International Journal of Molecular Sciences (Nov 2016)

Tapirira guianensis Aubl. Extracts Inhibit Proliferation and Migration of Oral Cancer Cells Lines

  • Renato José Silva-Oliveira,
  • Gabriela Francine Lopes,
  • Luiz Fernando Camargos,
  • Ana Maciel Ribeiro,
  • Fábio Vieira dos Santos,
  • Richele Priscila Severino,
  • Vanessa Gisele Pasqualotto Severino,
  • Ana Paula Terezan,
  • Ralph Gruppi Thomé,
  • Hélio Batista dos Santos,
  • Rui Manuel Reis,
  • Rosy Iara Maciel de Azambuja Ribeiro

DOI
https://doi.org/10.3390/ijms17111839
Journal volume & issue
Vol. 17, no. 11
p. 1839

Abstract

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Cancer of the head and neck is a group of upper aerodigestive tract neoplasms in which aggressive treatments may cause harmful side effects to the patient. In the last decade, investigations on natural compounds have been particularly successful in the field of anticancer drug research. Our aim is to evaluate the antitumor effect of Tapirira guianensis Aubl. extracts on a panel of head and neck squamous cell carcinoma (HNSCC) cell lines. Analysis of secondary metabolites classes in fractions of T. guianensis was performed using Nuclear Magnetic Resonance (NMR). Mutagenicity effect was evaluated by Ames mutagenicity assay. The cytotoxic effect, and migration and invasion inhibition were measured. Additionally, the expression level of apoptosis-related molecules (PARP, Caspases 3, and Fas) and MMP-2 was detected using Western blot. Heterogeneous cytotoxicity response was observed for all fractions, which showed migration inhibition, reduced matrix degradation, and decreased cell invasion ability. Expression levels of MMP-2 decreased in all fractions, and particularly in the hexane fraction. Furthermore, overexpression of FAS and caspase-3, and increase of cleaved PARP indicates possible apoptosis extrinsic pathway activation. Antiproliferative activity of T. guianensis extract in HNSCC cells lines suggests the possibility of developing an anticancer agent or an additive with synergic activities associated with conventional anticancer therapy.

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