Carregant...
Miniatura

Tipus de document

Article

Versió

Versió publicada

Data de publicació

Llicència de publicació

cc-by (c) Fontana, Andrea et al., 2021
Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/177003

Combined analysis of miR-200 family and its significance for breast cancer

Títol de la revista

Director/Tutor

ISSN de la revista

Títol del volum

Resum

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).

Citació

Citació

FONTANA, Andrea, BARBANO, Raffaela, DAMA, Elisa, PASCULLI, Barbara, RENDINA, Michelina, MORRITTI, Maria grazia, MELOCCHI, Valentina, CASTELVETERE, Marina, VALORI, Vanna maria, RAVAIOLI, Sara, BRAVACCINI, Sara, CIUFFREDA, Luigi, GRAZIANO, Paolo, MAIELLO, Evaristo, COPETTI, Massimiliano, FAZIO, Vito michele, ESTELLER, Manel, BIANCHI, Fabrizio, PARRELLA, Paola. Combined analysis of miR-200 family and its significance for breast cancer. _Scientific Reports_. 2021. Vol. 11, núm. 1, pàgs. 2980. [consulta: 24 de gener de 2026]. ISSN: 2045-2322. [Disponible a: https://hdl.handle.net/2445/177003]

Exportar metadades

JSON - METS

Compartir registre