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雌激素对微小RNA的抑制作用与其前体末端环序列中的高鸟嘌呤含量相关。

Estrogen Repression of MicroRNAs Is Associated with High Guanine Content in the Terminal Loop Sequences of Their Precursors.

作者信息

Cohen Amit, Burgos-Aceves Mario Alberto, Kahan Tamar, Smith Yoav

机构信息

Genomic Data Analysis Unit, The Hebrew University of Jerusalem-Hadassah Medical School, P.O. Box 12272, Jerusalem 91120, Israel.

Laboratorio de Endocrinología, Centro de Investigaciones Biológicas del Noroeste, Instituto Politécnico Nacional 195, Playa Palo de Santa Rita Sur, La Paz 23096, B.C.S., Mexico.

出版信息

Biomedicines. 2017 Aug 14;5(3):47. doi: 10.3390/biomedicines5030047.

DOI:10.3390/biomedicines5030047
PMID:28805722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5618305/
Abstract

Widespread microRNA (miRNA) repression is a phenomenon observed in mammals after exposure to cigarette smoke and in many types of cancer. A comprehensive reduction in miRNA expression after treatment with the hormone estrogen has also previously been described. Here, we reveal a conserved association of miRNA downregulation after estrogen exposure in zebrafish, mouse, and human breast cancer cell line, with a high guanine content in the terminal loop sequences of their precursors, and offer a possible link between estrogen-related miRNA-adducts formation and carcinogenesis. We also show common gene expression patterns shared by breast cancer tumors and estrogen-treated zebrafish, suggesting that this organism can be used as a powerful model system for the study of human breast cancer.

摘要

广泛的微小RNA(miRNA)抑制是在哺乳动物接触香烟烟雾后以及在许多类型癌症中观察到的一种现象。此前也有关于用雌激素处理后miRNA表达全面降低的描述。在这里,我们揭示了斑马鱼、小鼠和人乳腺癌细胞系在雌激素暴露后miRNA下调的保守关联,其前体的末端环序列中鸟嘌呤含量较高,并提出了雌激素相关miRNA加合物形成与致癌作用之间可能的联系。我们还展示了乳腺癌肿瘤和雌激素处理的斑马鱼共有的常见基因表达模式,表明这种生物体可作为研究人类乳腺癌的强大模型系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab70/5618305/e6c6bd9eca28/biomedicines-05-00047-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab70/5618305/c5144bda2433/biomedicines-05-00047-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab70/5618305/eea7bdd2a09c/biomedicines-05-00047-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab70/5618305/e6c6bd9eca28/biomedicines-05-00047-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab70/5618305/c5144bda2433/biomedicines-05-00047-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab70/5618305/eea7bdd2a09c/biomedicines-05-00047-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab70/5618305/e6c6bd9eca28/biomedicines-05-00047-g003.jpg

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本文引用的文献

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Genetic variation and RNA structure regulate microRNA biogenesis.遗传变异和 RNA 结构调节 microRNA 的生物发生。
Nat Commun. 2017 May 3;8:15114. doi: 10.1038/ncomms15114.
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ERK Activation Globally Downregulates miRNAs through Phosphorylating Exportin-5.细胞外信号调节激酶(ERK)激活通过磷酸化核输出蛋白5在整体上下调微小RNA(miRNA)。
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非特异性蛋白质修饰可能是生物活性植物化学物质的潜在新机制。
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A potential role for estrogen in cigarette smoke-induced microRNA alterations and lung cancer.雌激素在香烟烟雾诱导的 microRNA 改变和肺癌中的潜在作用。
Transl Lung Cancer Res. 2016 Jun;5(3):322-30. doi: 10.21037/tlcr.2016.06.08.
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Depurinating estrogen-DNA adducts, generators of cancer initiation: their minimization leads to cancer prevention.脱嘌呤雌激素-DNA加合物,癌症起始的引发剂:使其最小化可预防癌症。
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Estrogen repression of microRNA as a potential cause of cancer.雌激素对微小RNA的抑制作用可能是癌症的一个潜在病因。
Biomed Pharmacother. 2016 Mar;78:234-238. doi: 10.1016/j.biopha.2016.01.023. Epub 2016 Feb 2.
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MicroRNA biogenesis pathways in cancer.癌症中的微小RNA生物合成途径。
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Identification of miR-26 as a key mediator of estrogen stimulated cell proliferation by targeting CHD1, GREB1 and KPNA2.鉴定 miR-26 作为雌激素刺激细胞增殖的关键介质,通过靶向 CHD1、GREB1 和 KPNA2。
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