Jaboticaba Peel Extract Exerts Chemopreventive Effects in Transgenic Mouse Model of Prostate Cancer

Author:

Nogueira-Lima Ellen1ORCID,de Almeida Lamas Celina1ORCID,Baseggio Andressa Mara2ORCID,da Veiga Fernanda Cristina3ORCID,Álvares Lucia Elvira4ORCID,Júnior Mario Roberto Maróstica2ORCID,Cagnon Valeria Helena Alves1ORCID

Affiliation:

1. Department of Structural and Functional Biology, Institute of Biology, Universidade Estadual de Campinas (UNICAMP), Bertrand Russel Av, Campinas, São Paulo, 13083-865, Brazil

2. Department of Food and Nutrition, School of Food Engineering, Universidade Estadual de Campinas (UNICAMP), 80 Monteiro Lobato St, Campinas, São Paulo, 13083-852, Brazil

3. Department of Biochemistry and Tissue Biology, Biology Institute, Universidade Estadual de Campinas (UNICAMP), 255 Monteiro Lobato St, Campinas, São Paulo, 13083-970, Brazil

4. Department of Biochemistry and Tissue Biology, Biology Institute, Universidade Estadual de Campinas (UNICAMP), 255 Monteiro Lobato St, Campinas, São Paulo, 13083-970, Brazil

Abstract

Introduction: Angiogenesis, oxidative stress, and epigenetic alterations involved in prostate cancer (PCa) are associated with different risk factors, such as a high-fat diet (HFD), overweight, and obesity. Jaboticaba peel extract (PJE) has shown antiproliferative, antiangiogenic, and antioxidant activities in the prostate of senile mice. Method: This study aimed to evaluate the effect of PJE on the dorsolateral prostate microenvironment in male transgenic mice for the prostate adenocarcinoma model, considering different pathological alterations, changed or unchanged by HFD, focusing on histopathology, and molecules related to extracellular matrix (ECM), oxidative stress, angiogenesis, and Dact-1. Western blotting and immunohistochemistry were performed on Dact-1-associated tumor suppressor genes in transgenic mice. Mice were fed HFD and received patented jaboticaba peel extract (PJE) treatment. The plasma levels of systemic oxidative stress were evaluated. Results: Our results showed that PJE protected the dorsolateral prostate against proliferation and increased MMP9, TGFβ, and VEGF levels. PJE reduced oxidative stress and lipid peroxidation by modulating catalase, SOD 2, and 4HNE. PJE exhibited an epigenetic action, evidenced by increased Dact-1 gene expression in PCa. Conclusion: PJE could be a natural protector of PCa and prostate lesions associated with HFD intake.

Publisher

Bentham Science Publishers Ltd.

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