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p53在人乳腺上皮癌细胞中诱导金属硫蛋白的潜在作用。

Potential role of p53 on metallothionein induction in human epithelial breast cancer cells.

作者信息

Fan L Z, Cherian M G

机构信息

Department of Pathology, University of Western Ontario, London, Ontario, N6A 5C1, Canada.

出版信息

Br J Cancer. 2002 Oct 21;87(9):1019-26. doi: 10.1038/sj.bjc.6600549.

Abstract

The expression and induction of metallothionein has been associated with protection against oxidative stress and apoptosis. This study examines the effect of tumour suppressor protein p53 on metallothionein expression following CdCl2 treatment in eight human epithelial breast cancer cell lines differing in p53 and oestrogen-receptor status. Cells were treated with 10 microM CdCl2 for 24 h and metallothionein protein levels were measured by cadmium binding assay. MCF7 cells which are p53-positive (p53+) and oestrogen-receptor-positive showed a large induction in metallothionein synthesis by 10.79+/-1.36-fold. Other breast cancer cell lines which are p53-negative (p53-) and oestrogen-receptor-negative or weakly oestrogen-receptor-positive showed a small induction ranging from 1.40+/-0.10 to 3.65+/-0.30-fold. RT-PCR analysis showed an induction of metallothionein mRNA in MCF7 cells by about 1.61+/-0.08-fold, while in HCC1806 cells (p53-, oestrogen-receptor-negative) by 1.11+/-0.13-fold, and in MDA-MB-231 (p53-, oestrogen-receptor-negative) by 1.25+/-0.06-fold. Metallothionein localisation was determined by immunohistochemical staining. Prior to metal treatment, metallothionein was localised mainly in the cytoplasm of MCF7 and MDA-MB-231 cells. After treatment with 10 microM CdCl2 for 24 h, MCF7 cells showed intense nuclear and cytoplasmic staining for metallothionein, while MDA-MB-231 cells showed staining in the cytoplasm with weak nuclear staining. Apoptosis induced by 10-40 microM CdCl2 at time points between 4 and 48 h was examined with TUNEL assay. In MCF7 cells, apoptosis increased with higher concentrations of CdCl2, it peaked at 6-8 h and appeared again at 48 h for all concentrations of CdCl2 tested. In MDA-MB-231 cells, apoptosis remained at low levels for 10-40 microM CdCl2 at all time points. Studies on cadmium uptake showed similar uptake and accumulation of cadmium at 8 and 24 h in all the cell lines. The data demonstrate that treatment of epithelial breast cancer cells with 10 microM CdCl2 for 24 h caused a greater induction of metallothionein protein and mRNA expression in p53+ and oestrogen-receptor-positive cells as compared to p53- and oestrogen-receptor-negative or weakly oestrogen-receptor-positive cells. This effect may be associated with the occurrence of apoptosis and suggests a role for p53 and oestrogen-receptor on the expression and induction of metallothionein in epithelial cells.

摘要

金属硫蛋白的表达与诱导同抵御氧化应激和细胞凋亡相关。本研究检测了肿瘤抑制蛋白p53对八个人类乳腺上皮癌细胞系在氯化镉处理后金属硫蛋白表达的影响,这些细胞系的p53和雌激素受体状态各不相同。细胞用10微摩尔/升氯化镉处理24小时,通过镉结合试验测定金属硫蛋白的蛋白水平。p53阳性(p53+)且雌激素受体阳性的MCF7细胞显示金属硫蛋白合成大幅诱导,增加了10.79±1.36倍。其他p53阴性(p53-)且雌激素受体阴性或雌激素受体弱阳性的乳腺癌细胞系显示诱导程度较小,在1.40±0.10至3.65±0.30倍之间。逆转录聚合酶链反应(RT-PCR)分析显示,MCF7细胞中金属硫蛋白信使核糖核酸(mRNA)诱导约1.61±0.08倍,而在HCC1806细胞(p53-,雌激素受体阴性)中为1.11±0.13倍,在MDA-MB-231细胞(p53-,雌激素受体阴性)中为1.25±0.06倍。通过免疫组织化学染色确定金属硫蛋白的定位。在金属处理前,金属硫蛋白主要定位于MCF7和MDA-MB-231细胞的细胞质中。用10微摩尔/升氯化镉处理24小时后,MCF7细胞显示金属硫蛋白在细胞核和细胞质中有强烈染色,而MDA-MB-231细胞显示细胞质中有染色,细胞核染色较弱。在4至48小时的时间点,用末端脱氧核苷酸转移酶介导的缺口末端标记法(TUNEL)检测10至40微摩尔/升氯化镉诱导细胞凋亡的情况。在MCF7细胞中,凋亡随氯化镉浓度升高而增加,在6至8小时达到峰值,并且在所有测试的氯化镉浓度下于48小时再次出现。在MDA-MB-231细胞中,对于10至40微摩尔/升氯化镉,在所有时间点凋亡均维持在低水平。镉摄取研究表明,在所有细胞系中,8小时和24小时时镉的摄取和积累情况相似。数据表明,与p53阴性且雌激素受体阴性或雌激素受体弱阳性的细胞相比,用10微摩尔/升氯化镉处理上皮乳腺癌细胞24小时会导致p53阳性且雌激素受体阳性的细胞中金属硫蛋白的蛋白和mRNA表达有更大诱导。这种效应可能与细胞凋亡的发生有关,并提示p53和雌激素受体在上皮细胞中金属硫蛋白的表达和诱导方面发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa5d/2364318/c58920b40e13/87-6600549f1.jpg

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