» Articles » PMID: 24641801

MicroRNA-484 is More Highly Expressed in Serum of Early Breast Cancer Patients Compared to Healthy Volunteers

Overview
Journal BMC Cancer
Publisher Biomed Central
Specialty Oncology
Date 2014 Mar 20
PMID 24641801
Citations 46
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Previous studies have profiled breast cancer compared to normal breast tissue and identified differentially expressed microRNAs (miRNAs). These miRNAs are then assessed in serum of breast cancer patients compared to healthy volunteers. MiRNAs in serum however do not always reflect what is in tissue and important serum miRNAs may be missed. PCR arrays were therefore performed on serum samples from breast cancer patients compared to healthy volunteers with the aim of identifying circulating miRNAs that are more highly expressed in serum from early breast cancer patients compared to controls.

Methods: Taqman low density array (TLDA) cards were used to profile serum miRNAs in a discovery cohort of serum from 39 early breast cancer patients compared to 10 healthy volunteers. The results were confirmed in a validation cohort of serum from 98 early breast cancer patients compared to 25 healthy volunteers using customized qPCR plates.

Results: Seventeen miRNAs were found to have significantly higher levels in breast cancer serum compared to serum of healthy volunteers in the discovery cohort. Fourteen of these miRNAs were studied in the validation cohort and serum miR-484 was found to be at a significantly higher level in breast cancer serum compared to healthy volunteers.

Conclusion: In this study, we found that miR-484 is significantly differentially expressed in serum of early breast cancer patients compared to healthy volunteers. We did not however find any correlation between miR-484 levels with histopathological parameters of the breast cancers. With further studies, miR-484 may prove useful as an adjunct to mammography for detection of early breast cancer.

Citing Articles

A machine learning model revealed that exosome small RNAs may participate in the development of breast cancer through the chemokine signaling pathway.

Mo J, Li X, Lei L, Peng J, Liang X, Zhou H BMC Cancer. 2024; 24(1):1435.

PMID: 39574053 PMC: 11580650. DOI: 10.1186/s12885-024-13173-x.


Tumor-derived EV miRNA signatures surpass total EV miRNA in supplementing mammography for precision breast cancer diagnosis.

Kim Y, Kim J, Moon S, Lee H, Lee S, Kim J Theranostics. 2024; 14(17):6587-6604.

PMID: 39479442 PMC: 11519808. DOI: 10.7150/thno.99245.


Liquid biopsy utilizing miRNA in patients with advanced breast cancer treated with cyclin‑dependent kinase 4/6 inhibitors.

Kubeczko M, Tudrej P, Tyszkiewicz T, Krzywon A, Oczko-Wojciechowska M, Jarzab M Oncol Lett. 2024; 27(4):181.

PMID: 38464342 PMC: 10921259. DOI: 10.3892/ol.2024.14314.


Identifying MicroRNAs Suitable for Detection of Breast Cancer: A Systematic Review of Discovery Phases Studies on MicroRNA Expression Profiles.

Padroni L, De Marco L, Fiano V, Milani L, Marmiroli G, Giraudo M Int J Mol Sci. 2023; 24(20).

PMID: 37894794 PMC: 10607026. DOI: 10.3390/ijms242015114.


New insights of miRNA molecular mechanisms in breast cancer brain metastasis and therapeutic targets.

Hussen B, Abdullah K, Abdullah S, Majeed N, Mohamadtahr S, Rasul M Noncoding RNA Res. 2023; 8(4):645-660.

PMID: 37818447 PMC: 10560790. DOI: 10.1016/j.ncrna.2023.09.003.


References
1.
Iorio M, Ferracin M, Liu C, Veronese A, Spizzo R, Sabbioni S . MicroRNA gene expression deregulation in human breast cancer. Cancer Res. 2005; 65(16):7065-70. DOI: 10.1158/0008-5472.CAN-05-1783. View

2.
Heneghan H, Miller N, Lowery A, Sweeney K, Newell J, Kerin M . Circulating microRNAs as novel minimally invasive biomarkers for breast cancer. Ann Surg. 2010; 251(3):499-505. DOI: 10.1097/SLA.0b013e3181cc939f. View

3.
Gilad S, Meiri E, Yogev Y, Benjamin S, Lebanony D, Yerushalmi N . Serum microRNAs are promising novel biomarkers. PLoS One. 2008; 3(9):e3148. PMC: 2519789. DOI: 10.1371/journal.pone.0003148. View

4.
Wang F, Zheng Z, Guo J, Ding X . Correlation and quantitation of microRNA aberrant expression in tissues and sera from patients with breast tumor. Gynecol Oncol. 2010; 119(3):586-93. DOI: 10.1016/j.ygyno.2010.07.021. View

5.
Yan L, Huang X, Shao Q, Huang M, Deng L, Wu Q . MicroRNA miR-21 overexpression in human breast cancer is associated with advanced clinical stage, lymph node metastasis and patient poor prognosis. RNA. 2008; 14(11):2348-60. PMC: 2578865. DOI: 10.1261/rna.1034808. View