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乳腺癌中miR-126的表达水平及激素受体相关性评估

Evaluation of the Expression Level and Hormone Receptor Association of miR-126 in Breast Cancer.

作者信息

Rouigari Maedeh, Dehbashi Moein, Tabatabaeian Hossein, Ghaedi Kamran, Mohammadynejad Parisa, Azadeh Mansoureh

机构信息

Department of Biology, Faculty of Basic Sciences, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran.

2Division of Genetics, Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran.

出版信息

Indian J Clin Biochem. 2019 Oct;34(4):451-457. doi: 10.1007/s12291-018-0766-6. Epub 2018 Jun 16.

Abstract

Breast cancer is a major cause of cancer-related death in women worldwide. miRNAs are new players of breast tumorigenesis, used as diagnostic and prognostic biomarkers. Among various miRNAs, miR-126 has been proposed to have a tumor suppressive role in HER2 positive cancer. However, to have a better understanding of its role, further validation is required. The aim of this study was evaluating miR-126 expression level in breast cancer tissues and investigating its potential association with HER2, estrogen and progesterone receptors. miR-126 expression level was measured in 108 specimens including 78 malignant and 30 normal samples using RT-qPCR. The outcome was statistically analyzed. In silico studies were performed to find the potential mechanism of action, through which miR-126 imposes its function. Down-regulation of miR-126 was observed in tumor samples, as compared to the matched normal tissues. Down-regulation of miR-126 was also associated significantly with the absence of estrogen receptor in malignant samples. No association between miR-126 expression and HER2 status was observed. Our in silico analyses showed the possible role of Crk, PIK and Ras proto-oncogenes in breast cancer tumorigenesis. miR-126 is significantly down-regulated in breast cancer tissues. Statistically, it showed no correlation with HER2 positivity. However, the association between lower miR-126 and estrogen receptor negativity was observed.

摘要

乳腺癌是全球女性癌症相关死亡的主要原因。微小RNA(miRNAs)是乳腺肿瘤发生的新参与者,可作为诊断和预后生物标志物。在各种miRNAs中,miR-126被认为在HER2阳性癌症中具有肿瘤抑制作用。然而,为了更好地了解其作用,还需要进一步验证。本研究的目的是评估乳腺癌组织中miR-126的表达水平,并研究其与HER2、雌激素和孕激素受体的潜在关联。使用RT-qPCR在108个样本中测量miR-126的表达水平,其中包括78个恶性样本和30个正常样本。对结果进行统计学分析。进行了计算机模拟研究以寻找miR-126发挥其功能的潜在作用机制。与匹配的正常组织相比,在肿瘤样本中观察到miR-126下调。miR-126下调也与恶性样本中雌激素受体的缺失显著相关。未观察到miR-126表达与HER2状态之间的关联。我们的计算机模拟分析显示了Crk、PIK和Ras原癌基因在乳腺癌肿瘤发生中的可能作用。miR-126在乳腺癌组织中显著下调。统计学上,它与HER2阳性无相关性。然而,观察到较低的miR-126与雌激素受体阴性之间的关联。

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本文引用的文献

1
miR-581-Related Single Nucleotide Polymorphism, rs2641726, Located in MUC4 Gene, is Associated with Gastric Cancer Incidence.
Indian J Clin Biochem. 2019 Jul;34(3):347-351. doi: 10.1007/s12291-018-0751-0. Epub 2018 Apr 10.
2
Deregulation of miR-126-3p in basal-like breast cancers stroma and its clinical significance.
Pathol Res Pract. 2017 Aug;213(8):922-928. doi: 10.1016/j.prp.2017.05.010. Epub 2017 May 31.
3
The association between rs1972820 and the risk of breast cancer in Isfahan population.
J Cancer Res Ther. 2017 Jan-Mar;13(1):26-32. doi: 10.4103/0973-1482.183202.
4
Cooverexpression of EpCAM and c-myc genes in malignant breast tumours.
J Genet. 2017 Mar;96(1):109-118. doi: 10.1007/s12041-017-0748-0.
8
miRpower: a web-tool to validate survival-associated miRNAs utilizing expression data from 2178 breast cancer patients.
Breast Cancer Res Treat. 2016 Dec;160(3):439-446. doi: 10.1007/s10549-016-4013-7. Epub 2016 Oct 15.
9
rs11895168 C allele and the increased risk of breast cancer in Isfahan population.
Breast. 2016 Aug;28:89-94. doi: 10.1016/j.breast.2016.05.007. Epub 2016 Jun 1.
10
miRTarBase 2016: updates to the experimentally validated miRNA-target interactions database.
Nucleic Acids Res. 2016 Jan 4;44(D1):D239-47. doi: 10.1093/nar/gkv1258. Epub 2015 Nov 20.

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