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雌激素受体β(ERβ)在乳腺癌肥胖相关炎症状态下维持线粒体网络并调节侵袭性。

Estrogen Receptor Beta (ERβ) Maintains Mitochondrial Network Regulating Invasiveness in an Obesity-Related Inflammation Condition in Breast Cancer.

作者信息

Martinez-Bernabe Toni, Sastre-Serra Jorge, Ciobu Nicolae, Oliver Jordi, Pons Daniel Gabriel, Roca Pilar

机构信息

Grupo Multidisciplinar de Oncología Traslacional, Institut Universitari d'Investigació en Ciències de la Salut (IUNICS), Universitat de les Illes Balears, 07122 Palma de Mallorca, Illes Balears, Spain.

Instituto de Investigación Sanitaria de las Islas Baleares (IdISBa), Hospital Universitario Son Espases, Edificio S, 07120 Palma de Mallorca, Illes Balears, Spain.

出版信息

Antioxidants (Basel). 2021 Aug 28;10(9):1371. doi: 10.3390/antiox10091371.

DOI:10.3390/antiox10091371
PMID:34573003
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8466315/
Abstract

Obesity, a physiological situation where different proinflammatory cytokines and hormones are secreted, is a major risk factor for breast cancer. Mitochondrial functionality exhibits a relevant role in the tumorigenic potential of a cancer cell. In the present study, it has been examined the influence of an obesity-related inflammation ELIT treatment (17β-estradiol, leptin, IL-6, and TNFα), which aims to stimulate the hormonal conditions of a postmenopausal obese woman on the mitochondrial functionality and invasiveness of MCF7 and T47D breast cancer cell lines, which display a different ratio of both estrogen receptor isoforms, ERα and ERβ. The results showed a decrease in mitochondrial functionality, with an increase in oxidative stress and invasiveness and motility, in the MCF7 cell line (high ERα/ERβ ratio) compared to a maintained status in the T47D cell line (low ERα/ERβ ratio) after ELIT treatment. In addition, breast cancer biopsies were analyzed, showing that breast tumors of obese patients present a high positive correlation between IL-6 receptor and ERβ and have an increased expression of cytokines, antioxidant enzymes, and mitochondrial biogenesis and dynamics genes. Altogether, giving special importance to ERβ in the pathology of obese patients with breast cancer is necessary, approaching to personalized medicine.

摘要

肥胖是一种会分泌多种促炎细胞因子和激素的生理状态,是乳腺癌的主要危险因素。线粒体功能在癌细胞的致瘤潜能中发挥着重要作用。在本研究中,研究了一种与肥胖相关的炎症ELIT治疗(17β-雌二醇、瘦素、白细胞介素-6和肿瘤坏死因子α)的影响,该治疗旨在模拟绝经后肥胖女性的激素状况,对MCF7和T47D乳腺癌细胞系的线粒体功能和侵袭性进行研究,这两种细胞系中雌激素受体亚型ERα和ERβ的比例不同。结果显示,与ELIT治疗后T47D细胞系(ERα/ERβ比例低)的线粒体功能维持稳定相比,MCF7细胞系(ERα/ERβ比例高)的线粒体功能下降,氧化应激、侵袭性和运动性增加。此外,对乳腺癌活检组织进行分析,结果表明肥胖患者的乳腺肿瘤中白细胞介素-6受体与ERβ之间呈高度正相关,且细胞因子、抗氧化酶以及线粒体生物发生和动力学相关基因的表达增加。总之,在乳腺癌肥胖患者的病理研究中重视ERβ很有必要,这有助于实现个性化医疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eea/8466315/20f1a42070e3/antioxidants-10-01371-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eea/8466315/20f1a42070e3/antioxidants-10-01371-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eea/8466315/1cc48bc313ca/antioxidants-10-01371-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eea/8466315/20f1a42070e3/antioxidants-10-01371-g008.jpg

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本文引用的文献

1
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2
Therapeutic potential of targeting mitochondrial dynamics in cancer.靶向线粒体动力学在癌症治疗中的潜力
Biochem Pharmacol. 2020 Dec;182:114282. doi: 10.1016/j.bcp.2020.114282. Epub 2020 Oct 12.
3
Micronutrients Selenomethionine and Selenocysteine Modulate the Redox Status of MCF-7 Breast Cancer Cells.硒代蛋氨酸和硒代半胱氨酸等微量营养素调节 MCF-7 乳腺癌细胞的氧化还原状态。
Estrogen receptors in mitochondrial metabolism: age-related changes and implications for pregnancy complications.
线粒体代谢中的雌激素受体:年龄相关变化及其对妊娠并发症的影响。
Aging Adv. 2024 Dec;1(2):154-171. doi: 10.4103/agingadv.agingadv-d-24-00012. Epub 2024 Dec 20.
4
Obesity-Related Inflammation Reduces Treatment Sensitivity and Promotes Aggressiveness in Luminal Breast Cancer Modulating Oxidative Stress and Mitochondria.肥胖相关炎症通过调节氧化应激和线粒体降低腔面型乳腺癌的治疗敏感性并促进其侵袭性。
Biomedicines. 2024 Dec 11;12(12):2813. doi: 10.3390/biomedicines12122813.
5
Tumorspheres as In Vitro Model for Identifying Predictive Chemoresistance and Tumor Aggressiveness Biomarkers in Breast and Colorectal Cancer.肿瘤球作为鉴定乳腺癌和结直肠癌预测性化疗耐药性及肿瘤侵袭性生物标志物的体外模型
Biology (Basel). 2024 Sep 15;13(9):724. doi: 10.3390/biology13090724.
6
A new therapeutic strategy for luminal A-breast cancer treatment: vulpinic acid as an anti-neoplastic agent induces ferroptosis and apoptosis mechanisms.治疗 luminal A 型乳腺癌的新策略:熊果酸作为一种抗肿瘤药物,诱导铁死亡和细胞凋亡机制。
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7
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8
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5
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6
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Mol Cancer Res. 2019 Nov;17(11):2184-2195. doi: 10.1158/1541-7786.MCR-18-1194. Epub 2019 Aug 19.
7
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8
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Am J Physiol Cell Physiol. 2019 Aug 1;317(2):C398-C404. doi: 10.1152/ajpcell.00112.2019. Epub 2019 Jun 12.
9
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Cytokine. 2019 Aug;120:155-164. doi: 10.1016/j.cyto.2019.04.016. Epub 2019 May 11.
10
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Int J Food Sci Nutr. 2019 Dec;70(8):941-949. doi: 10.1080/09637486.2019.1597025. Epub 2019 Apr 4.