Oncotarget

Research Papers:

Measuring plasma levels of three microRNAs can improve the accuracy for identification of malignant breast lesions in women with BI-RADS 4 mammography

Julia Alejandra Pezuk, Thiago Luiz Araujo Miller, José Luiz Barbosa Bevilacqua, Alfredo Carlos Simões Dornellas de Barro, Felipe Eduardo Martins de Andrade, Luiza Freire de Andrade e Macedo, Vera Aguilar, Amanda Natasha Menardo Claro, Anamaria Aranha Camargo, Pedro Alexandre Favoretto Galante _ and Luiz F. L. Reis

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Oncotarget. 2017; 8:83940-83948. https://doi.org/10.18632/oncotarget.20806

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Abstract

Julia Alejandra Pezuk1,*, Thiago Luiz Araujo Miller1,2,*, José Luiz Barbosa Bevilacqua1, Alfredo Carlos Simões Dornellas de Barros1, Felipe Eduardo Martins de Andrade1, Luiza Freire de Andrade e Macedo1, Vera Aguilar1, Amanda Natasha Menardo Claro1,3, Anamaria Aranha Camargo1, Pedro Alexandre Favoretto Galante1 and Luiz F. L. Reis1

1Hospital Sírio-Libanês, São Paulo, Brazil

2Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo, Brazil

3Current address: SulAmerica, São Paulo, Brazil

*These authors contributed equally to this work

Correspondence to:

Pedro Alexandre Favoretto Galante, email: [email protected]

Luiz F. L. Reis, email: [email protected]

Keywords: micro RNAs, breast cancer, BI-RADS, blood plasma, machine learning

Received: June 17, 2017     Accepted: July 25, 2017     Published: September 11, 2017

ABSTRACT

A BI-RADS category of 4 from a mammogram indicates suspicious breast lesions, which require core biopsies for diagnosis and have an approximately one third chance of being malignant. Human plasma contains many circulating microRNAs, and variations in their circulating levels have been associated with pathologies, including cancer. Here, we present a novel methodology to identify malignant breast lesions in women with BI-RADS 4 mammography. First, we used the miRNome array and qRT-PCR to define circulating microRNAs that were differentially represented in blood samples from women with breast tumor (BI-RADS 5 or 6) in comparison to controls (BI-RADS 1 or 2). Next, we used qRT-PCR to quantify the level of this circulating microRNAs in patients with mammograms presenting with BI-RADS category 4. Finally, we developed a machine learning method (Artificial Neural Network - ANN) that receives circulating microRNA levels and automatically classifies BI-RADS 4 breast lesions as malignant or benign. We identified a minimum set of three circulating miRNAs (miR-15a, miR-101 and miR-144) with altered levels in patients with breast cancer. These three miRNAs were quantified in plasma from 60 patients presenting biopsy-proven BI-RADS 4 lesions. Finally, we constructed a very efficient ANN that could correctly classify BI-RADS 4 lesions as malignant or benign with approximately 92.5% accuracy, 95% specificity and 88% sensibility. We believe that our strategy of using circulating microRNA and a machine learning method to classify BI-RADS 4 breast lesions is a non-invasive, non-stressful and valuable complementary approach to core biopsy in women with BI-RADS 4 lesions.


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PII: 20806