Officinalis Chaix pada IC

Selain itu, monoterpen juga memiliki aktivitas molekuler yang berpotensi untuk mendasari index terapetik yang positif, pada penelitian Gould 1997 dikatakan bahwa monoterpen mampu menghambat isoprenilasi small G protein, isoprenilasi protein memegang peranan penting dalam fungsionalisasi protein yang mampu memacu terjadinya kanker McTaggart, 2006. Penghambatan ini dapat mengubah sinyal transduksi dan mengakibatkan ekspresi gen yang berubah, hasil dari ekspresi gen yang baru telah diidentifikasi mampu menurunkan regresi dari karsinoma kelenjar payudara. 47

BAB V KESIMPULAN DAN SARAN

A. Kesimpulan

Ekstrak etanol daun lavender mempunyai efek sitotoksik pada sel kanker payudara T47D serta menginduksi apoptosis dengan nilai IC 50 sebesar 232,86 µgmL dan mampu menekan ekspresi protein ERα.

B. Saran

1. Perlu dilakukan proses pengujian lebih lanjut untuk mengetahui senyawa- senyawa yang terkandung di dalam ekstrak etanol daun L. officinalis Chaix. 2. Potensi ketoksikan dari ekstrak etanol daun L. officinalis Chaix perlu ditingkatkan dengan mengujikannya pada model sel kanker payudara lain. 3. Penelitian dilanjutkan dengan membuat suatu formulasi sediaan menggunakan ekstrak etanol daun Lavandula officinalis Chaix sebagai obat kemopreventif. DAFTAR PUSTAKA Adjo, J., dan Lin, S., 2012, Comparison of Functional Proteomic Analyses of Human Breast Cancer Cell Lines T47D and MCF7, Plos One, 72, 1-4. Alberts, B. dkk.. 1994. Molecular Biology of the Cell. Garland Publishing, New York, 186-188. American Type Culture Collection, 2011, MTT Cell Proliferation Assay, University Boulevard, www.atcc.org, diakses tanggal 20 Februari 2015. Bardon, S., Picard, K., dan Martel, P., 2002, Monoterpene Inhibit Cell Growth, Cell Cycle Progession, and Cyclin D1 Gene Expression in Human Breast Cancer Cell Lines, Nutrition and Cancer, 321, 1-7. Chu, C., dan Kemper, K., 2001, Lavender Longwood Herbal Task Force, http:www.mcp.eduherbal, diakses tanggal 12 Desember 2014. Compston, J., 2001, Sex Steroids and Bone, APS, 811, 429. Crowell, P., 1997, Monoterpenes in Breast Cancer Chemopreventive, Breast Cancer Research anf Treatment, 46, 191- 197. Deroo, B., dan Korach, K., 2006, Estrogen Receptors and Human Disease, JCI, 116 3. Darinus, O., 2002, Aplikasi software R dalam analisis regressi, Fakultas Matematika dan Ilmu Pengetahuan Alam, Universitas Sumatera Utara. Devi, U., 1989, Basics of Carcinogenesis, Health Administrator, 17 1, 16- 24. Doyle, A., dan Griffiths J.B., 2000, Cell and Tissue Culture: Laboratory Procedures in Biotechnology, John Willey Sons LTD, New York, 62- 64. European Medicines Agency, 2011, Assessment report on Lavandula angustifolia Mill., aetheroleum and Lavandula angustifolia Mill., flos, HMPC,16d1. Gould, M., 1997, Cancer Chemoprevention and Therapy by Monoterpenes, Enviromental Health Perspectives, 105 4, 977- 979. Hajhashemi, V., Ghannadi, A., dan Sharif, B., 2003, Anti-inflammatory and analgesic properties of the leaf extracts and essential oil of Lavandula angustifolia Mill., Journal of Ethnopharmacology, 892003, pp. 67- 71. Handayani, S., 2012, Selaginella Active Fractions Induce Apoptosis On T47d Breast Cancer Cell, Indonesian J. Pharm., 231, 48-50. A Hayashi dkk., 2003, The Expression and Function of Estrogen Receptor α and β in Human Breast Cancer and its Clinical Application, Endocrine- Realted Cancer, 10, 193- 202. Hondermarck, H., 2003, Breast Cancer : When Proteomics Challenges Biological Complexity, Molecular and Proteomics, 2, 281- 291. Istvan, V., Haanen, C., Nakken, H., dan Reutelingsperger, C., 1995, A novel assay for apoptosis Flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein labelled Annexin V, Journal of Immunological Methods, 1, 184. Javois, L., 1999, Immunocytochemical Methods and Protocol 2 nd Ed., Humana Press, USA, 3-10. Johnson, A., dkk., 2002, Molecular Biology of the Cell. 4th edition, Garland Science, New York, 335. Kamuhabwa, A., Nshimo, C., dan de Witte P., 2000, Cytotoxicity of some medicinal plant extracts used in Tanzanian traditional medicine, J. Ethnopharmacol, 702, 143- 149. Karolina, H., dkk., 2010, R Molecular subtypes of breast cancer are associated with characteristic DNA methylation patterns, CBR, 12, 1- 16. Kementrian Kesehatan Republik Indonesia, 2014, Hilangkan Mitos tentang Kanker, http:www.depkes.go.idarticleprint201407070001hilangkan- mitos-tentang-kanker.html, diakses tanggal 10 Mei 2014. Lim, T., 2014, Lavandula angustifolia, Edible Medicinal and Non Medicinal Plant, 8, 165-167. Liston, B., dkk., 2003, Perillyl Alcohol as Chemopreventive Agent in N- Nitrosomethylbenzylamine-induced Rat Esophageal Tumorigenesis, American Association for Cancer Research, 2399-2403. Lumongga, F., 2008, Apoptosis, Departemen Patologi Anatomi Fakultas Kedokteran Universitas Sumatera Utara, Medan, 2-4. Macey, M., 2007, Flow cytometry: Principles and Applications, Springer Science Business Media, Totowa, pp. 1-2. Machana, S., Weerapreeyakul, N., Barusrux, S., Nonpunya, A., Sripanidkulchai, B., Thitimetharoch, T., 2011, Cytotoxic and apoptotic effects of six herbal plants against the human hepatocarcinoma HepG2 cell line, Chin Med.,61, 1-8. McTaggart, S., 2006, Isoprenylated Protein, Cell. Mol. Life. Sci, 63, 255- 267. Mann, M., Cortez, V., and Vadlamudi, K., 2011, Epigenetics of Estrogen Receptor Signaling: Role in Hormonal Cancer Progression and Therapy, Cancers, 3, 1691- 1699. National Cancer Institue, 2013, Breast Cancer Treatment, http:www.cancer.govcancertopicspdqtreatmentbreastPatientpage1. Diakses tanggal 1 juli 2014. Neumann, B., dan Rossi, M., 2012, Effects of Exemestane on Two-Dimensional and Three-Dimensional T47D Breast Cancer Cell Cultures, University of New Haven Summer Undergraduate Research Fellowship 2012, 1-4. Nevein, M., Gamil, M., dan Nagi, F., 2014, Phytochemical Studies and In Vivo Antioxidant Activity of Two Lavandula Species Lamiaceae Against Streptozotocin Induced Oxidative Stress in Albino Rats, JBPR, 43, 30-40. Hurzijah, I., Putri, D., Rivanti, E., dan Meiyanto, E., 2012, Secang Caesalpinia sappan L. Heartwood Ethanolic Extract Shows Activity as Doxorubicin Co-chemotherapeutic Agent by Apoptosis Induction on T47D Breast Cancer Cells, ISCC, 32, 377-384. Osborne, K., 1998, Tamoxifen in the Treatment of Breast Cancer, The New England Journal of Medicine, 33922, 1609-1912. 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