4.4 Article

Differential effects of omega-3 PUFAS on tumor progression at early and advanced stages in TRAMP mice

期刊

PROSTATE
卷 82, 期 16, 页码 1491-1504

出版社

WILEY
DOI: 10.1002/pros.24421

关键词

dietary intervention; docosahexaenoic acid; eicosapentaenoic acid; prostate cancer; steroid receptors; transgenic adenocarcinoma of the mouse prostate

资金

  1. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior [001]
  2. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [308367/2014-6, 311635/2017]
  3. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [2019/15109-4, 2018/21891-4]

向作者/读者索取更多资源

In vitro studies have shown that omega-3 polyunsaturated fatty acids ([n-3] PUFAs) have antitumor effects, but their effects on prostate cancer remain controversial in epidemiological studies. This study found that a(n-3) PUFA-enriched diet could delay tumor progression in the early stages of prostate cancer in mice and reduce cell proliferation and hormone receptor expression.
Background In vitro studies evidenced antitumor effects of omega-3 polyunsaturated fatty acids ([n-3] PUFAs), but their effects on prostate cancer (PCa) remain controversial in epidemiological studies. Here we investigated whether an (n-3) PUFA-enriched diet affects tumor progression in transgenic adenocarcinoma of the mouse prostate (TRAMP), at early (12 weeks age) and advanced stages (20 weeks age). Methods TRAMP mice were fed with standard rodent diet (C12, C20) or (n-3) PUFA-enriched diet containing 10% fish oil (T12, T20). A group of 8 weeks age animals fed standard diet was also used for comparison (C8). The ventral prostate was processed for histopathological and immunohistochemical analyses and serum samples submitted to biochemical assays. Results At early stages, (n-3) PUFA increased the frequency of normal epithelium (3.8-fold) and decreased the frequency of high-grade intraepithelial neoplasia (3.3-fold) and in situ carcinoma (1.9-fold) in the gland, maintaining prostate pathological status similar to C8 group. At advanced stages, 50% of the animals developed a large primary tumor in both C20 and T20, and tumor weight did not differ (C20: 2.2 +/- 2.4; T20: 2.8 +/- 2.9 g). The ventral prostate of T12 and of T20 animals that did not develop primary tumors showed lower cell proliferation, tissue expressions of androgen (AR) and glucocorticoid (GR) receptors, than their respective controls. For these animals, (n-3) PUFA also avoided an increase in the number of T-lymphocytes, collagen fibers, and alpha SMA immunoreactivity, and preserved stromal gland microenvironment. (n-3) PUFA also lowered serum triglycerides and cholesterol, regulating the lipid metabolism of TRAMP mice. Conclusions (n-3) PUFAs had a protective effect at early stages of PCa, delaying tumor progression in TRAMP mice, in parallel with reductions in cell proliferation, AR, and GR and maintenance of the stromal compartment of the gland. However, (n-3) PUFAs did not prevent the development of primary tumors for the T20 group, reinforcing the need for further investigation at advanced stages of disease.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据