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Extracts of Centaurea bornmuelleri and Centaurea huber-morathii inhibit the growth of colon cancer cells in vitro

  • Sarker, Satyajit Dey (School of Biomedical Sciences, University of Ulster at Coleraine) ;
  • Shoeb, Mohammad (School of Pharmacy, The Robert Gordon University) ;
  • Celik, Sezgin (Department of Biology, Faculty of Science and Literature, Canakkale Onsekiz Mart University) ;
  • Jaspars, Marcel (Marine Natural Products Laboratory, Department of Chemistry, University of Aberdeen) ;
  • Nahar, Lutfun (School of Life Sciences, The Robert Gordon University) ;
  • Kong-Thoo-Lin, Paul (School of Life Sciences, The Robert Gordon University) ;
  • MacManus, Stephen M (School of Pharmacy, The Robert Gordon University)
  • Published : 2007.12.31

Abstract

Plants from the genus Centaurea (C.) (Family: Asteraceae alt. Compositae), widely distributed in Asia, Europe and North America, have traditionally been used in the treatment of various ailments. As a part of our on-going studies on the plants from the genus C. for their phytochemistry and biological activities, extracts of the seeds of Turkish endemic C. species, C. bornmuelleri and C. huber-morathii, were tested for their cytotoxicity towards the CaCo2 colon cancer cell line as well as for the toxicity towards the brine shrimps, using the MTT and the brine shrimp lethality assays, respectively. Among the extracts, the MeOH extract of these plants showed significant toxicity towards the brine shrimps ($LD_{50}=55.2{\times}10^{-2}\;and\;42.4{\times}10^{-2}mg/ml$, respectively). The MeOH extract of both C. species also inhibited the growth of CaCo2 colon cancer cells in the MTT assay ($IC_{50}$=29.9 and 33.0 g/ml, respectively). As the most prominent activities in both assays were observed with the MeOH extracts, it can be assumed that the compound(s) responsible for these activities are polar in nature.

Keywords

References

  1. Clapham AR, Tutin TG, Warburg EF. (1952) Flora of the British Isles. Cambridge University Press, UK
  2. Cooper G, Laird A, Nahar L, Sarker SD. (2002) Lignan glucosides from the seeds of Centaurea americana (Compositae). Biochem. Syst. Ecol. 30, 65-67 https://doi.org/10.1016/S0305-1978(01)00062-X
  3. Ferrigni NR, McLaughlin JL, Powell RG, Smith CR Jr. (1984) Use of Potato Disc and Brine Shrimp Bioassay to detect activity and isolate piceatannol as the antileukemic principles from the Seeds of Euphorbia lagascae. J. Nat. Prod. 47, 347-352 https://doi.org/10.1021/np50032a019
  4. Finney DJ. (1971). Probit Analysis, 3rd edn, Cambridge University Press, Cambridge
  5. Ferguson CA, Nahar L, Finnie D, Kumarasamy Y, Reid R, Mir-Babayev NF, Sarker SD. (2003) Centaurea scabiosa: A source of dibenzylbutyrolactone lignans. Biochem. Syst. Ecol. 31, 303-305 https://doi.org/10.1016/S0305-1978(02)00143-6
  6. Grieve M. (2002) A Modern Herbal. Available on-line athttp:// botanical.com/botanical/mgmh/c/centau46.html
  7. GRIN database. (2006) USDA, ARS, National Genetic Resources Program, Germplasm Resources Information Network - (GRIN), National Germplasm Resources Laboratory, Beltsville, Maryland, USA. Available on-line at: http://www.ars-grin.gov/cgi-bin/npgs/ html/genus.pl?2232
  8. Kumarasamy Y, Nahar L, Cox PJ, Dinan LN, Ferguson CA, Finnie D, Jaspars M, Sarker SD. (2003a) Biological activities of lignans from Centaurea scabiosa. Pharm. Biol. 41, 203-206 https://doi.org/10.1076/phbi.41.3.203.15099
  9. Kumarasamy Y, Middleton M, Nahar L, Sarker SD. (2003b) Bioactivity of indole alkaloids from the seeds of Centaurea nigra. Fitoterapia 74, 609-612
  10. Kumarasamy Y, Fergusson M, Nahar L, Sarker SD. (2002) Biological activity of moschamindole from Centaurea moschata. Pharm. Biol. 40, 307-310 https://doi.org/10.1076/phbi.40.4.307.8467
  11. McLaughlin JL. (1991) Crown gall tumours on potato discs and brine shrimp lethality: two simple bioassyas, for higher plant screening and fractionation. In: Hostettman, K., editor. Methods in plant biochemistry, Academic Press, London
  12. Middleton M, Cox PJ, Jaspars M, Kumarasamy Y, Nahar L, Reid R, Sarker SD. (2003) Dibenzylbutyrolactone lignans and indole alkaloids from the seeds of Centaurea nigra. Biochem. Syst. Ecol. 31, 653- 656 https://doi.org/10.1016/S0305-1978(02)00227-2
  13. Meyer BN, Ferrigni RN, Putnam JE, Jacobsen LB, Nichols DE, Mclaughlin JL. (1982) Brine shrimp: a convenient bioassay for active plant constituents. Planta Med. 45, 31-34 https://doi.org/10.1055/s-2007-971236
  14. Mossman T. (1983) Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 65, 55?63 https://doi.org/10.1016/0022-1759(83)90303-4
  15. Phytochemical and Ethnobotanical databases. (2006) USDA, ARS, Beltsville Agricultural Research Center, Beltsville, Maryland, USA. Available on-line at: http://www.ars-grin.gov/cgi-bin/duke/ethnobot.pl
  16. Ribeiro NL, Nahar L, Kumarasamy Y, Mir-Babayev N, Sarker SD. (2002) Flavonoid C-glucosides and a lignan from Centaurea macrocephala (Compositae). Biochem. Syst. Ecol. 30, 1097-1100 https://doi.org/10.1016/S0305-1978(02)00046-7
  17. Sarker SD, Kumarasamy Y, Shoeb M, Celik S, Eucel E, Middleton M, Nahar L. (2005) Antibacterial and antioxidant activities of three Turkish species of the genus Centaurea, Orient. Pharm. Exp. Med. 5, 246-250
  18. Sarker SD, Laird A, Nahar L, Kumarasamy Y, Jaspars M. (2001) Indole alkaloids from the seeds of Centaurea cyanus (Asteraceae). Phytochemistry 57, 1273-1276 https://doi.org/10.1016/S0031-9422(01)00084-X
  19. Sarker SD, Dinan L, Sik V, Underwood E, Waterman PG. (1998a) Moschamide: an unusual alkaloid from the seeds of Centaurea moschata. Tetrahedron Lett. 39, 1421-1424 https://doi.org/10.1016/S0040-4039(97)10818-8
  20. Sarker SD, Sik V, Dinan L, Rees HH. (1998b) Moschatine: An unusual steroidal glycoside from Centaurea moschata. Phytochemistry 48, 1039-1043 https://doi.org/10.1016/S0031-9422(97)01038-8
  21. Sarker SD, Girault J-P, Lafont R, Dinan, L. (1998c) (20R) 15$\alpha$-Hydroxy-$\beta$,9$\alpha$,14$\alpha$,17$\alpha$-pregn-4-en-3-one 20-O-$\beta$-D-glucopyranoside from Centaurea moschata. Pharm. Biol. 36, 202-206 https://doi.org/10.1076/phbi.36.3.202.6346
  22. Sarker SD, Savchenko T, Whiting P, Sik V, Dinan LN. (1997a) Moschamine, cis-moschamine, moschamindole and moschamindolol: four novel indole alkaloids from Centaurea moschata. Nat. Prod. Lett. 9, 189-199
  23. Sarker SD, Savchenko T, Whiting P, Sik V, Lafont R, Dinan L. (1997) Occurrence of ecdysteroids in the genus Centaurea: 20-hydroxy ecdysone from Centaurea moschata. Biochem. Syst. Ecol. 25, 367-368 https://doi.org/10.1016/S0305-1978(97)00018-5
  24. Shoeb M, Rahman MM, Nahar L, Jaspars M, MacManus S, Delazar A and Sarker SD. (2004a) Bioactive lignans from the seeds of Centaurea macrocephala. DARU 12, 87-93
  25. Shoeb M, Jaspars M, MacManus SM, Majinda RRT, Sarker SD. (2004b) Epoxylignans from the seeds of Centaurea cyanus. Biochem. Syst. Ecol. 32, 1201-1204 https://doi.org/10.1016/j.bse.2004.03.011
  26. Shoeb M, Celik S, Jaspar M, Kumarasamy Y, MacManus SM, Nahar L, Thoo-Lin PK, Sarker SD. (2005) Isolation, structure elucidation and bioactivity of schischkiniin, a unique indole alkaloid from the seeds of Centaurea schischkini.Tetrahedron 61, 9001-9006 https://doi.org/10.1016/j.tet.2005.07.047
  27. Shoeb M, MacManus SM, Jaspars M, Trevidadu J, Nahar L, Kong-Thoo-Lin P, Sarker SD. (2006) Montamine, a unique dimeric indole alkaloid, from the seeds of Centaurea montana (Asteraceae), and its in vitro cytotoxic activity against the CaCo2 colon cancer cells, Tetrahedron (in press)

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