled and cared as per the guidelines of the committee for control and supervision of experiments on animals (CPCSEA, New Delhi, India). Institutional Animal Ethical Committee approved all the experimental procedures on animals. The reference number is IAEC No- 1549/Po/a/11/CPCSEA/IAEC/0003.
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Mukesh Kumar Das has no conflict of interest. Lingarkar Silpavathi has no conflict of interest. Debajyoti Das has no conflict of interest.
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Das, M.K., Silpavathi, L. & Das, D. Pharmacognosy and In-vivo anticancer potential of an indigenous marine macroalga, Ulvafasciata Delile from Visakhapatnam coast, India. ADV TRADIT MED (ADTM) 21, 433–442 (2021). https://doi.org/10.1007/s13596-021-00594-3
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DOI: https://doi.org/10.1007/s13596-021-00594-3