Sains Malaysiana 38(5)(2009): 773–784

 

Chlorella vulgaris Menunjukkan Kesan Antioksidan dan Antitumor Terhadap Kanser Hepar dalam Kajian in vivo dan in vitro

(Chlorella vulgaris Exhibited Antioxidant and Antitumour Effects against Liver

Cancer in in vivo and in vitro Studies)

 

 

Nor Ashikeen Mukti, Suhaniza Sulaiman, Suhana Md Saad, Junaida @ Maimunah Hassan Basari, Mariati Abdul Rahman, Wan Zurinah Wan Ngah, Yasmin Anum Mohd Yusof*

Jabatan Biokimia Fakulti Perubatan

Pusat Perubatan Universiti Kebangsaan Malaysia

Jalan Raja Muda Abdul Aziz, 50300 Kuala Lumpur, Malaysia

 

 

Received: 7 October 2008 / Accepted: 22 April 2009

 

ABSTRAK

 

Chlorella vulgaris (ChV), sejenis alga hijau unisel telah dilaporkan mempunyai khasiat kesihatan pada penyakit tertentu termasuk kanser. Objektif utama kajian ialah untuk mengukur dan menilai kesan antioksidan dan antitumor ekstrak air panas ChV ke atas sel kanser hepar yang dijalankan secara in vivo dan in vitro. Asai DPPH yang dijalankan menunjukkan peratus pengautan ChV yang tinggi. Dalam kajian in vivo, tikus Wistar jantan (200-250 g) dibahagikan kepada lapan kumpulan: tikus kawalan (diet normal), tikus diaruh kanser hepar (diet kurang kolin + 0.1% etionin dalam air minuman) atau singkatannya CDE, tikus diberi rawatan ChV pada tiga dos berbeza (50, 150 dan 300 mg/kg berat badan) dan tikus CDE diberi rawatan ChV pada tiga dos berbeza. Sampel darah dan tisu diambil dari semua kumpulan tikus pada minggu 0, 4, 8 dan 12 untuk penentuan kadar proliferasi dan apoptosis sel untuk melihat kesan antitumor ChV. Peratus pembentukan nodul praneoplasia adalah tinggi pada tikus diaruh kanser hepar (CDE) tetapi ChV pada semua dos berjaya mengurangkannya. Pertambahan jumlah sel kanser semasa hepatokarsinogenesis ditunjukkan dengan peningkatan proliferasi hepatosit yang signifikan (p<0.05) pada tikus CDE berbanding kawalan tetapi ChV pada semua dos berjaya mengurangkan proliferasi secara signifikan (p<0.05). Peratus apoptosis sel didapati meningkat secara signifikan (p<0.05) pada tikus CDE, tetapi peningkatan yang lebih ketara berlaku pada tikus CDE diberi ChV (300 mg/kg berat badan). Dalam kajian in vitro pula, aktiviti antitumor ekstrak air panas ChV telah ditentukan dengan melihat perubahan dalam proliferasi dan apoptosis sel kanser hepar HepG2 yang dikultur di makmal. Ekstrak air panas ChV berjaya menurunkan kadar proliferasi sel HepG2 dengan signifikan secara berkadar terus dengan dos yang digunakan dengan nilai IC50 1.6 mg/ml. Hasil analisis TUNEL pula menunjukkan ekstrak air panas ChV berjaya mengaruh apoptosis dalam sel HepG2. Keputusan ini disokong oleh hasil pemblotan Western dengan peningkatan pengekspresan protein P53 dan protein proapoptosis BAX dan Kaspase-3. Daripada hasil-hasil kajian, dapatlah dicadangkan bahawa ChV berpotensi tinggi sebagai antioksidan serta berupaya memberi kesan antitumor kepada kanser hepar pada kajian in vivo dan in vitro.

 

Kata kunci: antioksidan; antitumor; apoptosis; Chlorella vulgaris; kanser hepar; proliferasi

 

ABSTRACT

 

The unicellular green microalgae Chlorella vulgaris (ChV) has been reported to have beneficial effects on various diseases including cancer. The main objectives of this study were to determine and evaluate the antioxidant and antitumour properties of ChV against liver cancer cells, both in vivo and in vitro. The antioxidant effect of hot water extract of ChV was demonstrated by DPPH assay which exhibited a high percentage of free radical scavenging activity. In in vivo studies, male Wistar rats (200-250 g) were divided into eight groups according to the diet given: control group (normal diet), liver cancer (choline deficient diet + 0.1% ethionine in drinking water to induce liver cancer), abbreviated as CDE group, ChV group with three different doses (50, 150 and 300 mg/kg body weight), and CDE group treated with three different doses of ChV. Rats were killed at 0, 4, 8 and 12 weeks of experiment and blood and tissue samples were taken from the rats in all groups for the determination of cellular proliferation and apoptosis. ChV at all doses reduced the percentage of liver tumour incidence (the preneoplastic nodules) in the CDE (liver cancer) rats when compared to the CDE rats alone. The percentage of hepatocyte proliferation was significantly higher (p<0.05) in CDE rats when compared to control which however was inhibited by ChV at all doses. Meanwhile, the percentage of apoptotic cells in the CDE rats increased significantly (p<0.05) compared to control which was further increased when treated with higher dosage of ChV (300 mg/kg body wt). The antitumour effects of hot water extract of ChV in in vitro studies were determined by observing the changes in the proliferation and apoptosis rate in liver cancer cell line, HepG2. ChV reduced (p<0.05) the proliferation rate of HepG2 cells in dose-dependent manner. The IC50 value was recorded at 1.6 mg/ml. Apoptosis was induced by ChV, as indicated by TUNEL analysis which was supported further by Western blot analysis indicating increased expression of P53 and pro-apoptotic proteins BAX, and Caspase-3. From these findings, it can be suggested that ChV has great potential as an antioxidant with the ability to exert antitumour effects against liver cancer.

 

Keywords: Antioxidant; antitumour; apoptosis; Chlorella vulgaris; liver cancer; proliferation

 

REFERENCES

 

Akhurst, B., Croager, E.J., Farley-Roche, C.A., Ong J.K., Dumble, M.L., Knight, B. & Yeoh, G.C. 2001. A modified choline-deficient, ethionine-supplemented diet protocol effectively induces oval cells in mouse liver. Hepatology 34: 519-522.

Bonham, M., Arnold, H., Montgomery, B. & Nelson, P.S. 2002. Molecular effects of the herbal compound PC-SPES: identification of activity pathways in prostate carcinoma. Cancer Research 62: 3920-24.

Bortner, C.D., Oldenburg, N.B.E. & Cidlowski, J.A. 1995. Trends in Cell Biology 5: 21-26

Cherng, J-Y. & Shih, M-F. 2005. Potential hypoglycemic effects of Chlorella in streptozotocin-induced diabetic mice. Life Sciences 77(9): 980-990.

Cherng, J-Y. & Shih, M-F. 2006. Improving glycogenesis in Streptozocin (STZ) diabetic mice after administration of green algae Chlorella. Life Sciences 78: 1181-1186.

Choo, T.C. & Choo, H.L. 2004. Chlorella Nature’s Miraculous Gift to Mankind. Selangor: Uniwellness Resources.

Chowdhury, I., Tharakan, B. & Bhat, G.K. 2008. Caspases - An update. Comparative Biochemistry and Physiology, Part B. 51: 10-27.

Cook, B.B., Lau, E.W. & Baily, B.M. 1963. The protein quality of waste-grown green algae. Quality of protein in mixtures of algae, nonfat powdered milk, and cereals. Journal of Nutrition 81: 23-29.  

De Flora, S. & Ferguson, L.R. 2005. Overview of mechanisms of cancer chemopreventive agents. Mutation Research 591: 8-15.

Fang, Y.Z, Yang, S. & Wu, G. 2002. Free Radicals, Antioxidant, and Nutrition. Nutrition 18: 872-879.

Goodsell, D.S. 2002. The molecular perspective: Bcl-2 and apoptosis. Stem Cells 20(4): 355–356.

Hasegawa, T., Kimura, Y., Hiromatsu, K., Kobayashi, N., Yamada, A., Makino, M., Okuda, M., Sano, T., Nomoto, K. & Yoshikai, Y. 1997. Effect of hot water extract of Chlorella vulgaris on cytokine expression patterns in mice with murine acquired immunodeficiency syndrome after infection with Listeria monocytogenes. Immunopharmacology 35: 273-282.

Hasegawa, T., Matsuguchi, T., Noda, K., Tanaka, K., Kumamoto, S., Shoyama, Y. & Yoshikai, Y. 2002. Toll – like receptor 2 is at least partly involved in the antitumor activity of glycoprotein from Chlorella vulgaris. International Immunopharmacology 2(4): 579-589.

Hasegawa, T., Noda, K., Kumamoto, S., Ando, Y., Yamada, A. & Yoshikai, Y. 2000. Chlorella vulgaris culture supernatant (CHVS) reduces phycological stress - induced apoptosis in thymocytes of mice. International Journal of Immunopharmacology 22: 877-885.

Hasegawa, T., Yoshikai, Y., Okuda, M. & Nomoto, K. 1990. Accelerated restoration of the leukocyte number and augmented resistance against Escherichia coli in cyclophosphamide-treated rats orally administered with a hot water extract of Chlorella vulgaris. International Journal of Immunopharmacology 12(8): 883-891.

Hocman G. 1989. Prevention of cancer: Vegetables and plants. Comparative Biochemistry and Physiology 93B(2): 201-212.

Holland, B.K. & Frei, P.W. 2000. Tumor Growth & Cell Proliferation In Vivo. (accessed online) http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=cmed.section. 175 (9 Mac 2006).

Hu, H., Ahn, N.S., Yang, X., Lee, Y.S. & Kang K.S. 2002. Ganoderma lucidum extract induces cell cycle arrest and apoptosis in MCF-7 human breast cancer cell. International Journal of Cancer 102: 250-253.

Huang, S.T., Yang, R.C., Yang, L.J., Lee, P.N. & Pang, J.H.S. 2003. Phylanthus urinaria triggers the apoptosis and Bcl-2 down-regulation in Lewis lung carcinoma cells. Life Sciences 72: 1705-1716.

Jia, G., Tohyama, C. & Sone, H. 2002. DNA damage triggers imbalance of proliferation and apoptosis during development of preneoplastic foci in the liver of Long-Evans Cinnamon rats. International Journal of Oncology 21: 755-761

Khan, N., Afaq, F., Mukhtar, H. 2007. Apoptosis by dietary factors: the suicide solution for delaying cancer growth. Carcinogenesis 28(2): 233-239.

Kim, E.J., Lee, Y.J., Shin, H.K. & Park, J.H.Y. 2005. Induction of apoptosis by the aqueous extract of Rubus coreanum in HT-29 human colon cancer cells. Nutrition 21: 1141-1148.

Klaunig, J.E. & Kamendulis, L.M. 1999. Mechanisms of Cancer Chemoprevention in Hepatic Carcinogenesis: Modulation of Focal Lesion Growth in Mice. Toxicological Sciences 52: 101-106

Kluck, R.M., Bossy-Wetzel, E., Green, D.R., Newmeyer, D.D. 1997. The release of cytochrome c from mitochondria: a primary site for Bcl-2 regulation of apoptosis. Science 275 (5303): 1132-1136.

Konishi, F., Tanaka, K., Himeno, K., Taniguchi, K. & Nomoto, K. 1985. Antitumor effect induced by a hot water extract of Chlorella vulgaris (CE): Resistance to Meth-A tumor growth mediated by CE-induced polymorphonuclear leukocytes. Cancer Immunology Immunotherapy 19: 73-78

Kralovec, J.A., Power, M.R., Liu, F., Maydanski, E., Ewart, H.S. Watson, L.V., Barrow, C.J. & Lin, T.J. 2005. An aqueous Chlorella extract inhibit IL-5 production by mast cells in vitro and reduces ovalbumin-induced eosinophil infiltration in the airway in mice in vivo. International Immunopharmacology 5: 689-698

Lai, L.S., Chou, S.T. & Chao, W.W. 2001. Studies on the antioxidative activities of hsian-tsao (Mesona procumbens) leaf gum. Journal of Agricultural and Food Chemistry 49(2): 963-968.

Lau, B.H.S., Lau, E.W. & Yamasaki, T. 1992. Edible plant extracts modulate macrophage activity and bacteria mutagenesis. International Clinical Nutrition Review 12(3): 147.

Ledda-Columbano, G. M. & Columbano, A. 1991. Apoptosis and Hepatocarcinogenesis. Apoptosis: The Molecular Basis of Cell Death. Itali: Cold Spring Harbor Laboratory Press.

Lee, S.M.Y., Li, M.L.Y., Tse, Y.C., Leung, S.C.L., Lee, M.M.S., Tsui, S.K.W., Fung, K.P., Lee, C.Y. & Waye, M.M.Y. 2002. Paeoniae Radix, a Chinese herbal extract, inhibit hepatoma cells growth by inducing apoptosis in a p53 independent pathway. Life Sciences 71: 2267-2277.

Li, R., Hehlmanb, R., Sachsc, R. & Duesberg, P. 2005. Chromosomal alterations cause the high rates and wide ranges of drug resistance in cancer cells. Cancer Genetics and Cytogenetics 163: 44-56.

Lim, G.C.C. & Halimah, Y. 2004. Second Report of National Cancer Registry. Cancer Incidence in Malaysia 2003. Kuala Lumpur: National Cancer Registry.

Liu, X., Zou, H., Slaughter, C. & Wang, X. 1997. DFF, a Heterodimeric Protein That Functions Downstream of Caspase-3 to Trigger DNA Fragmentation during Apoptosis. Cell 89: 175-184.

Llovet, J.M., Burroughs, A. & Bruix, J. 2003. Hepatocellular carcinoma. Lancet 362: 1907-1917.

Lu, Y. R. & Foo, L. Y. 2000. Antioxidant and radical scavenging activities of polyphenols from apple pomace. Food Chemistry 68: 81-85.

May, P. & May, E. 1999. Twenty years of p53 research: structural and functional aspects of the p53 protein. Oncogene 18(53): 7621-7636.

Mori, H., Sugie, S., Yoshimi, N., Hara, A. & Tanaka, T. 1999. Control of cell proliferation in cancer prevention. Mutation Research 428: 291-298.

Morimoto, T., Nagatsu, A., Murakami, N., Sakakibara, J., Tokuda, H., Nishino, H. & Iwashima A. 1995. Anti-Tumour-Promoting Glycerolglycolipids from the Green Alga, Chlorella vulgaris. Phytochemistry 40(5): 1433-1437

Noda, K., Ohno, N., Tanaka, K., Okuda, M., Yadomae, T., Nomoto, K. & Shoyama, Y.A. 1996. Water soluble antitumor glycoprotein from Chlorella vulgaris. Planta Medica 62: 423-426.

Park, J-Y., Cho, H-Y., Kim, J-K., Noh, K-H., Yang, J-R., Ahn, J-M., Lee, M-O. & Song,Y-S. 2005. Chlorella dichloromethane extract ameliorates NO production and iNOS expression through the down-regulation of NFκB activity mediated by suppressed oxidative stress in RAW 264-7 macrophage. Clinica Chimica Acta 351(1-2): 185-196.

Pitot, H.C., Hikita, H., Dragan, L., Sargent, L. & Haas, M. 2000. Review article: the stages of gastrointestinal carcinogenesis – application of rodent models to human disease. Alimentary Pharmacology & Therapeutics 14(1): 153-160.

Rodriguez-Garcia, I. & Guil-Guerrero, J.L.2008. Evaluation of the antioxidant activity of three alga species for use as dietary supplements and in the preservation of foods. Food Chemistry 108: 1023-1026.

Romeo, R. & Colombo, M. 2002. The natural history of hepatocellular carcinoma. Toxicology 182: 39-42.

Schafer, D.F & Sorrell, M.F. 1999. Hepatocellular carcinoma. Lancet 353: 1253-1257.

Schulte-Hermann, R., Bursch, W. & Grasl-Kraupp, B. 1995. Active Cell Death (Apoptosis) in Liver Biology and Disease. Progress in Liver Diseases XIII: 1-35.

Shahidi, F. 1997. Natural Antioxidants: An Overview. Dlm: Shahidi, F. Natural Antioxidants: Chemistry, Health Effects and Applications, hlm. 1-11. Champaign Illinois: AOCS Press.

Surh, Y-J. 1999. Molecular mechanisms of chemopreventive effects of selected dietary and medicinal phenolic substances. Mutation Research 428: 305-327.

Surh, Y-J. 2002. Anti-tumor promoting potential of selected spice ingredients with antioxidative and anti-inflamatory activities: A short review. Food and Chemical Toxicology 40: 1091-1097.

Tanaka, K., Tomita, Y., Tsuruta, M., Konishi, F., Okuda, M., Himeno, K. & Nomoto, K. 1990. Oral administration of Chlorella vulgaris augments concomitant antitumor immunity. Immunopharmacology Immunotoxicology 12 (2): 277-291.

Tanaka, K., Yamada, A., Noda, K., Hasegawa, T., Okuda, M. & Shoyama, Y. 1998. A novel glycoprotein obtained from Chlorella vulgaris strain CK22 shows antimetastatic immunopotentiation. Cancer Immunology Immunotherapy 45: 313-320.

Tessitore, L. 2000. Apoptosis and cell proliferation are involved in the initiation of liver carcinogenesis by a subnecrogenic dose of diethylnitrosamine in refed rats. Journal of Nutrition 130: 104-110.

Winter, J.D. 1986. The nature of cancer. Dlm. The truth about cancer: A personal guide to causes and treatment. Blandford Press. Sidney: Bliddles Ltd, Guildford. 15-20.

Yamagishi, S., Nakamura, K. & Inoue, H. 2005. Therapeutic potentials of unicellular green alga Chlorella in advanced glycation end product (AGE)-related disorders. Medical Hypotheses 65: 953-955.

Zakeri, Z. & Lockshin, R.A. 2002. Cell death during development. Journal of Immunological Methods 265: 3-20.

Zhivotovsky, B., Orrenius, S., Brustugun, O.T. & Doskeland, S.O. 1998. Injected cytochrome induces apoptosis. Nature 391: 449-450.

 

 

*Corresponding author; email: anum@medic.ukm.my

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