Skip to main content
Log in

Study of the cytotoxic activity of Styrax camporum extract and its chemical markers, egonol and homoegonol

  • Brief Report
  • Published:
Cytotechnology Aims and scope Submit manuscript

Abstract

The benzofuran lignans egonol and homoegonol are found in all species of the genus Styrax. Since natural products are important sources of new anticancer drugs, this study evaluated the cytotoxic activity of a hydroalcoholic extract of the stems of S. camporum (SCHE) and their chemical markers, egonol (EG) and homoegonol (HE), against different tumor cell lines (B16F10, MCF-7, HeLa, HepG2, and MO59J). A normal human cell line (GM07492A) was included. Cytotoxic activity was evaluated at different treatment times (24, 48 and 72 h) using the XTT assay. More effective results were observed after 72 h of treatment. The lowest IC50 values were found for the HepG2 cell line, ranging from 11.2 to 55.0 µg/mL. The combination of EG and HE exerted higher cytotoxic activity than SCHE or treatment with either lignan alone, with the lowest IC50 (13.31 µg/mL) being observed for the MCF-7 line. Furthermore, treatment with these lignans was significantly more cytotoxic for some tumor cell lines compared to the normal cell line, GM07492A, indicating selectivity. These results suggest that these lignans may be used to treat cancer without affecting normal cells.

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

References

  • Bacchi EM, Sertié JA (1994) Antiulcer action of Styrax camporum and Caesalpinia ferrea in rats. Planta Med 60:118–120

    Article  CAS  Google Scholar 

  • Bacchi EM, Sertié JA, Villa N, Katz H (1995) Antiulcer action and toxicity of Styrax camporum and Caesalpinia ferrea. Planta Med 61:204–207

    Article  CAS  Google Scholar 

  • Braguini CG, Bertanha CS, Gonçalves UO, Magalhães LG, Rodrigues V, Melleiro-Gimenez VM, Groppo M, Silva ML, Cunha WR, Januário AH, Pauletti PM (2012) Schistosomicidal evaluation of flavonoids from two species of Styrax against Schistosoma mansoni adult worms. Pharma Biol 50:925–929

    Article  Google Scholar 

  • Hayakawa I, Shioya R, Agatsuma T, Furukawa H, Sugano Y (2004) Thienopyridine and benzofuran derivatives as potent anti-tumor agents possessing different structure-activity relationships. Bioorg Med Chem Lett 14:3411–3414

    Article  CAS  Google Scholar 

  • Li QL, Li BG, Qi HY, Gao XP, Zhang GL (2005) Four new benzofurans from seeds of Styrax perkinsiae. Planta Med 71:847–851

    Article  CAS  Google Scholar 

  • Lorenzi H (1982) Árvore Brasileiras. Manual de identificação e cultivo de plantas arbóreas nativas do Brasil. Nova Odessa Plantarum, São Paulo

    Google Scholar 

  • Min BS, Oh SR, Ahn KS, Kim JH, Lee J, Kim DY, Kim EH, Lee HK (2004) Anti-complement activity of norlignans and terpenes from the stem bark of Styrax japonica. Planta Med 70:1210–1215

    Article  CAS  Google Scholar 

  • Moraes AC, Bertanha CS, Gimenez VM, Groppo M, Silva ML, Cunha WR, Januário AH, Pauletti PM (2011) Development and validation of a high-performance liquid chromatography method for quantification of egonol and homoegonol in Styrax species. Biomed Chromatogr 26:869–874

    Article  Google Scholar 

  • Nussbaumer S, Bonnabry P, Veuthey JL, Fleury-Souverain S (2011) Analysis of anticancer drugs: a review. Talanta 85:2265–2289

    Article  CAS  Google Scholar 

  • Pan MH, Ho CT (2008) Chemopreventive effects of natural dietary compounds on cancer development. Chem Soc Rev 37:2558–2574

    Article  CAS  Google Scholar 

  • Pauletti PM, Araújo AR, Young MCM, Giesbrecht AM, Bolzani VS (2000) Nor-lignanas from the leaves of Styrax ferrugineus (Styracaceae) with antibacterial and antifungical activity. Phytochemistry 5:597–601

    Article  Google Scholar 

  • Reiter C, Capcl Karagöz A, Fröhlich T, Klein V, Zeino M, Viertel K, Held J, Mordmüller B, Emirdağ Öztürk S, Anıl H, Efferth T, Tsogoeva SB (2014) Synthesis and study of cytotoxic activity of 1,2,4-trioxane-and egonol-derived hybrid molecules against Plasmodium falciparum and a multidrug-resistent human leukemia cells. Eur J Med Chem 75:403–412

    Article  CAS  Google Scholar 

  • Salvador JA, Carvalho JF, Neves MA, Silvestre SM, Leitão AJ, Silva MM, Sá e Melo ML (2013) Anticancer steroids: linking natural and semi-synthetic compounds. Nat Prod Rep 30:324–374

    Article  CAS  Google Scholar 

  • Suffness M, Pezzuto JM (1990) Assays related to cancer drug discovery. In: Hostettmann K (ed) Methods in plant biochemistry: assay for bioactivity. Academic Press, London, pp 71–133

    Google Scholar 

  • Teles HL, Hemerly JP, Paulettit PM, Pandolfi JR, Araujot AR, Valentini SR, Young MC, Bolzani VS, Silva DH (2005) Cytotoxic lignans from the stems of Styrax camporum (Styracaceae). Nat Prod Res 14:319–323

    Article  Google Scholar 

Download references

Acknowledgments

This work was supported by the São Paulo Research Foundation (FAPESP; Brazil; Grant # 2013/13903-9). P.F. Oliveira was the recipient of a Doctoral fellowship from FAPESP (Grant # 2011/201310-2). The authors are grateful to Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for the fellowships granted.

Conflict of interest

The authors declared that they have no conflicts of interest.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Pollyanna Francielli de Oliveira.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

de Oliveira, P.F., Damasceno, J.L., Bertanha, C.S. et al. Study of the cytotoxic activity of Styrax camporum extract and its chemical markers, egonol and homoegonol. Cytotechnology 68, 1597–1602 (2016). https://doi.org/10.1007/s10616-015-9864-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10616-015-9864-y

Keywords

Navigation