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本文引用的文献

1
Conformationally Defined Rexinoids and Their Efficacy in the Prevention of Mammary Cancers.构象明确的视黄酸类化合物及其在预防乳腺癌方面的功效。
J Med Chem. 2015 Oct 8;58(19):7763-74. doi: 10.1021/acs.jmedchem.5b00829. Epub 2015 Sep 22.
2
Expression and Function of PPARs in Cancer Stem Cells.过氧化物酶体增殖物激活受体(PPARs)在癌症干细胞中的表达与功能
Curr Stem Cell Res Ther. 2016;11(3):226-34. doi: 10.2174/1574888x10666150728122921.
3
mTOR inhibitors counteract tamoxifen-induced activation of breast cancer stem cells.mTOR 抑制剂可拮抗他莫昔芬诱导的乳腺癌干细胞激活。
Cancer Lett. 2015 Oct 10;367(1):76-87. doi: 10.1016/j.canlet.2015.07.017. Epub 2015 Jul 21.
4
All-trans-retinoic Acid Modulates the Plasticity and Inhibits the Motility of Breast Cancer Cells: ROLE OF NOTCH1 AND TRANSFORMING GROWTH FACTOR (TGFβ).全反式维甲酸调节乳腺癌细胞的可塑性并抑制其运动性:Notch1和转化生长因子(TGFβ)的作用
J Biol Chem. 2015 Jul 17;290(29):17690-17709. doi: 10.1074/jbc.M115.638510. Epub 2015 May 27.
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Retinoic acid receptors: from molecular mechanisms to cancer therapy.维甲酸受体:从分子机制到癌症治疗。
Mol Aspects Med. 2015 Feb;41:1-115. doi: 10.1016/j.mam.2014.12.003. Epub 2014 Dec 25.
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Cooperation between BRCA1 and vitamin D is critical for histone acetylation of the p21waf1 promoter and growth inhibition of breast cancer cells and cancer stem-like cells.BRCA1与维生素D之间的合作对于p21waf1启动子的组蛋白乙酰化以及乳腺癌细胞和癌干细胞样细胞的生长抑制至关重要。
Oncotarget. 2014 Dec 15;5(23):11827-46. doi: 10.18632/oncotarget.2582.
7
Targeting cancer stem cells in solid tumors by vitamin D.维生素D靶向实体瘤中的癌症干细胞。
J Steroid Biochem Mol Biol. 2015 Apr;148:79-85. doi: 10.1016/j.jsbmb.2014.10.007. Epub 2014 Oct 16.
8
Co-delivery of all-trans-retinoic acid and doxorubicin for cancer therapy with synergistic inhibition of cancer stem cells.载阿霉素和全反式维甲酸的药物共传递用于癌症治疗并协同抑制肿瘤干细胞。
Biomaterials. 2015 Jan;37:405-14. doi: 10.1016/j.biomaterials.2014.10.018. Epub 2014 Oct 23.
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PPAR gamma gene--a review.过氧化物酶体增殖物激活受体γ基因——综述
Diabetes Metab Syndr. 2015 Jan-Mar;9(1):46-50. doi: 10.1016/j.dsx.2014.09.015. Epub 2014 Oct 13.
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Vitamin D compounds reduce mammosphere formation and decrease expression of putative stem cell markers in breast cancer.维生素D化合物可减少乳腺癌中乳腺球的形成,并降低假定干细胞标志物的表达。
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核受体在乳腺癌干细胞中的作用。

Role of nuclear receptors in breast cancer stem cells.

作者信息

Papi Alessio, Orlandi Marina

机构信息

Alessio Papi, Marina Orlandi, Department of Biological, Geological and Environmental Science (BiGea), University of Bologna, 40126 Bologna, Italy.

出版信息

World J Stem Cells. 2016 Mar 26;8(3):62-72. doi: 10.4252/wjsc.v8.i3.62.

DOI:10.4252/wjsc.v8.i3.62
PMID:27022437
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4807310/
Abstract

The recapitulation of primary tumour heterogenity and the existence of a minor sub-population of cancer cells, capable of initiating tumour growth in xenografts on serial passages, led to the hypothesis that cancer stem cells (CSCs) exist. CSCs are present in many tumours, among which is breast cancer. Breast CSCs (BCSCs) are likely to sustain the growth of the primary tumour mass, as well as to be responsible for disease relapse and metastatic spreading. Consequently, BCSCs represent the most significant target for new drugs in breast cancer therapy. Both the hypoxic condition in BCSCs biology and pro-inflammatory cytokine network has gained increasing importance in the recent past. Breast stromal cells are crucial components of the tumours milieu and are a major source of inflammatory mediators. Recently, the anti-inflammatory role of some nuclear receptors ligands has emerged in several diseases, including breast cancer. Therefore, the use of nuclear receptors ligands may be a valid strategy to inhibit BCSCs viability and consequently breast cancer growth and disease relapse.

摘要

原发肿瘤异质性的重现以及存在一小部分能够在连续传代的异种移植中启动肿瘤生长的癌细胞亚群,导致了癌症干细胞(CSCs)存在的假说。CSCs存在于许多肿瘤中,乳腺癌就是其中之一。乳腺癌症干细胞(BCSCs)可能维持原发肿瘤块的生长,并导致疾病复发和转移扩散。因此,BCSCs是乳腺癌治疗新药的最重要靶点。在最近,BCSCs生物学中的缺氧状态和促炎细胞因子网络都变得越来越重要。乳腺基质细胞是肿瘤微环境的关键组成部分,是炎症介质的主要来源。最近,一些核受体配体的抗炎作用在包括乳腺癌在内的几种疾病中显现出来。因此,使用核受体配体可能是抑制BCSCs活力从而抑制乳腺癌生长和疾病复发的有效策略。