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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Cytotoxicity and genotoxicity of coronaridine from Tabernaemontana catharinensis A.DC in a human laryngeal epithelial carcinoma cell line (Hep-2)

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Author(s):
Rizo, Walace Fraga [1] ; Ferreira, Luis Eduardo [1] ; Colnaghi, Vanessa [1] ; Martins, Juliana Simoes [1] ; Franchi, Leonardo Pereira [2] ; Takahashi, Catarina Satie [2] ; Beleboni, Rene Oliveira [1] ; Marins, Mozart [1] ; Pereira, Paulo Sergio [1] ; Fachin, Ana Lucia [1]
Total Authors: 10
Affiliation:
[1] Univ Ribeirao Preto, Unidade Biotecnol Vegetal, BR-14096900 Ribeirao Preto, SP - Brazil
[2] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Genet, BR-14049 Ribeirao Preto, SP - Brazil
Total Affiliations: 2
Document type: Journal article
Source: GENETICS AND MOLECULAR BIOLOGY; v. 36, n. 1, p. 105-110, 2013.
Web of Science Citations: 14
Abstract

Cancer has become a major public health problem worldwide and the number of deaths due to this disease is increasing almost exponentially. In the constant search for new treatments, natural products of plant origin have provided a variety of new compounds to be explored as antitumor agents. Tabernaemontana catharinensis is a medicinal plant that produces alkaloids with expressive antitumor activity, such as heyneanine, coronaridine and voacangine. The aim of present study was firstly to screen the cytotoxic activity of the indole alkaloids heyneanine, coronaridine and voacangine against HeLa (human cervix tumor), 3T3 (normal mouse embryo fibroblasts), Hep-2 (human laryngeal epithelial carcinoma) and B-16 (murine skin) cell lines by MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide); and secondly to analyze the apoptotic activity, cell membrane damage and genotoxicity of the compound that showed the best cytotoxic activity against the tumor cell lines tested. Coronaridine was the one that exhibited greater cytotoxic activity in the laryngeal carcinoma cell line Hep-2 (IC50 = 54.47 µg/mL) than the other alkaloids tested (voacangine IC50 = 159.33 µg/mL, and heyneanine IC50 = 689.45 µg/mL). Coronaridine induced apoptosis in cell lines 3T3 and Hep-2, even at high concentrations. The evaluation of genotoxicity by comet assay showed further that coronaridine caused minimal DNA damage in the Hep-2 tumor cell line, and the LDH test showed that it did not affect the plasma membrane. These results suggest that further investigation of coronaridine as an antitumor agent has merit. (AU)

FAPESP's process: 10/06245-7 - In vitro evaluation of cytotoxic and genotoxic potential OF ALKALOIDS isolated from Tabernaemontana catharinensis
Grantee:Ana Lucia Fachin Saltoratto
Support Opportunities: Regular Research Grants