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Extracellular vesicles-associated miRNAs in triple-negative breast cancer: from tumor biology to clinical relevance.
Berti, Fernanda Costa Brandão; Tofolo, Maria Vitoria; Nunes-Souza, Emanuelle; Marchi, Rafael; Okano, Larissa Miyuki; Ruthes, Mayara; Rosolen, Daiane; Malheiros, Danielle; Fonseca, Aline Simoneti; Cavalli, Luciane Regina.
Afiliação
  • Berti FCB; Research Institute Pelé Pequeno Príncipe, Faculdades Pequeno Príncipe, Curitiba 80250-060, Brazil. Electronic address: fernanda.berti@pelepequenoprincipe.org.br.
  • Tofolo MV; Research Institute Pelé Pequeno Príncipe, Faculdades Pequeno Príncipe, Curitiba 80250-060, Brazil. Electronic address: maria.tofolo@aluno.fpp.edu.br.
  • Nunes-Souza E; Research Institute Pelé Pequeno Príncipe, Faculdades Pequeno Príncipe, Curitiba 80250-060, Brazil. Electronic address: emanuelle.souza@aluno.fpp.edu.br.
  • Marchi R; Research Institute Pelé Pequeno Príncipe, Faculdades Pequeno Príncipe, Curitiba 80250-060, Brazil. Electronic address: rafael.marchi@aluno.fpp.edu.br.
  • Okano LM; Research Institute Pelé Pequeno Príncipe, Faculdades Pequeno Príncipe, Curitiba 80250-060, Brazil. Electronic address: larissa.okano@aluno.fpp.edu.br.
  • Ruthes M; Research Institute Pelé Pequeno Príncipe, Faculdades Pequeno Príncipe, Curitiba 80250-060, Brazil. Electronic address: mayara.ruthes@aluno.fpp.edu.br.
  • Rosolen D; Research Institute Pelé Pequeno Príncipe, Faculdades Pequeno Príncipe, Curitiba 80250-060, Brazil. Electronic address: daiane.rosolen@pelepequenoprincipe.org.br.
  • Malheiros D; Department of Genetics, Universidade Federal do Paraná, Curitiba 80060-000, Brazil. Electronic address: dani_malheiros@ufpr.br.
  • Fonseca AS; Research Institute Pelé Pequeno Príncipe, Faculdades Pequeno Príncipe, Curitiba 80250-060, Brazil. Electronic address: aline.fonseca@pelepequenoprincipe.org.br.
  • Cavalli LR; Research Institute Pelé Pequeno Príncipe, Faculdades Pequeno Príncipe, Curitiba 80250-060, Brazil; Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20007, USA. Electronic address: luciane.cavalli@pelepequenoprincipe.org.br.
Life Sci ; 336: 122332, 2024 Jan 01.
Article em En | MEDLINE | ID: mdl-38070862
ABSTRACT
Breast cancer (BC), a heterogeneous group of diseases, is the most frequent type and the leading cause of cancer-related death among women worldwide. Tumor heterogeneity directly impacts cancer progression and treatment, as evidenced by the patients´ diverse prognosis and treatment responses across the distinct molecular subtypes. Triple-negative breast cancer (TNBC), which accounts for 10-20% of all diagnosed BC cases, is an aggressive BC subtype with a challenging prognosis. Current treatment options include systemic chemotherapy and/or target therapies based on PARP and PD-L1 inhibitors for eligible patients. MicroRNAs (miRNAs) are important regulatory non-coding RNAs (ncRNAs) in TNBC tumorigenesis. These molecules are present both intracellularly and released into biofluids, packaged into extracellular vesicles (EVs). Emerging evidence indicates that EVs-associated miRNAs (EVs-miRNAs), transferred from parental to recipient cells, are key mediators of cell-to-cell communication. Considering their stability and abundance in several biofluids, these molecules may reflect the epigenomic composition of their tumors of origin and contribute to mediate tumorigenesis, similar to their intracellular counterparts. This review provides the current knowledge on EVs-miRNAs in the TNBC subtype, focusing on their role in regulating mRNA targets involved in tumor phenotypes and their clinical relevance as promising biomarkers in liquid biopsies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs / Neoplasias de Mama Triplo Negativas / Vesículas Extracelulares Limite: Female / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs / Neoplasias de Mama Triplo Negativas / Vesículas Extracelulares Limite: Female / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article