Frontiers in Pharmacology (Jan 2023)

Polypodium leucotomos targets multiple aspects of oral carcinogenesis and it is a potential antitumor phytotherapy against tongue cancer growth

  • Pammela A. Lacerda,
  • Luan C. Oenning,
  • Guilherme Cuoghi Bellato,
  • Lucilene Lopes-Santos,
  • Natalícia de Jesus Antunes,
  • Bruno Augusto Linhares Almeida Mariz,
  • Gabriela Teixeira,
  • Rafael Vasconcelos,
  • Gustavo Ferreira Simões,
  • Ivani Aparecida de Souza,
  • Ivani Aparecida de Souza,
  • Clóvis Antônio Lopes Pinto,
  • Clóvis Antônio Lopes Pinto,
  • Tuula Salo,
  • Ricardo D. Coletta,
  • Ricardo D. Coletta,
  • Taize M. Augusto,
  • Taize M. Augusto,
  • Taize M. Augusto,
  • Carine Ervolino de Oliveira,
  • Carine Ervolino de Oliveira,
  • Nilva K. Cervigne,
  • Nilva K. Cervigne,
  • Nilva K. Cervigne

DOI
https://doi.org/10.3389/fphar.2022.1098374
Journal volume & issue
Vol. 13

Abstract

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Introduction: Oral cancer refers to malignant tumors, of which 90% are squamous cell carcinomas (OSCCs). These malignancies exhibit rapid progression, poor prognosis, and often mutilating therapeutical approaches. The determination of a prophylactic and/or therapeutic antitumor role of the polyphenolic extract Polypodium leucotomos(PL) would be relevant in developing new tools for prevention and treatment.Methods: We aimed to determine the antitumor effect of PL by treating OSCC cell lines with PL metabolites and evaluating its action during OSCC progression in vivo.Results: PL treatment successfully impaired cell cycling and proliferation, migration, and invasion, enhanced apoptosis, and modulated macrophage polarization associated with the tumoral immune-inflammatory response of tongue cancer cell lines (TSCC). PL treatment significantly decreased the expression of MMP1 (p < 0.01) and MMP2 (p < 0.001), and increased the expression of TIMP1 (p < 0.001) and TIMP2 (p < 0.0001) in these cells. The mesenchymal-epithelial transition phenotype was promoted in cells treated with PL, through upregulation of E-CAD (p < 0.001) and reduction of N-CAD (p < 0.05). PL restrained OSCC progression in vivo by inhibiting tumor volume growth and decreasing the number of severe dysplasia lesions and squamous cell carcinomas. Ki-67 was significantly higher expressed in tongue tissues of animals not treated with PL(p < 0.05), and a notable reduction in Bcl2 (p < 0.05) and Pcna (p < 0.05) cell proliferation-associated genes was found in dysplastic lesions and TSCCs of PL-treated mice. Finally, N-cad(Cdh2), Vim, and Twist were significantly reduced in tongue tissues treated with PL.Conclusion: PL significantly decreased OSCC carcinogenic processes in vitro and inhibited tumor progression in vivo. PL also appears to contribute to the modulation of immune-inflammatory oral tumor-associated responses. Taken together, these results suggest that PL plays an important antitumor role in processes associated with oral carcinogenesis and may be a potential phytotherapeutic target for the prevention and/or adjuvant treatment of TSCCs

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