Ramos Carina, Ladeira Carina, Zeferino Sofia, Dias Ana, Faria Isabel, Cristovam Elisabete, Gomes Manuel, Ribeiro Edna
Escola Superior de Tecnologia da Saúde de Lisboa - Instituto Politécnico de Lisboa (ESTeSL-IPL), Av. D. João II, lote 4.69.01, 1990-096, Parque das Nações, Lisboa, Portugal.
Escola Superior de Tecnologia da Saúde de Lisboa - Instituto Politécnico de Lisboa (ESTeSL-IPL), Av. D. João II, lote 4.69.01, 1990-096, Parque das Nações, Lisboa, Portugal; Health and Technology Research Center, Escola Superior de Tecnologia da Saúde de Lisboa - Instituto Politécnico de Lisboa (ESTeSL-IPL), Av. D. João II, lote 4.69.01, 1990-096, Parque das Nações, Lisboa, Portugal; Centro de Investigação em Saúde Pública, Escola Nacional de Saúde Pública - Universidade Nova de Lisboa, 1900, Lisboa, Portugal.
Mutat Res Genet Toxicol Environ Mutagen. 2019 Feb;838:28-36. doi: 10.1016/j.mrgentox.2018.11.009. Epub 2018 Nov 27.
Bisphenol A (BPA) is one of the most widely utilized endocrine disruptors to which humans are exposed, particularity through ingestion. BPA is an aneugenic compound with a putative association to tumorigenesis. Although extensively studied in estrogen responsive cells, information regarding its effects on cells from the upper gastrointestinal tract exposed to free/active forms of BPA is still scarce. Similarly, BPA interactions with other drugs have been neglected, although it has been suggested to have a potential role in doxorubicin (DOX) chemoresistance. This study is intended to assess potential cytotoxic and genotoxic effects of BPA, as well as its interactions with DOX, in Human epithelial type 2 cells (Hep-2) originated from a human laryngeal carcinoma and in a DNA damage responsive cell line, the human lung fibroblasts (MRC-5). Cell viability was analyzed through the resazurin assay. The G protein-coupled estrogen receptor 1 (GPER) expression was visualized by immunodetection. Genotoxicity, namely DNA damage and oxidative DNA damage, were assessed by comet assay and micronuclei induction, and mitotic disruption was evaluated cytologically by fluorescent microscopy with DAPI staining. Cytotoxicity analysis showed that exposure to BPA per se does not affect cellular viability. Nevertheless, the genotoxic analysis showed that BPA induced an increase of DNA damage in the Hep-2 cell line and in oxidative damage in the MRC-5 cell line. An increase of micronuclei was also observed in both cell lines following BPA exposure. BPA and DOX co-exposures suggested that BPA acts as an antagonist of DOX effects in both cell lines. The interaction with DOX appears to be cell type dependent, exhibiting a non-monotonic response curve in MRC-5 cells, a GPER expressing cell line. Our study emphasizes the need for a deeper knowledge of BPA interactions, particularly with chemotherapeutic agents, in the context of risk assessment and public health.
双酚A(BPA)是人类接触最为广泛的内分泌干扰物之一,尤其是通过摄入接触。BPA是一种非整倍体化合物,与肿瘤发生可能存在关联。尽管在雌激素反应性细胞中已进行了广泛研究,但关于其对暴露于游离/活性形式BPA的上消化道细胞的影响的信息仍然匮乏。同样,BPA与其他药物的相互作用也被忽视了,尽管有人提出它在阿霉素(DOX)化疗耐药中可能发挥潜在作用。本研究旨在评估BPA对源自人喉癌的人上皮2型细胞(Hep-2)和DNA损伤反应细胞系人肺成纤维细胞(MRC-5)的潜在细胞毒性和遗传毒性作用,以及它与DOX的相互作用。通过刃天青测定法分析细胞活力。通过免疫检测观察G蛋白偶联雌激素受体1(GPER)的表达。通过彗星试验和微核诱导评估遗传毒性,即DNA损伤和氧化性DNA损伤,并通过DAPI染色的荧光显微镜进行细胞学评估有丝分裂破坏。细胞毒性分析表明,单独暴露于BPA不会影响细胞活力。然而,遗传毒性分析表明,BPA在Hep-2细胞系中诱导DNA损伤增加,在MRC-5细胞系中诱导氧化性损伤增加。BPA暴露后,两个细胞系中也观察到微核增加。BPA和DOX共同暴露表明,BPA在两个细胞系中均作为DOX效应的拮抗剂。与DOX的相互作用似乎依赖于细胞类型,在表达GPER的细胞系MRC-5细胞中呈现非单调反应曲线。我们的研究强调,在风险评估和公共卫生背景下,需要更深入了解BPA的相互作用,特别是与化疗药物的相互作用。