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纳米银对丁基羟基苯甲酸酯或邻苯二甲酸二丁酯诱导的雌激素依赖性MCF-7/BUS人乳腺癌细胞增殖的抑制作用。

Inhibitory effect of silver nanoparticles on proliferation of estrogen-dependent MCF-7/BUS human breast cancer cells induced by butyl paraben or di-n-butyl phthalate.

作者信息

Roszak Joanna, Smok-Pieniążek Anna, Domeradzka-Gajda Katarzyna, Grobelny Jarosław, Tomaszewska Emilia, Ranoszek-Soliwoda Katarzyna, Celichowski Grzegorz, Stępnik Maciej

机构信息

Department of Toxicology and Carcinogenesis, Nofer Institute of Occupational Medicine, 8 St Teresy St., 91-348 Łódź, Poland.

Department of Toxicology and Carcinogenesis, Nofer Institute of Occupational Medicine, 8 St Teresy St., 91-348 Łódź, Poland.

出版信息

Toxicol Appl Pharmacol. 2017 Dec 15;337:12-21. doi: 10.1016/j.taap.2017.10.014. Epub 2017 Oct 23.

Abstract

In this study the effect of silver nanoparticles (AgNPs) on proliferation of estrogen receptor (ER)-positive human breast cancer MCF-7/BUS cells was assessed by means of in vitro assay. The cells were exposed in the absence of estrogens to AgNPs alone or in combination with aluminum chloride (AlCl), butyl paraben (BPB) and di-n-butyl phthalate (DBPh). The results revealed that AgNPs at the non-cytotoxic concentrations (up to 2μg/mL) and AlCl (up to 500μM) did not induce proliferation of MCF-7/BUS cells whereas BPB and DBPh showed strong estrogenic activity with the highest effect at 16μM and 35μM, respectively. AgNPs inhibited the proliferation of the cells induced by DBPh, BPB or even with 17β-estradiol (E2) during 6-day incubation in the absence of estrogens. ICI 182,780 (10nM), a known estrogen receptor (ER) antagonist, induced strong inhibitory effect. AgNPs also decreased transcription of the estrogen-responsive pS2 and progesterone receptor (PGR) genes but modulated expression neither of ERα nor ERβ in MCF-7/BUS cells exposed to BPB, DBPh or E2 for 6h. Our results indicate that AgNPs may inhibit growth of breast cancer cells stimulated by E2 or estrogenic chemicals, i.e. BPB and DBPh.

摘要

在本研究中,通过体外试验评估了银纳米颗粒(AgNPs)对雌激素受体(ER)阳性人乳腺癌MCF-7/BUS细胞增殖的影响。在无雌激素的情况下,将细胞单独暴露于AgNPs或与氯化铝(AlCl)、对羟基苯甲酸丁酯(BPB)和邻苯二甲酸二正丁酯(DBPh)联合暴露。结果显示,非细胞毒性浓度(高达2μg/mL)的AgNPs和AlCl(高达500μM)未诱导MCF-7/BUS细胞增殖,而BPB和DBPh表现出较强的雌激素活性,分别在16μM和35μM时效果最佳。在无雌激素的6天孵育期间,AgNPs抑制了由DBPh、BPB甚至17β-雌二醇(E2)诱导的细胞增殖。已知的雌激素受体(ER)拮抗剂ICI 182,780(10nM)诱导了强烈的抑制作用。在暴露于BPB、DBPh或E2 6小时的MCF-7/BUS细胞中,AgNPs还降低了雌激素反应性pS2和孕激素受体(PGR)基因的转录,但未调节ERα和ERβ的表达。我们的结果表明,AgNPs可能抑制由E2或雌激素化学物质(即BPB和DBPh)刺激的乳腺癌细胞生长。

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