Inhibitory Effects of Brazilian Propolis on Tumor Promotion in Two-Stage Mouse Skin Carcinogenesis
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Keywords

 Propolis, moronic acid, cancer chemoprevention, tumor promotion, two-stage carcinogenesis

How to Cite

Ken Yasukawa, So Yeon Yu, Shigetoshi Tsutsumi, Masahiko Kurokawa, & Yong K. Park. (2012). Inhibitory Effects of Brazilian Propolis on Tumor Promotion in Two-Stage Mouse Skin Carcinogenesis. Journal of Pharmacy and Nutrition Sciences, 2(1), 71–76. https://doi.org/10.6000/1927-5951.2012.02.01.10

Abstract

Propolis is produced by honeybees and has many biological properties, including immunomodulatory, anti-inflammatory, anti-oxidant, anti-bacterial, anti-viral and anti-cancer actions. Five ethanol extracts of Brazilian propolis were tested for inhibition of 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced inflammation in mice. The ethanol extract of Brazilian propolis AF-08 markedly inhibited TPA-induced inflammatory ear edema in mice. This extract suppressed tumor promotion by TPA following initiation with 7,12-dimethylbenz[a]anthracene (DMBA) in mouse skin. Moronic acid, a major component of Brazilian propolis AF-08, markedly inhibited two-stage carcinogenesis by DMBA plus TPA. These results suggest that Brazilian propolis AF-08 contributes to the prevention of cancer.

https://doi.org/10.6000/1927-5951.2012.02.01.10
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References

Kawabe M, Lin C, Kimoto N, Sano M, Hirose M, Shirai T. Modifying effects of propolis on MeIQx promotion of rat hepatocarcinogenesis and in a female rat two-stage carcinogenesis model after multiple carcinogen initiation. Nutr Cancer 2000; 37: 179-86. http://www.tandfonline.com/doi/abs/10.1207/S15327914NC372_10?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%3dpubmed

Akihisa T, Nakamura Y, Tagata M, et al. Anti-inflammatory and anti-tumor-promoting effects of triterpene acids and sterols from the fungus Ganoderma lucidum. Chem Biodiv 2007; 4: 224-31. http://onlinelibrary.wiley.com/doi/10.1002/cbdv.200790027/abstract

Yasukawa K, Takahashi H, Kitanaka S, Hirayama H, Shigemoto K. Inhibitory effect of an aqueous extract of Phellinus linteus on tumor promotion in mouse skin. Mushroom Sci Biotechnol 2007; 15: 97-101.

Yasukawa K, Sun Y, Kitanaka S, Tomizawa N, Miura M, Motohashi S. Inhibitory effect of the Rhizomes of Alpinia officinarum on TPA-induced inflammation and tumor promotion in two-stage carcinogenesis in mouse skin. J Nat Med 2008; 62: 374-8. http://www.springerlink.com/content/8665840m5687n561/?MUD=MP

Yasukawa K, Akihisa T, Kanno H, et al. Inhibitory effects of sterols isolated from Chlorella vulgaris on 12-O-tetradecanoyl- phorbol-13-acetate-induced inflammtion and tumor promotion in mouse skin. Biol Pharm Bull 1996; 19: 573-6.

Banskota AH, Tezuka Y, Kadota S. Recent progress in pharmacological research of propolis. Phytother Res 2001; 15: 561-71. http://onlinelibrary.wiley.com/doi/10.1002/ptr.1029/abstract

Sforcin JM. Propolis and the immune system: a review. J Ethonopharmacol 2007; 113: 1-14. http://www.sciencedirect.com/science/article/pii/S0378874107002474

Watanabe MAE, Amarante MK, Conti BJ, Sforcin JM. Cytotoxic constituents of propolis including anticancer effects: a review. J Pharm Pharmacol 2011; 63: 1378-86. http://onlinelibrary.wiley.com/doi/10.1111/j.2042-7158.2011.01331.x/abstract

Simon-Finstrom M, Spivak M. Propolis and bee health: the natural history and significance of resin use by honey bees. Apidologie 2010; 41: 295-311. http://www.springerlink.com/content/t3umq4l75810611w/

Ito J, Chang F-R, Wang H-K, et al. Anti-AIDS agents. 48. Anti-HIV activity of moronic acid derivatives and the new melliferone-related triterpenoid isolated from Brazilian propolis. J Nat Prod 2001; 64: 1278-81. http://pubs.acs.org/doi/abs/10.1021/np010211x

Ghisalberti EL. Propolis: a review. Bee World 1979; 60: 59-84.

Burdock GA. Review of the biological properties and toxicity of bee propolis (propolis). Food Chem Toxicol 1998; 36: 347-363. http://www.sciencedirect.com/science/article/pii/S0278691597001452

Viuda-Martos M, Ruiz-Navajas Y, Fernández-López J, Pérez-Álvarez JA. Functional properties of honey, propolis, and royal jelly. J Food Sci 2008; 73: 117-24. http://onlinelibrary.wiley.com/doi/10.1111/j.1750-3841.2008.00966.x/abstract

Park YK, Alencar SM, Aguiar CL. Botanical origin and chemical composition of Brazilian propolis. J Agric Food Chem 2002; 50: 2502-6. http://pubs.acs.org/doi/abs/10.1021/jf011432b

Isla MI, Paredes-Guzman JF, Nieva-Moreno MI, Koo H, Park YK. Some chemical composition and biological activity of northern Argentine propolis. J Agric Food Chem 2005; 53: 4466-72. http://pubs.acs.org/doi/abs/10.1021/jf040130h

Yasukawa K, Takido M, Takeuchi M, Nakagawa S. Effect of chemical constituents from plants on 12-O-tetradecanoylphorbol-13-acetate- induced inflammation in mice. Chem Pharm Bull (Tokyo) 1989; 37: 1071-3.

Akihisa T, Yasukawa K. Antitumor-promoting and anti-inflammatory activities of triterpenoids and sterols from plants and fungi. In: Attu-ur-Rahman, editor. Studies in natural products chemistry, Vol. 25, Bioactive natural products (Part F), Amsterdam, Elsevier Science Ltd. 2001; pp. 43-87.

Yasukawa K. Cancer chemopreventive agents: natural pentacyclic triterpenoids. In: Salvador JAR, editor. Pentacyclic triterpenes as promising agents in cancer. New York: Nova Science Publishers, Inc. 2010; pp. 127-57. https://www.novapublishers.com/catalog/product_info.php?products_id=20014

Shimizu T, Hino A, Tsutsumi A, Park YK, Watanabe W, Kurokawa M. Anti-influenza virus activity of propolis in vitro and its efficacy against influenza infection in mice. Antiviral Chem Chemothr 2008; 19: 7-13. http://www.intmedpress.com/journals/avcc/abstract.cfm?id=221&pid=92

Shimizu T, Takeshita Y, Takamori Y, et al. Efficacy of Brazilian Propolis againstHerpes Simplex Virus Type 1 Infection inMice and TheirModes of Antiherpetic Efficacies. Evid-Based Complement and Alternat Med 2011; 2011: 976196. http://www.hindawi.com/journals/ecam/2011/976196/

Kurokawa M, Basnet P, Ohsugi M, et al. Anti-herpes simplex virus activity of moronic acid purified from Rhus javanica in vitro and in vivo. J Pharmacol Exp Thert 1999; 289: 72-8. http://jpet.aspetjournals.org/content/289/1/72.long

Yu D, Sakurai Y, Chen CH, et al. Anti-AIDS agents 69. Moronic acid and other triterpene derivatives as novel potent anti-HIV agents. J Med Chem 2006; 49: 5462-9. http://pubs.acs.org/doi/abs/10.1021/jm0601912

Qian K, Kuo RY, Chen CH, Huang L, Morris-Natschke SL, Lee KH. Anti-AIDS agents 81. Design, synthesis, and structure-activity relationship study of betulinic acid and moronic acid derivatives as potent HIV maturation inhibitors. J Med Chem 2010; 53: 3133-41. http://pubs.acs.org/doi/abs/10.1021/jm901782m

Chang F-R, Hsieh Y-C, Chang Y-F, Lee K-H, Wu Y-C, Chang L-K. Inhibition of the Epstein-Barr virus lytic cycle by moronic acid. Antiviral Res 2010; 85: 490-5. http://www.sciencedirect.com/science/article/pii/S0166354209005415

Inada A, Somekawa M, Murata H, et al. Phytochemical studies on meliaceous plants. VIII. Structures and inhibitory effects on Epstein-Barr virus activation of triterpenoids from leaves of Chisocheton macrophyllus King. Chem Pharm Bull 1993; 41: 617-9.

Rios MY, Salina D, Villarreal ML. Cytotoxic activity of moronic acid and identification of the new triterpene 3,4-seco-olean-18-ene-3,28-dioic acid from Phoradendron reichenbachianum. Planta Med 2001; 67: 443-6. https://www.thieme-connect.com/DOI/DOI?10.1055/s-2001-15823

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Copyright (c) 2012 Ken Yasukawa, So Yeon Yu, Shigetoshi Tsutsumi, Masahiko Kurokawa , Yong K. Park