Evidence map›Paper›PMID 42040804›Full record

ArticleGalen medical journal2022

Dysregulation of miR-577, miR-505-3p, miR-3682-3p, and miR-4661 in Breast Cancer Patients Based on Estrogen Receptor Status : Dysregulation of miRNAs in Breast Cancer Patients Based on ER Status.

Arman Moradi, Saeid Rahmani, Narges Jafarbeik Iravani, Rezvan Esmaeili, Seyed Javad Mowla, Keivan Majidzadeh-A

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Article in Galen medical journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Arman MoradiTasnim Biotechnology Center, Faculty of Medicine, AJA University of Medical Sciences, Tehran, Iran.
Saeid RahmaniDepartment of Computer Engineering, Sharif University of Technology, Tehran, Iran.
Narges Jafarbeik IravaniDepartment of Genetics, Breast Cancer Research Center, Motamed Cancer Institute, ACECR, Tehran, Iran.
Rezvan EsmaeiliDepartment of Genetics, Breast Cancer Research Center, Motamed Cancer Institute, ACECR, Tehran, Iran.
Seyed Javad MowlaDepartment of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.
Keivan Majidzadeh-ATasnim Biotechnology Center, Faculty of Medicine, AJA University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Breast cancer is one of the most common malignancies and the second leading cause of cancer-related death in women. Approximately 75% of all breast cancers are estrogen receptor-positive (ER+) and highly responsive to endocrine therapy. MicroRNAs (miRNAs) are short non-coding RNA with a pivotal role in mammal cells by regulating gene expression. Hence, this study aimed to evaluate the miRNAs expression in various breast cancer subtypes. Materials and Methods: In this study, after total RNA extraction and cDNA synthesis, expressions of miR-577, miR-505-3p, miR-3682-3p, and miR-4661-5p were investigated in 36 breast cancer samples of ER+ and ER- types and compared with 18 normal adjacent tissues by real-time polymerase chain reaction. Also, diagnostic values of miRNAs were determined based on receiver operating characteristic (ROC) by calculating the area under the curve (AUC). Results: Downregulation of miR-577 and miR-505-3p were detected in breast cancer samples, significantly in the ER+ subtype compared to ER- subtype (P0.001). Also, we showed upregulation of miR-3682-3p and miR-4661-5p in breast cancer tissues compared to normal tissues. Compared to the ER+ subtype, the miR-3682-3p expression significantly decreased in the ER- subtype (P0.001). However, there was no significant difference between ER+ and ER- subtypes in the term of miR-4661-5p (P˃0.05). The ROC analysis demonstrated that miR-577 and miR-505-3p have acceptable diagnostic values, and miR-3682-3p has a relatively proper diagnostic value in diagnosing breast cancer. Conclusion: Our results revealed that miR-577 and miR-505-3p could be used as biomarkers for the diagnosis of breast cancer, especially in ER+ subtype.

Indexed as

BiomarkersBreast CancerEstrogen ReceptorMicroRNAsReal-Time Polymerase Chain Reaction

Identifiers

PMID42040804
PMCPMC12335744

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