African Journal of
Pharmacy and Pharmacology

  • Abbreviation: Afr. J. Pharm. Pharmacol.
  • Language: English
  • ISSN: 1996-0816
  • DOI: 10.5897/AJPP
  • Start Year: 2007
  • Published Articles: 2285

Full Length Research Paper

Cytotoxic effect of Plectranthus neochilus extracts in head and neck carcinoma cell lines

Gabriel Alvares Borges
  • Gabriel Alvares Borges
  • Faculty of Health Sciences, University of Brasília, Asa Norte, Brasília, CEP: 70910900, Brazil.
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Juliana Freitas Ferreira
  • Juliana Freitas Ferreira
  • Faculty of Health Sciences, University of Brasília, Asa Norte, Brasília, CEP: 70910900, Brazil.
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Silvia Taveira Elias
  • Silvia Taveira Elias
  • Faculty of Health Sciences, University of Brasília, Asa Norte, Brasília, CEP: 70910900, Brazil.
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Eliete Neves Silva Guerra
  • Eliete Neves Silva Guerra
  • Faculty of Health Sciences, University of Brasília, Asa Norte, Brasília, CEP: 70910900, Brazil.
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Dâmaris Silveira
  • Dâmaris Silveira
  • Faculty of Health Sciences, University of Brasília, Asa Norte, Brasília, CEP: 70910900, Brazil.
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Luiz Alberto Simeoni
  • Luiz Alberto Simeoni
  • Faculty of Health Sciences, University of Brasília, Asa Norte, Brasília, CEP: 70910900, Brazil.
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  •  Received: 12 May 2015
  •  Accepted: 11 January 2016
  •  Published: 15 March 2016

Abstract

Following a tendency of studying the potential effects of plant extracts to cancer, this study aimed to evaluate in vitro the cytotoxic activity of Plectranthus neochilus (PN) extracts and its fractions in head and neck squamous cell carcinoma (HNSCC) cell lines and assess their tumor specificity. MTT assay was conducted with two HNSCC cell lines, FaDu (hypopharynx carcinoma) and SCC-25 (tongue carcinoma), one keratinocyte (HaCat) and one fibroblast (L929) cell line. Two PN leaf crude extracts, one ethanolic (E) and one hexanic (H), and their nine fractions were tested. A dose-response curve was performed with hexane PNH fraction and a tumor specificity index (TSI) was calculated. For all cell lines studied, almost all extracts and fractions resulted in cell viability lower than 50%. Hexane and methanol PNH fractions were exceptions, causing a significantly low viability in SCC-25 (17.16 and 34.53%, respectively), but higher than 50% in FaDu, HaCat and L929. The dose-response curve with hexane PNH fraction resulted in a CC50 of 540.9 µg/mL for FaDu, 550 µg/mL for L929, 762.1 µg/mL for HaCat and 274.2 µg/mL for SCC-25. The TSI L929/FaDu was 1.01, HaCat/FaDu was 1.40, L929/SCC-25 was 2.00 and HaCat/SCC-25 was 2.77. TSIs indicate its specificity for tongue carcinoma cells, when compared to fibroblasts and keratinocytes.

Key words: Head and neck, squamous cell carcinoma, extract, cytotoxicity, cell line.