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dc.contributor.authorEkowati, Heny
dc.contributor.authorPrasasti, Eka
dc.contributor.authorWasito, Hendri
dc.date.accessioned2012-12-14T07:21:53Z
dc.date.available2012-12-14T07:21:53Z
dc.date.issued2012
dc.identifier.citationAggarwal, B.B., Kunnumakkara, A.B., Harikumar, K.B., Tharakan, S.T., Sung, B., dan Anand, P., 2008, Potential of Spice-Derived Phytochemicals for Cancer Prevention, Planta Med, 74,1560–1569. Anonim, 2007, Indonesia Health Profile 2005, 70, Departemen Kesehatan Republik Indonesia, Pusat Data Kesehatan, Jakarta. Ekowati H, Rachmani, E.P.N and Rastuti, U. 2011.The Active fraction from Nigella sativa and Its Activity Against T47D Cell Line. Indo. J. Chem 11(3), 217 – 222. Gilani, A.H., Jabeen, Q., and Khan, M.A.U., 2004, A Review of Medicinal Uses and Pharmacological Activities of Nigella Sativa, Pakistan Journal of Biological Sciences, 7(4), 441-451. Hanahan, G., and Weinberg, R.A., 2011, The Hallmarks of Cancer, Cell, Cell Press, 100 (7), 57–70. Hassan, S.A., Ahmed, W.A., Galeb, F.M., El-Taweel, M.A., and Abu-Bedair, F.A., 2008, In Vitro Challenge using Thymoquinone on Hepatocellular Carcinoma (HepG2) Cell Line, Iranian Journal of Pharmaceutical Research, 7(4), 283-290. Ilaiyaraja, N., and Khanum, F., 2010, Nigella Sativa L. A Review Of Therapeutic Applications, Journal of Herbal Medicine and Toxicology , 4 (2), 1-8 Irawan, Hubungan Nilai AgNOR Pra Dan Pasca Kemoradiasi Dengan Respon Radiasi Pada Penderita Karsinoma Epidermoid Serviks Uteri Stadium Lanjut, Tesis, Program Pendidikan Dokter Spesialis I Obstetri Dan Ginekologi, Universitas Diponegoro, Semarang. 2008. Ivankovic, S., Stojkovic, R., Jukic, M., Milos, M., dan Jurin, M.M.M., 2006, The Antitumor Activity Of Thymoquinone And Thymohydroquinone In Vitro And In Vivo, Experimental Oncology 28, 220–224. Kubatka, P., Ahlersova E., Ahlers I., Bojkova B., Kalicka K., Adamekova E., Markova M., Chamilova M., and Cermakova M., 2002, Variability of Mammary Carsinogenesis Induction in Female Sprague-Dawley and Wistar: Han Rats : the Effect of Season and Age, Physiol. Res. , 51, 633-640 Murray, R.K., Granner, D.K., and Rodwell, V.W., 2006, Biokimia Harper. Jakarta: Penerbit Buku Kedokteran EGC. Nickavar B, Mojab F, Javidnia K, Amoli MAR. 2003Chemical composition of the fixed and volatile oils of Nigella sativa L. from Iran. Naturforsch, 58c, 629-631. Nisa, F., Hermawan, A., Murwanti, R., & Meiyanto, E. 2012. Antiproliferative effect of gynura procumbens (lour.) Merr. Leaves etanolic extract on 7,12- dimethylbenz(a)antracene induced male rat liver. Cancer. 2(1): 99-106. Rajapaksa, K.S., Sipes, I.G., and Hoyer, P.B., 2007, Involvement of Microsomal Epoxide Hydrolase Enzyme in Ovotoxicity Caused by 7,12-Dimethylbenz[a]anthracene, Toxicological Sciences, 96(2), 327- 334. Rizali and Elza, A.,2003, Teknik Pewarnaan Silver (AgNOR) Sebagai Salah Satu Cara Menentukan Aktivitas Proliferasi Sel Tumor dan Apoptosis, Jurnal Kedokteran Gigi Indonesia, 10(3),41-45. Rugo, H.S., 2006, Cancer in Current Medical Diagnosis and Treatment, 45th Edition, Eds. Tierney, Lawrence M., McPhee, Stephen J., Papadakis, Maxie A., McGraw-Hill, Publishing Company, New York, USA. Singletary, K., Macdonald, C., and Wallig, M., 1997, The Plasticizer Benzyl Butyl Phtalate (BBP) Inhibits 7,12- dimethylbenz( )anthracene (DMBA)- induced rat Mammary DNA Adduct Formation and Tumorigenesis, Carsinogenesis , 18 (8),1669-1673 Yazan, L.S., Ng. W.K., Al-Naqeeb, G., and Ismail, M., 2009, Cytotoxicity of Thymoquinone (TQ) from Nigella sativa Towards Human Cervical Carcinoma Cells (HeLa), Journal of Pharmacy Research, 2(4) , 585-589.en_US
dc.identifier.isbn978-602-18711-0-2
dc.identifier.urihttp://hdl.handle.net/11617/2342
dc.description.abstractBreast cancer is the leading cause of death in the world. Nigella sativa is one of the plants that has anticancer activity. Previous study reported Nigella sativa has cytotoxic activity in T47D cell. This study aimed at observing the effect of cloroform extract of Nigella sativa seed (NSS) on mice breast cell after initiation of 7,12-dimethylbenz [a] anthracene. Sprague Dawley strain female rats were divided into five groups. Each group consisted of 12 mice. The experiment consisted of five mice groups, corn oil solvent control group, the DMBA dose 20 mg/kgBW p.o. twice a week during five weeks, DMBA+NSS dose 250 mg/kgBW, DMBA+NSS dose 500 mg/kgBW and DMBA+NSS dose 750 mg/kgBW. Extract dissolved in corn oil was administered daily by the oral route 1 week before and during the DMBA induction. At the end of the study, mice was sacrified and breast organs were collected and stained with Haematoxylin and Eosin (H&E) and AgNOR methods. H&E staining showed that there were no histopatology changes in treated group compared with DMBA group. NSS was able to supress breast cancer cell proliferation activity. mAgNOR value on DMBA control group, dose 250, 500, 750 mg/Kg BW NSS+DMBA and corn oil were 2.14 ± 0.33; 1.47 ± 0.55; 0.83±0.24; 0.33 ± 0.23; 0.22±0.19, respectively. The results suggested that N.sativa can be develop into chemopreventive agent for breast cancer.en_US
dc.language.isoenen_US
dc.publisherMuhammadiyah University Pressen_US
dc.subjectBreast canceren_US
dc.subjectNigella sativaen_US
dc.subjectDMBAen_US
dc.subjectAntiproliferationen_US
dc.subjectAgNORen_US
dc.titleAntiproliferation Activity of Nigella Sativa on 7,12dimethylbenz[A] Antracene Induced Carcinogenesis in Female Mice Breasten_US
dc.typeArticleen_US


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