Laurencia johnstonii extract reverses early lesions in the K14E7HPV16 murine cervical carcinogenesis model

Author:

Arvizu‐Hernandez Erandi12,Hernandez‐Guerrero Claudia Judith3,Alvarez‐Rios Elizabeth2,Gariglio Patricio2ORCID,Cornejo‐Garrido Jorge1,Ocadiz‐Delgado Rodolfo2ORCID

Affiliation:

1. Laboratory of Cellular Biology and Natural Products I, Escuela Nacional de Medicina y Homeopatía Instituto Politécnico Nacional La Paz Mexico

2. Department of Genetics and Molecular Biology Centro de Investigación y de Estudios Avanzados IPN Ciudad de Mexico Mexico

3. Department of Technologies Development, Centro Interdisciplinario de Ciencias Marinas Instituto Politécnico Nacional La Paz B.C.S. Mexico

Abstract

AbstractPersistent infection with high‐risk human papillomavirus (HR‐HPV) is a well‐established risk factor to the development of cervical intraepithelial neoplasia (CIN), a condition that can progress to cervical cancer (CC) a major health problem worldwide. Recently, there has been growing interest in exploring alternative therapies utilizing natural products, among which is the algae species Laurencia johnstonii Setchell & Gardner, 1924 (L. johnstonii), proposed for the management of precancerous lesions. The aim of this work was to determine the effect of an organic extract from L. johnstonii (ELj) in early cervical lesions (CIN 1). These CIN 1 lesions were generated in a murine model expressing the HR‐HPV16 E7 oncoprotein (K14E7HPV transgenic mice) with a single exogenous hormonal stimulus using 17β‐estradiol. The histopathological studies, the determination of cell proliferation and of the apoptotic levels in cervical tissue, showed that, seven doses of ELj (30 mg/kg weight per day diluted in a DMSO‐saline solution [1:7]) lead to recovery the architecture of cervical epithelium. Accordingly, in the transgenic mice it was observed a statistically significant decrease of the PCNA expression levels, a marker of cell proliferation, and a statistically significant increase in the apoptosis levels using Caspase 3 as a marker. In addition, we determined the expression levels of the tumor suppressor miR‐218 and the oncomiRNA miR‐21. Interestingly, our results may suggest that ELj treatment tended to restore the normal expression of both miRNAs as compared with controls being more evident in the non‐transgenic induced mice. Differences of p < 0.05 were considered statistically significant through the whole study. Based on these results, we propose that the use of ELj could be an alternative for the treatment of cervical early lesions.

Publisher

Wiley

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