Your browser doesn't support javascript.
loading
Antiproliferative activity of Eremanthus crotonoides extracts and centratherin demonstrated in brain tumor cell lines
Lobo, Jonathas F. R.; Castro, Elaine S.; Gouvea, Dayana R.; Fernandes, Caio P.; Almeida, Fernanda B. de; Amorim, Lídia M. F. de; Burth, Patrícia; Rocha, Leandro; Santos, Marcelo G.; Harmerski, Lidilhone; Lopes, Norberto P.; Pinto, Angelo C..
Affiliation
  • Lobo, Jonathas F. R.; Universidade Federal do Rio de Janeiro. Instituto de Química. BR
  • Castro, Elaine S.; Universidade Federal do Rio de Janeiro. Instituto de Química. BR
  • Gouvea, Dayana R.; Universidade Federal do Rio de Janeiro. Instituto de Química. BR
  • Fernandes, Caio P.; Universidade Federal do Rio de Janeiro. Instituto de Química. BR
  • Almeida, Fernanda B. de; Universidade Federal do Rio de Janeiro. Instituto de Química. BR
  • Amorim, Lídia M. F. de; Universidade Federal do Rio de Janeiro. Instituto de Química. BR
  • Burth, Patrícia; Universidade Federal do Rio de Janeiro. Instituto de Química. BR
  • Rocha, Leandro; Universidade Federal do Rio de Janeiro. Instituto de Química. BR
  • Santos, Marcelo G.; Universidade Federal do Rio de Janeiro. Instituto de Química. BR
  • Harmerski, Lidilhone; Universidade Federal do Rio de Janeiro. Instituto de Química. BR
  • Lopes, Norberto P.; Universidade Federal do Rio de Janeiro. Instituto de Química. BR
  • Pinto, Angelo C.; Universidade Federal do Rio de Janeiro. Instituto de Química. BR
Rev. bras. farmacogn ; 22(6): 1295-1300, Nov.-Dec. 2012. ilus, tab
Article de En | LILACS | ID: lil-659058
Bibliothèque responsable: BR1.1
ABSTRACT
The genus Eremanthus is recognized by the predominance of sesquiterpene lactones from the furanoheliangolide type, a class of substances extensively tested against cancer cell lines. Thus, the species E. crotonoides (DC.) Sch. Bip., Asteraceae, obtained on "restinga" vegetation was evaluated against U251 and U87-MG glioma cell lines using the MTT colorimetric assay. Dichloromethane fraction was cytotoxic to both glioblastoma multiforme cell lines. We then conducted UPLC-PDA-ESI-MS/MS analysis of the dichloromethane fraction, which allowed the identification of the sesquiterpene lactones centratherin and goyazensolide. The isolation of centratherin was performed using chromatographic techniques and the identification of this substance was confirmed according to NMR data. Cytotoxic activity of centratherin alone was also evaluated against both U251 and U87-MG cells, which showed IC50 values comparable with those obtained for the commercial anticancer drug doxorubicin. All the tested samples showed cytotoxic activity against glioblastoma multiforme cells which suggests that E. crotonoides extracts may be important sources of antiproliferative substances and that the centratherin may serve as prototype for developing new antiglioblastoma drugs.
Mots clés

Texte intégral: 1 Indice: LILACS langue: En Texte intégral: Rev. bras. farmacogn Thème du journal: FARMACIA Année: 2012 Type: Article

Texte intégral: 1 Indice: LILACS langue: En Texte intégral: Rev. bras. farmacogn Thème du journal: FARMACIA Année: 2012 Type: Article