Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Novel hyper methylated miRNA genes and its potential targets in breast cancer

4th World Congress on Breast Pathology and Cancer Diagnosis

Eleonora A Braga

Institute of General Pathology and Pathophysiology, Russia

Posters & Accepted Abstracts: Breast Can Curr Res

DOI: 10.4172/2572-4118-C1-009

Abstract
Epigenetic mechanisms including DNA methylation and interaction between miRNAs and mRNAs are the most dynamic mechanisms of genes deregulation in cancer. The aim of the study was to identify novel miRNA genes, regulated by DNA methylation, and target genes involved in the apoptosis, in breast cancer (BC). We used 58 paired (tumor/normal) BC samples, methylation-specific PCR, and quantitative PCR. Algorithms of miRWalk 2.0 database and the IBM SPSS statistics base 20 software package were used. We observed hyper methylation of 9 miRNA genes, and for the first time � of MIR-127, -132, -1258 and -193a, and hypo-methylation of MIR-191. Using qPCR, we established a strong correlation between promoter methylation and expression levels for 10 miRNA genes, demonstrating the functional importance of altered methylation patterns. A strong association between hyper methylation of MIR-127 and MIR-125b-1 and BC progression, particularly metastasis was found. The negative correlations were revealed between expression level alterations of 3 genes and 6 potential regulatory miRNAs for the following pairs: BCL2 � miR-124-3p, -212-3p, -24.2-5p; DAPK1�miR-127-5p, miR-9; RASSF1 (A)�miR-375 (Rs=-0.43 - -0.32, p�0.01, p�0.05). The results of transfection of MCF7 cell line with miR-124-3p duplex oligonucleotide analogues strengthened the hypothesis on the direct or indirect interaction of this miRNA with mRNA of the BCL2 gene. Thus, novel hyper methylated miRNA genes and potential interactions of DAPK1, BCL2, and RASSF1 (A) mRNAs with a number of miRNAs were identified that could be useful as markers and potential targets in combined BC therapy.
Biography

Eleonora A Braga has completed her PhD at Lomonosov Moscow State University, Bioorganic Chemistry Department. She has taken part in Russian Human Genome Project and HUGO. She was an Invited Principle Investigator at Karolinska Institute (Stockholm, Sweden, 1999-2000). She has completed her full Dr. of Biology Sc. at Engelhardt Institute of Molecular Biology in 2007. She is a head of Laboratory of Pathogenomics and Transcriptomics at Institute of General Pathology and Pathophysiology, Moscow, Russia. She has published more than 70 papers in reputed Journals.
 

Relevant Topics
Top