1. Combined analysis of miR-200 family and its significance for breast cancer
- Author
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Maria Morritti, Valentina Melocchi, Andrea Fontana, Marina Castelvetere, Paolo Graziano, Sara Ravaioli, Raffaela Barbano, Vanna Maria Valori, Michelina Rendina, Massimiliano Copetti, Elisa Dama, Barbara Pasculli, Sara Bravaccini, Vito Michele Fazio, Paola Parrella, Luigi Ciuffreda, Evaristo Maiello, Manel Esteller, and Fabrizio Bianchi
- Subjects
0301 basic medicine ,Oncology ,Molecular biology ,Cancer specific survival ,Cohort Studies ,0302 clinical medicine ,Breast cancer ,Breast ,skin and connective tissue diseases ,Triple negative ,Cancer ,Multidisciplinary ,Biochemical markers ,Middle Aged ,Up-Regulation ,Gene Expression Regulation, Neoplastic ,030220 oncology & carcinogenesis ,Multigene Family ,Cohort ,Marcadors bioquímics ,Medicine ,Female ,Normal breast ,medicine.medical_specialty ,Epithelial-Mesenchymal Transition ,Science ,Breast Neoplasms ,Risk Assessment ,Article ,Disease-Free Survival ,Càncer de mama ,03 medical and health sciences ,Downregulation and upregulation ,Predictive Value of Tests ,Internal medicine ,Cell Line, Tumor ,microRNA ,medicine ,Biomarkers, Tumor ,Humans ,Neoplasm Staging ,business.industry ,Luminal b ,medicine.disease ,MicroRNAs ,030104 developmental biology ,Neoplasm Recurrence, Local ,business - Abstract
Fundació Carreras This work was supported by Italian Ministry of Health (MoH) TRANSCAN Joint Transnational Call (JTC) 2013 co-funded by the European Regional Development Fund, "A way of making Europe" RRC-2014-2354565, Italian Ministry of Health (MoH) "Ricerca Corrente 2019" and "5×1000″ voluntary contributions" and partially supported by Associazione Italiana Ricerca sul Cancro (AIRC) Project Code: 16747. While the molecular functions of miR-200 family have been deeply investigated, a role for these miRNAs as breast cancer biomarkers remains largely unexplored. In the attempt to clarify this, we profiled the miR-200 family members expression in a large cohort of breast cancer cases with a long follow-up (H-CSS cohort) and in TCGA-BRCA cohort. Overall, miR-200 family was found upregulated in breast tumors with respect to normal breast tissues while downregulated in more aggressive breast cancer molecular subtypes (i.e. Luminal B, HER2 and triple negative), consistently with their function as repressors of the epithelial-to-mesenchymal transition (EMT). In particular miR-141-3p was found differentially expressed in breast cancer molecular subtypes in both H-CSS and TCGA-BRCA cohorts, and the combined analysis of all miR-200 family members demonstrated a slight predictive accuracy on H-CSS cancer specific survival at 12 years (survival c-statistic: 0.646; 95%CI 0.538-0.754).
- Published
- 2021