没食子酸对双酚A内分泌干扰损伤的保护作用及可能机制

Bekir Nihat Doğrul, Ibrahim Kiliccalan, Ekrem Samet Aşçı
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引用次数: 4

摘要

癌症是由于DNA损伤导致的不受控制和/或异常的细胞生长和增殖。当正常细胞受到DNA损伤时,它们试图通过各种机制来防止这种损伤。但在癌症中,细胞的修复机制被破坏了。细胞过度和不正常地生长,这威胁到生物体的生命。导致致癌的因素有很多。其中一个因素是内分泌干扰物。内分泌干扰物可以破坏人体机制,模仿体内的某些激素。双酚a (BPA)是一种内分泌干扰物质,存在于许多产品中,如塑料瓶,主要包括包装食品。暴露于双酚a会引起类似雌激素的特征,这可能通过细胞中的雌激素代谢导致致癌。酚类化合物广泛存在于植物中,对人体有益,通常被认为是人体的健康营养素。我们认为,酚类化合物可能对雌激素代谢对BPA有一定的积极作用。证明:证明;将未食子酸(酚类化合物的原型)、双酚a和纯雌激素受体阻滞剂(氟维司群)应用于DU-145(恶性前列腺癌细胞)和HGF-1(人牙龈成纤维细胞)细胞系。氟维司汀检测雌激素受体相关疗效。我们使用MTT测试来测量我们使用的化学物质的细胞毒性。采用Real-Time PCR法研究双酚a和没食子酸对雌激素代谢的影响。在我们的研究中,MTT试验表明没食子酸降低了细胞中BPA的细胞毒性。氟维司汀与没食子酸或双酚a联合使用,也改变了MTT试验中细胞存活率的百分比,但这些变化微不足道。因此,可以认为BPA与没食子酸的相关作用不仅仅是通过雌激素受体α和雌激素受体β产生的。通过RT-PCR研究,我们确定没食子酸和BPA对细胞内雌激素代谢酶有影响。氟维司汀改变了没食子酸和双酚a的作用。这表明这些物质可能通过雌激素受体发挥作用。本研究最有希望的结果之一是:没食子酸增加了GST酶的mRNA表达,增加了解毒作用和QR酶的表达,减少了DNA加合物。这表明没食子酸对肿瘤的致癌特性也有保护作用,对双酚a等化学物质的内分泌干扰也有保护作用。没食子酸还增加了良性细胞中PARP酶mRNA的表达,但在恶性细胞中没有特异性的增加,这是DNA修复机制的重要一步。我们计划进行新的RT-PCR和Western Blot研究,以更准确地确定雌激素受体和雌激素代谢相关酶在多癌、乳腺癌和前列腺癌细胞系中酚类化合物对内分泌干扰物的预防作用机制中的可能作用。我们相信这对于理解内分泌干扰物和癌症的潜在机制将是非常有用的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The protective effect of gallic acid against endocrine disrupting damages of Bisphenol A and possible mechanism
Cancer is uncontrolled and/or abnormal cell growth and proliferation as a result of DNA damage. When the normal cells are exposed to DNA damage they try to prevent this damage through various mechanisms. But in cancer, repair mechanisms of the cell are disrupted. Cells grow excessively and abnormally and this threatens the life of organism. There are many factors that lead to carcinogenesis. One of these factors is endocrine disruptors. Endocrine disruptors can damage the body mechanisms to mimic certain hormones in the body. Bisphenol-A (BPA), which is one of the endocrine disrupting substances, is found in many products such as plastic bottles, including primarily packaged foods. Exposure to BPA causes estrogen-mimetic feature which may lead to carcinogenesis through estrogen metabolism in cells. Phenolic compounds are widely present in plants which had beneficial effects on the body, and generally considered as health nutrients for human. We think, the phenolic compounds could have some positive effects on estrogen metabolism against BPA. To demonstrate that; gallic acid –which is a prototype of phenolic compounds-, Bisphenol A and pure estrogen receptor blocker (fulvestrant) were applied to DU-145 (malign prostatic cancer cell) and HGF-1 (human gingival fibroblast cell) cell lines. Fulvestrant was used to detect estrogen receptors related efficacy. We used MTT test to measure the cytotoxicity of chemical substances that we used. Effects of BPA and gallic acid on estrogen metabolism were investigated by Real-Time PCR method. In our study, MTT test showed that the gallic acid decreased the cytotoxicity of BPA in cells. Using fulvestrant in combination with gallic acid or BPA, also changed the percent of cell viability in MTT test, but these changes were negligible amount. Therefore, it could be considered that BPA and gallic acid related effects are not only via estrogen receptor alpha and estrogen receptor beta. As a result of studies conducted by RT-PCR, we determined that gallic acid and BPA had effects on enzymes of intracellular estrogen metabolism. Fulvestrant caused changes on the effects of gallic acid and BPA. This shows us that the these substances may show their effects via estrogen receptors. One of the most promising results of this study was: gallic acid increased the expression of mRNA expression of GST enzyme which increases detoxification and QR enzyme that decreases the DNA adducts. This showed us gallic acid can also do protective effects to carcinogenic properties as well as endocrine disrupting effects of chemicals like Bisphenol A. Gallic acid also increased the expression of mRNA expression of PARP enzyme in benign cells, but not in malign cells specifically, which is an important step in DNA repair mechanism. We planned a new RT-PCR and Western Blot study in order to determine the possible role of estrogen receptors and estrogen metabolism related enzymes in the mechanism of the preventive effect of phenolic compounds against endocrine disrupters more precisely, in over cancer, mammary cancer and prostate cancer cell lines. And we believed that this would be very informative for the understanding the underlying mechanism of endocrine disrupters and cancer.
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