Laboratory of Biochemistry and Immunology, College of Veterinary Medicine, Chungbuk National University, Cheongju, Chungbuk, Republic of Korea.
Laboratory of Biochemistry and Immunology, College of Veterinary Medicine, Chungbuk National University, Cheongju, Chungbuk, Republic of Korea.
Mol Cell Endocrinol. 2017 Dec 5;457:103-113. doi: 10.1016/j.mce.2016.12.026. Epub 2016 Dec 29.
Endocrine disrupting chemicals (EDCs) are natural or synthetic compounds that interfere with normal functions of natural hormones in the body, leading to a disruption of the endocrine system. Specifically, EDCs have the potential to cause formation of several hormone-dependent cancers, including breast, ovarian, and prostate cancers. Epithelial mesenchymal transition (EMT) process by which epithelial cells lose their cell polarity and cell-cell adhesion and acquire mesenchymal phenotype is closely associated with malignant transformation and the initiation of cancer metastasis. As a key epithelial marker responsible for adherens junction, E-cadherin enables the cells to maintain epithelial phenotypes. EMT event is induced by E-cadherin loss which can be carried out by many transcription factors (TFs), including Snail, Slug, ZEB1, ZEB2, Kruppel-like factor 8 (KLF8), and Twist. N-cadherin, fibronectin, and vimentin are mesenchymal markers needed for cellular migration. The EMT process is regulated by several signaling pathways mediated by transforming growth factor β (TGF-β), Wnt-β-catenin, Notch, Hedgehog, and receptor tyrosine kinases. In the present article, we reviewed the current understanding of cancer progression effects of synthetic chemical EDCs such as bisphenol A (BPA), phthalates, tetrachlorodibenzo-p-dioxin (TCDD), and triclosan by focusing their roles in the EMT process. Collectively, the majority of previous studies revealed that BPA, phthalates, TCDD, and triclosan have the potential to induce cancer metastasis through regulating EMT markers and migration via several signaling pathways associated with the EMT program. Therefore, it is considered that the exposure to these EDCs can increase the risk aggravating the disease for the patients suffering cancer and that more regulations about the use of these EDCs are needed.
内分泌干扰化学物质(EDCs)是天然或合成的化合物,它们干扰体内天然激素的正常功能,导致内分泌系统紊乱。具体来说,EDCs 有可能导致几种激素依赖性癌症的形成,包括乳腺癌、卵巢癌和前列腺癌。上皮间质转化(EMT)过程中,上皮细胞失去细胞极性和细胞间黏附性,并获得间充质表型,与恶性转化和癌症转移的启动密切相关。E-钙黏蛋白作为负责黏着连接的关键上皮标志物,使细胞能够维持上皮表型。EMT 事件是由许多转录因子(TFs)诱导的,包括 Snail、Slug、ZEB1、ZEB2、Krüppel 样因子 8(KLF8)和 Twist,E-钙黏蛋白的丢失会导致 EMT 的发生。N-钙黏蛋白、纤连蛋白和波形蛋白是细胞迁移所需的间充质标志物。EMT 过程受转化生长因子β(TGF-β)、Wnt-β-catenin、Notch、Hedgehog 和受体酪氨酸激酶介导的几种信号通路调节。在本文中,我们综述了合成化学 EDC 如双酚 A(BPA)、邻苯二甲酸酯、四氯二苯并对二恶英(TCDD)和三氯生对癌症进展的影响,重点关注它们在 EMT 过程中的作用。总的来说,大多数先前的研究表明,BPA、邻苯二甲酸酯、TCDD 和三氯生通过调节 EMT 标志物和与 EMT 程序相关的几种信号通路的迁移,有可能诱导癌症转移。因此,认为接触这些 EDCs 会增加癌症患者疾病恶化的风险,需要对这些 EDCs 的使用进行更多的监管。