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      A genetic variant in microRNA-146a is associated with sporadic breast cancer in a Southern Brazilian Population

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          Abstract

          MicroRNAs (miRNAs) play an essential role in gene expression and affect the development of tumours, including breast cancer (BC). Polymorphisms in miRNA genes can affect the interaction of miRNAs with their target messenger RNA by interfering, creating or disrupting target sites. The single nucleotide polymorphism (SNP) rs2910164, located in the seed region of miR146a, was shown to be associated with BC among different populations. In the present study, we investigated whether rs2910164 is associated with BC in 326 patients and 411 controls from a Brazilian population of predominantly European ancestry. The presence of the allele rs2910164*C was associated with an increased risk of BC (OR=1.4, 95% CI=1.03-1.85, p = 0.03). We also analysed publicly available RNA-seq data to evaluate if miR146a is differentially expressed in different subtypes of BC. Genotyping was performed by polymerase chain reaction with sequence-specific primers (PCR-SSP). By leveraging public data from TCGA database, we analysed 461 patients and found that miR146a is significantly more expressed in BC than in non-tumor tissue (1.47 fold, p = 0.02) and is expressed to a greater degree in aggressive BC subtypes.

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          Genetic variation in microRNA networks: the implications for cancer research.

          Many studies have highlighted the role that microRNAs have in physiological processes and how their deregulation can lead to cancer. More recently, it has been proposed that the presence of single nucleotide polymorphisms in microRNA genes, their processing machinery and target binding sites affects cancer risk, treatment efficacy and patient prognosis. In reviewing this new field of cancer biology, we describe the methodological approaches of these studies and make recommendations for which strategies will be most informative in the future.
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            Properties of Sufficiency and Statistical Tests

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              Expression of microRNA-146 suppresses NF-kappaB activity with reduction of metastatic potential in breast cancer cells.

              Cancer cells often acquire a constitutively active nuclear factor-kappaB (NF-kappaB) program to promote survival, proliferation and metastatic potential by mechanisms that remain largely unknown. Extending observations from an immunologic setting, we demonstrate that microRNA-146a and microRNA-146b (miR-146a/b) when expressed in the highly metastatic human breast cancer cell line MDA-MB-231 function to negatively regulate NF-kappaB activity. Lentiviral-mediated expression of miR-146a/b significantly downregulated interleukin (IL)-1 receptor-associated kinase and TNF receptor-associated factor 6, two key adaptor/scaffold proteins in the IL-1 and Toll-like receptor signaling pathway, known to positively regulate NF-kappaB activity. Impaired NF-kappaB activity was evident from reduced phosphorylation of the NF-kappaB inhibitor IkappaBalpha, reduced NF-kappaB DNA-binding activity and suppressed expression of the NF-kappaB target genes IL-8, IL-6 and matrix metalloproteinase-9. Functionally, miR-146a/b-expressing MDA-MB-231 cells showed markedly impaired invasion and migration capacity relative to control cells. These findings implicate miR-146a/b as a negative regulator of constitutive NF-kappaB activity in a breast cancer setting and suggest that modulating miR-146a/b levels has therapeutic potential to suppress breast cancer metastases.
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                Author and article information

                Journal
                Genet Mol Biol
                Genet. Mol. Biol
                gmb
                Genetics and Molecular Biology
                Sociedade Brasileira de Genética
                1415-4757
                1678-4685
                03 February 2020
                2019
                : 42
                : 4
                : e20190278
                Affiliations
                [1 ]Universidade Federal do Paraná, Departamento de Genética, Curitiba, Paraná, Brazil.
                [2 ]Hospital Nossa Senhora das Graças, Centro de Doenças da Mama, Curitiba, Paraná, Brazil.
                Author notes
                Send correspondence to Maria de Souza Fonseca Ribeiro. Universidade Federal do Paraná, Departamento de Genética, Curitiba, Paraná, Brasil. E-mail: enilzeribeiro@ 123456gmail.com
                Current address: Department of Neurology, University of California, San Francisco, San Francisco, CA, United States.
                †† Current address: Molecular Epidemiology, Department of Biomedical Data Sciences, Leiden University Medical Centre. Leiden, Netherlands.
                Author information
                http://orcid.org/0000-0002-2194-4727
                Article
                00103
                10.1590/1678-4685-GMB-2019-0278
                7198002
                32142098
                3ab0fe50-46a8-4842-8d92-b9f22ed4331b
                Copyright © 2019, Sociedade Brasileira de Genética.

                License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License (type CC-BY), which permits unrestricted use, distribution and reproduction in any medium, provided the original article is properly cited.

                History
                : 18 August 2019
                : 21 November 2019
                Page count
                Figures: 2, Tables: 2, Equations: 0, References: 47
                Categories
                Human and Medical Genetics

                Molecular biology
                mirna polymorphism,mir146a,rs2910164,breast cancer,case-control study
                Molecular biology
                mirna polymorphism, mir146a, rs2910164, breast cancer, case-control study

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