4.7 Article

Impacts of endocrine-disrupting chemicals on prostate function and cancer

期刊

ENVIRONMENTAL RESEARCH
卷 204, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.envres.2021.112085

关键词

Genistein; Bisphenol; Steroid; Phthalate; Phytoestrogen

资金

  1. Natural Sciences and Engineering Research Council of Canada

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EDCs can modulate the functions of sex-steroid receptors, indirectly impact androgen and estrogen pathways, and have multiple cellular targets beyond sex-steroid receptors, leading to various potential effects. This article reviews the association between prostate cancer and the endocrine-disrupting functions of four prominent EDC families, suggesting common guidelines for studying EDCs in the context of endocrine diseases.
Because of their historical mode of action, endocrine-disrupting chemicals (EDCs) are associated with sex-steroid receptors, namely the two estrogen receptors (ER alpha and ER beta) and the androgen receptor (AR). Broadly, EDCs can modulate sex-steroid receptor functions. They can also indirectly impact the androgen and estrogen pathways by influencing steroidogenesis, expression of AR or ERs, and their respective activity as transcription factors. Additionally, many of these chemicals have multiple cellular targets other than sex-steroid receptors, which results in a myriad of potential effects in humans. The current article reviews the association between prostate cancer and the endocrine-disrupting functions of four prominent EDC families: bisphenols, phthalates, phytoestrogens, and mycoestrogens. Results from both in vitro and in vivo models are included and discussed to better assess the molecular mechanisms by which EDCs can modify prostate biology. To overcome the heterogeneity of results published, we established common guidelines to properly study EDCs in the context of endocrine diseases. Firstly, the expression of sex-steroid receptors in the models used must be determined before testing. Then, in parallel to EDCs, pharmacological compounds acting as positive (agonists) and negative controls (antagonists) have to be employed. Finally, EDCs need to be used in a precise range of concentrations to modulate sex-steroid receptors and avoid off-target effects. By adequately integrating molecular endocrinology aspects in EDC studies and identifying their underlying molecular mechanisms, we will truly understand their impact on prostate cancer and distinguish those that favor the progression of the disease from those that slow down tumor development.

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