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miR‐99a‐5p modulates doxorubicin resistance via the COX‐2/ABCG2 axis in triple‐negative breast cancer: from the discovery to in vivo studies

Abbreviations ABCG2 ATP-binding cassette subfamily G member 2 ALT alanine transaminase AST aspartate aminotransferase ATCC American Type Culture Collection BC breast cancer BET Brunauer−Emmett−Teller BJH Barret-Joyner-Halenda CI confidence interval COX-2 cyclooxygenase-2 CRE creatinine CTAB Cetyltri...

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Published in:Cancer communications (London, England) England), 2022-12, Vol.42 (12), p.1412-1416
Main Authors: Garrido‐Cano, Iris, Adam‐Artigues, Anna, Lameirinhas, Ana, Blandez, Juan F., Candela‐Noguera, Vicente, Rojo, Federico, Zazo, Sandra, Madoz‐Gúrpide, Juan, Lluch, Ana, Bermejo, Begoña, Sancenón, Felix, Cejalvo, Juan Miguel, Martínez‐Máñez, Ramón, Eroles, Pilar
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cited_by cdi_FETCH-LOGICAL-c5112-5077c7ef9b8b76dc8b3bff387e9799dfbc0ee9d8a510eee85c54c0f70bb692c33
cites cdi_FETCH-LOGICAL-c5112-5077c7ef9b8b76dc8b3bff387e9799dfbc0ee9d8a510eee85c54c0f70bb692c33
container_end_page 1416
container_issue 12
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container_title Cancer communications (London, England)
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creator Garrido‐Cano, Iris
Adam‐Artigues, Anna
Lameirinhas, Ana
Blandez, Juan F.
Candela‐Noguera, Vicente
Rojo, Federico
Zazo, Sandra
Madoz‐Gúrpide, Juan
Lluch, Ana
Bermejo, Begoña
Sancenón, Felix
Cejalvo, Juan Miguel
Martínez‐Máñez, Ramón
Eroles, Pilar
description Abbreviations ABCG2 ATP-binding cassette subfamily G member 2 ALT alanine transaminase AST aspartate aminotransferase ATCC American Type Culture Collection BC breast cancer BET Brunauer−Emmett−Teller BJH Barret-Joyner-Halenda CI confidence interval COX-2 cyclooxygenase-2 CRE creatinine CTAB Cetyltrimethylammonium bromide DAPI 4',6-diamidino-2-phenylindole DLS dynamic light scattering DRFS distant-relapse free survival FDR false discovery rate FTIR Fourier-transform infrared GEO Gene Expression Omnibus H&E hematoxylin and eosin H&E hematoxylin and eosin HA hyaluronic acid HR hazard ratio IC50 half-maximal inhibitory concentration ICP-MS inductively coupled plasma mass spectrometry METABRIC Molecular Taxonomy of Breast Cancer International Consortium MFI mean fluorescence intensity MSNs mesoporous silica nanoparticles myh7 Myosin Heavy Chain 7 NCBI National Center for Biotechnology Information OS overall survival PEI polyethyleneimine PTFE polytetrafluoroethylene PXRD Powder X-ray diffraction qRT-PCR quantitative real-time PCR RIPA radioimmunoprecipitation RNU43 U43 Small Nuclear RNA SAED selected area electron diffraction SD standard deviation SDS-PAGE sodium dodecyl sulfate–polyacrylamide gel electrophoresis SEM standard error of the mean siRNAs short interfering RNAs TCGA The Cancer Genome Atlas TEM transmission electron microscopy TEOS tetraethylorthosilicate TGA thermogravimetric analysis TMAH tetramethylammonium hydroxide solution TNBC triple-negative breast cancer URE urea UTR untranslated region Dear Editor, Breast cancer (BC) is the most commonly diagnosed cancer and the fifth cause of cancer-related death worldwide [ 1]. In this context, microRNAs have emerged as potential therapeutic targets to overcome therapy resistance [ 4]. [...]we aimed to elucidate the molecular mechanisms underlying resistance to doxorubicin, one of the most effective chemotherapeutic agents used in BC. Additionally, its association with overall survival (OS) was assessed in the Molecular Taxonomy of Breast Cancer International Consortium (METABRIC, n = 1262) and The Cancer Genome Atlas (TCGA) cohorts (n = 1062), which confirmed that low miR-99a-5p expression was associated with poor prognosis (Supplementary Figure S1D-E). [...]we hypothesized that miR-99a-5p could increase doxorubicin sensitivity. miR-99a-5p was described to increase sensitivity to radiation and cisplatin [ 6, 7], but its role in doxorubicin resistance was still unexplored. [...]we hypothesized that ABCG2
doi_str_mv 10.1002/cac2.12352
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In this context, microRNAs have emerged as potential therapeutic targets to overcome therapy resistance [ 4]. [...]we aimed to elucidate the molecular mechanisms underlying resistance to doxorubicin, one of the most effective chemotherapeutic agents used in BC. Additionally, its association with overall survival (OS) was assessed in the Molecular Taxonomy of Breast Cancer International Consortium (METABRIC, n = 1262) and The Cancer Genome Atlas (TCGA) cohorts (n = 1062), which confirmed that low miR-99a-5p expression was associated with poor prognosis (Supplementary Figure S1D-E). [...]we hypothesized that miR-99a-5p could increase doxorubicin sensitivity. miR-99a-5p was described to increase sensitivity to radiation and cisplatin [ 6, 7], but its role in doxorubicin resistance was still unexplored. 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In this context, microRNAs have emerged as potential therapeutic targets to overcome therapy resistance [ 4]. [...]we aimed to elucidate the molecular mechanisms underlying resistance to doxorubicin, one of the most effective chemotherapeutic agents used in BC. Additionally, its association with overall survival (OS) was assessed in the Molecular Taxonomy of Breast Cancer International Consortium (METABRIC, n = 1262) and The Cancer Genome Atlas (TCGA) cohorts (n = 1062), which confirmed that low miR-99a-5p expression was associated with poor prognosis (Supplementary Figure S1D-E). [...]we hypothesized that miR-99a-5p could increase doxorubicin sensitivity. miR-99a-5p was described to increase sensitivity to radiation and cisplatin [ 6, 7], but its role in doxorubicin resistance was still unexplored. 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In this context, microRNAs have emerged as potential therapeutic targets to overcome therapy resistance [ 4]. [...]we aimed to elucidate the molecular mechanisms underlying resistance to doxorubicin, one of the most effective chemotherapeutic agents used in BC. Additionally, its association with overall survival (OS) was assessed in the Molecular Taxonomy of Breast Cancer International Consortium (METABRIC, n = 1262) and The Cancer Genome Atlas (TCGA) cohorts (n = 1062), which confirmed that low miR-99a-5p expression was associated with poor prognosis (Supplementary Figure S1D-E). [...]we hypothesized that miR-99a-5p could increase doxorubicin sensitivity. miR-99a-5p was described to increase sensitivity to radiation and cisplatin [ 6, 7], but its role in doxorubicin resistance was still unexplored. [...]we hypothesized that ABCG2 could be a downstream target of miR-99a-5p through COX-2.</abstract><cop>United States</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>35997029</pmid><doi>10.1002/cac2.12352</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-1211-473X</orcidid><oa>free_for_read</oa></addata></record>
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source Open Access: PubMed Central; Wiley Online Library website; ProQuest Publicly Available Content database
subjects Apoptosis
ATP Binding Cassette Transporter, Subfamily G, Member 2 - genetics
Breast cancer
Cancer therapies
Consortia
Cyclooxygenase 2
Doxorubicin - pharmacology
Drug resistance
Flow cytometry
Gene expression
Gene Expression Regulation, Neoplastic
Genomes
Humans
Hyaluronic acid
Letter to the Editor
Letters to the Editor
Medical prognosis
MicroRNAs
MicroRNAs - genetics
Microscopy
Nanoparticles
Neoplasm Proteins
Taxonomy
Triple Negative Breast Neoplasms - drug therapy
Triple Negative Breast Neoplasms - genetics
title miR‐99a‐5p modulates doxorubicin resistance via the COX‐2/ABCG2 axis in triple‐negative breast cancer: from the discovery to in vivo studies
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