Laurus nobilis (laurel) aqueous leaf extract's toxicological and anti-tumor activities in HPV16-transgenic mice

B Medeiros-Fonseca1, V F Mestre, B Colaço

  • 1Center for the Research and Technology of Agro-Environmental and Biological Sciences (CITAB), University of Trás-os-Montes and Alto Douro (UTAD), Vila Real, Portugal. pamo@utad.pt.

Food & Function
|August 2, 2018
PubMed

Insights

Laurel extract did not prevent human papillomavirus 16 (HPV16)-induced skin cancer progression in mice. While showing no therapeutic effect, the extract caused mild hepatitis in wild-type mice and weight loss in transgenic mice.

Area of Science:

  • Oncology
  • Natural Products Chemistry
  • Toxicology

Background:

  • Human papillomavirus (HPV) infection is a major cause of cancer, necessitating novel therapeutic strategies.
  • Laurel (Laurus nobilis) extracts have demonstrated in vitro efficacy against HPV-transformed cells, prompting further investigation.
  • A transgenic mouse model of HPV16-induced cancer provides a platform for evaluating in vivo therapeutic potential and toxicity.

Purpose of the Study:

  • To assess the in vivo efficacy of a laurel extract in preventing or treating HPV16-induced skin cancer.
  • To evaluate the hepatic toxicity of the laurel extract in a mouse model.
  • To investigate the extract's impact on disease progression and relevant toxicological markers.

Main Methods:

  • Administration of laurel extract in drinking water to four groups of mice (wild-type and HPV16 transgenic) over three weeks.
  • Histological classification of skin lesions to assess cancer progression.
  • Toxicological evaluation including hematological and biochemical blood markers, splenic and hepatic histology, and hepatic oxidative stress analysis.

Main Results:

  • The laurel extract did not inhibit the progression of HPV16-induced cutaneous lesions in the studied mouse model.
  • Mild hepatitis was observed in wild-type mice treated with the laurel extract.
  • Transgenic mice receiving the extract experienced weight loss, but no significant changes were noted in hematological, biochemical, or hepatic oxidative stress markers.

Conclusions:

  • Laurel extract lacks efficacy in preventing HPV16-induced skin cancer progression in this in vivo model.
  • The extract exhibits potential hepatotoxicity and adverse effects such as weight loss in susceptible animal models.
  • Further research is needed to explore alternative natural compounds or refine laurel extract formulations for potential therapeutic applications.

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