<i>In Silico</i> Approach for the Definition of radiomiRNomic Signatures for Breast Cancer Differential Diagnosis

Personalized medicine relies on the integration and consideration of specific characteristics of the patient, such as tumor phenotypic and genotypic profiling. Background: Radiogenomics aim to integrate phenotypes from tumor imaging data with genomic data to discover genetic mechanisms underlying tu...

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Main Authors: Francesca Gallivanone, Claudia Cava, Fabio Corsi, Gloria Bertoli, Isabella Castiglioni
Format: Article
Language:English
Published: MDPI AG 2019-11-01
Series:International Journal of Molecular Sciences
Subjects:
mri
Online Access:https://www.mdpi.com/1422-0067/20/23/5825
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spelling doaj-76e9d8757a73431fb9a5c3ec20d2d70e2020-11-25T02:00:17ZengMDPI AGInternational Journal of Molecular Sciences1422-00672019-11-012023582510.3390/ijms20235825ijms20235825<i>In Silico</i> Approach for the Definition of radiomiRNomic Signatures for Breast Cancer Differential DiagnosisFrancesca Gallivanone0Claudia Cava1Fabio Corsi2Gloria Bertoli3Isabella Castiglioni4Institute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), Via F. Cervi 93, 20090 Segrate-Milan, Milan, ItalyInstitute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), Via F. Cervi 93, 20090 Segrate-Milan, Milan, ItalyLaboratory of Nanomedicine and Molecular Imaging, Istituti Clinici Scientifici Maugeri IRCCS, via Maugeri 4, 27100 Pavia, ItalyInstitute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), Via F. Cervi 93, 20090 Segrate-Milan, Milan, ItalyInstitute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), Via F. Cervi 93, 20090 Segrate-Milan, Milan, ItalyPersonalized medicine relies on the integration and consideration of specific characteristics of the patient, such as tumor phenotypic and genotypic profiling. Background: Radiogenomics aim to integrate phenotypes from tumor imaging data with genomic data to discover genetic mechanisms underlying tumor development and phenotype. Methods: We describe a computational approach that correlates phenotype from magnetic resonance imaging (MRI) of breast cancer (BC) lesions with microRNAs (miRNAs), mRNAs, and regulatory networks, developing a radiomiRNomic map. We validated our approach to the relationships between MRI and miRNA expression data derived from BC patients. We obtained 16 radiomic features quantifying the tumor phenotype. We integrated the features with miRNAs regulating a network of pathways specific for a distinct BC subtype. Results: We found six miRNAs correlated with imaging features in Luminal A (<i>miR-1537</i>, <i>-205</i>, <i>-335</i>, <i>-337</i>, <i>-452</i>, and <i>-99a</i>), seven miRNAs (<i>miR-142</i>, <i>-155</i>, <i>-190</i>, <i>-190b</i>, <i>-1910</i>, <i>-3617</i>, and <i>-429</i>) in HER2+, and two miRNAs (<i>miR-135b</i> and <i>-365-2</i>) in Basal subtype. We demonstrate that the combination of correlated miRNAs and imaging features have better classification power of Luminal A versus the different BC subtypes than using miRNAs or imaging alone. Conclusion: Our computational approach could be used to identify new radiomiRNomic profiles of multi-omics biomarkers for BC differential diagnosis and prognosis.https://www.mdpi.com/1422-0067/20/23/5825radiogenomicsradiomirnomicsbreast cancermagnetic resonance imagingmrimicrornas/mirnaspathwaysnetwork
collection DOAJ
language English
format Article
sources DOAJ
author Francesca Gallivanone
Claudia Cava
Fabio Corsi
Gloria Bertoli
Isabella Castiglioni
spellingShingle Francesca Gallivanone
Claudia Cava
Fabio Corsi
Gloria Bertoli
Isabella Castiglioni
<i>In Silico</i> Approach for the Definition of radiomiRNomic Signatures for Breast Cancer Differential Diagnosis
International Journal of Molecular Sciences
radiogenomics
radiomirnomics
breast cancer
magnetic resonance imaging
mri
micrornas/mirnas
pathways
network
author_facet Francesca Gallivanone
Claudia Cava
Fabio Corsi
Gloria Bertoli
Isabella Castiglioni
author_sort Francesca Gallivanone
title <i>In Silico</i> Approach for the Definition of radiomiRNomic Signatures for Breast Cancer Differential Diagnosis
title_short <i>In Silico</i> Approach for the Definition of radiomiRNomic Signatures for Breast Cancer Differential Diagnosis
title_full <i>In Silico</i> Approach for the Definition of radiomiRNomic Signatures for Breast Cancer Differential Diagnosis
title_fullStr <i>In Silico</i> Approach for the Definition of radiomiRNomic Signatures for Breast Cancer Differential Diagnosis
title_full_unstemmed <i>In Silico</i> Approach for the Definition of radiomiRNomic Signatures for Breast Cancer Differential Diagnosis
title_sort <i>in silico</i> approach for the definition of radiomirnomic signatures for breast cancer differential diagnosis
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2019-11-01
description Personalized medicine relies on the integration and consideration of specific characteristics of the patient, such as tumor phenotypic and genotypic profiling. Background: Radiogenomics aim to integrate phenotypes from tumor imaging data with genomic data to discover genetic mechanisms underlying tumor development and phenotype. Methods: We describe a computational approach that correlates phenotype from magnetic resonance imaging (MRI) of breast cancer (BC) lesions with microRNAs (miRNAs), mRNAs, and regulatory networks, developing a radiomiRNomic map. We validated our approach to the relationships between MRI and miRNA expression data derived from BC patients. We obtained 16 radiomic features quantifying the tumor phenotype. We integrated the features with miRNAs regulating a network of pathways specific for a distinct BC subtype. Results: We found six miRNAs correlated with imaging features in Luminal A (<i>miR-1537</i>, <i>-205</i>, <i>-335</i>, <i>-337</i>, <i>-452</i>, and <i>-99a</i>), seven miRNAs (<i>miR-142</i>, <i>-155</i>, <i>-190</i>, <i>-190b</i>, <i>-1910</i>, <i>-3617</i>, and <i>-429</i>) in HER2+, and two miRNAs (<i>miR-135b</i> and <i>-365-2</i>) in Basal subtype. We demonstrate that the combination of correlated miRNAs and imaging features have better classification power of Luminal A versus the different BC subtypes than using miRNAs or imaging alone. Conclusion: Our computational approach could be used to identify new radiomiRNomic profiles of multi-omics biomarkers for BC differential diagnosis and prognosis.
topic radiogenomics
radiomirnomics
breast cancer
magnetic resonance imaging
mri
micrornas/mirnas
pathways
network
url https://www.mdpi.com/1422-0067/20/23/5825
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