Skip to main content
Log in

Anticarcinogenic compounds in the Uzbek medicinal plant, Helichrysum maracandicum

  • Original Paper
  • Published:
Journal of Natural Medicines Aims and scope Submit manuscript

Abstract

An ethanol extract of Helichrysum maracandicum showed antiproliferative activity against cultured cells of SENCAR mouse in an in vitro assay, and activity-guided fractionation of the extract resulted in the isolation of isosalipurposide as an active substance. Naringenin chalcone, the aglycone of isosalipurposide, also showed strong antiproliferative activity. An in vivo assay of two-stage carcinogenesis on mouse skin revealed that epidermal application of isosalipurposide resulted in delayed formation of papillomas. Western blot analysis showed that the expression of p38 mitogen-activated protein kinase was suppressed by the administration of naringenin chalcone or isosalipurposide, which might be related to the anticarcinogenic activity.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. Murakami A, Ohigashi H, Koshimizu K (1996) Anti-tumor promotion with food phytochemicals: a strategy for cancer chemoprevention. Biosci Biotechnol Biochem 60:1–8

    Article  PubMed  CAS  Google Scholar 

  2. Digiovanni J (1992) Multistage carcinogenesis in mouse skin. Pharmacol Ther 54:63–128

    Article  PubMed  CAS  Google Scholar 

  3. Bode AM, Dong Z (2000) Signal transduction pathways: targets for chemoprevention of skin cancer. Lancet Oncol 1:181–188

    Article  PubMed  CAS  Google Scholar 

  4. Suzgec S, Mericli AH, Houghton PJ, Cubukcu B (2005) Flavonoids of Helichrysum compactum and their antioxidant and antibacterial activity. Fitoterapia 76:269–272

    Article  PubMed  CAS  Google Scholar 

  5. Delapuerta R, Saenz MT, Garcia MD (1993) Choleretic effect of the essential oil from Helichrysum picardii Boiss and Reuter in rats. Phytother Res 7:376–377

    Article  CAS  Google Scholar 

  6. Drewes SE, Mudau KE, Van Vuuren SF, Viljoen AM (2006) Antimicrobial monomeric and dimeric diterpenes from the leaves of Helichrysum tenax var tenax. Phytochemistry 67:716–722

    Article  PubMed  CAS  Google Scholar 

  7. Jakupovic J, Kuhnke J, Schuster A, Metwally MA, Bohlmann F (1986) Phloroglucinol derivatives and other constituents from South African Helichrysum species. Phytochemistry 25:1133–1142

    Article  CAS  Google Scholar 

  8. Randriaminahy M, Proksch P, Witte L, Wray V (1992) Lipophilic phenolic constituents from Helichrysum species endemic to Madagascar. Z Naturforsch C 47:10–16

    CAS  Google Scholar 

  9. Meyer JJM, Afolayan AJ (1995) Antibacterial activity of Helichrysum aureonitens (Asteraceae). J Ethnopharmacol 47:109–111

    Article  PubMed  CAS  Google Scholar 

  10. Tepe B, Sokmen M, Akpulat HA, Sokmen A (2005) In vitro antioxidant activities of the methanol extracts of four Helichrysum species from Turkey. Food Chem 90:685–689

    Article  CAS  Google Scholar 

  11. Jager AK, Hutchings A, vanStaden J (1996) Screening of Zulu medicinal plants for prostaglandin-synthesis inhibitors. J Ethnopharmacol 52:95–100

    Article  PubMed  CAS  Google Scholar 

  12. Musabayane CT, Munjeri O, Mdege ND (2003) Effects of Helichrysum ceres extracts on renal function and blood pressure in the rat. Ren Fail 25:5–14

    Article  PubMed  CAS  Google Scholar 

  13. Tokuda H, Ichiishi E, Onozuka M, Yamaguchi S, Konoshima T, Takasaki M, Nishino H (1998) The tumor initiating activity of NO donor. In: Moncada S, Tada N, Maeda H (eds) Biology of nitric oxide, part 6. Portland Press, London, pp 185–186

    Google Scholar 

  14. Zapesochnaya GG, Kurkin VA, Braslavskii VB, Filatova NV (2002) Phenolic compounds of Salix acutifolia bark. Chem Nat Comp 38:314–318

    Article  CAS  Google Scholar 

  15. Le Bail JC, Pouget C, Fagnere C, Basly JP, Chulia AJ, Habrioux G (2001) Chalcones are potent inhibitors of aromatase and 17β-hydroxysteroid dehydrogenase activities. Life Sci 68:751–761

    Article  PubMed  CAS  Google Scholar 

  16. Kato R, Nakadate T, Yamamoto S, Sugimura T (1983) Inhibition of 12-O-tetradecanoylphorbol-13-acetate-induced tumor promotion and ornithine decarboxylase activity by quercetin: possible involvement of lipoxygenase inhibition. Carcinogenesis 4:1301–1305

    Article  PubMed  CAS  Google Scholar 

  17. Facino RM, Carini M, Franzoi L, Pirola O, Bosisio E (1990) Phytochemical characterization and radical scavenger activity of flavonoids from Helichrysum italicum G. Don (Compositae). Pharmacol Res 22:709–721

    Article  PubMed  CAS  Google Scholar 

  18. Calliste CA, Le Bail JC, Trouillas P, Pouget C, Habrioux G, Chulia AJ, Duroux JL (2001) Chalcones: structural requirements for antioxidant, estrogenic and antiproliferative activities. Anticancer Res 21:3949–3956

    PubMed  CAS  Google Scholar 

  19. Mantena SK, Katiyar SK (2006) Grape seed proanthocyanidins inhibit UV-radiation-induced oxidative stress and activation of MAPK and NF-κB signaling in human epidermal keratinocytes. Free Radic Biol Med 40:1603–1614

    Article  PubMed  CAS  Google Scholar 

  20. Katiyar SK, Afaq F, Azizuddin K, Mukhtar H (2001) Inhibition of UVB-induced oxidative stress-mediated phosphorylation of mitogen-activated protein kinase signaling pathways in cultured human epidermal keratinocytes by green tea polyphenol (−)-epigallocatechin-3-gallate. Toxicol Appl Pharmacol 176:110–117

    Article  PubMed  CAS  Google Scholar 

  21. Chen WX, Tang QB, Gonzales MS, Bowden GT (2001) Role of p38 MAP kinases and ERK in mediating ultraviolet-B induced cyclooxygenase-2 gene expression in human keratinocytes. Oncogene 20:3921–3926

    Article  PubMed  CAS  Google Scholar 

  22. Subbaramaiah K, Dannenberg AJ (2003) Cyclooxygenase 2: a molecular target for cancer prevention and treatment. Trends Pharmacol Sci 24:96–102

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Michiho Ito.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Yagura, T., Motomiya, T., Ito, M. et al. Anticarcinogenic compounds in the Uzbek medicinal plant, Helichrysum maracandicum . J Nat Med 62, 174–178 (2008). https://doi.org/10.1007/s11418-007-0223-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11418-007-0223-y

Keywords

Navigation