The abundance of the long intergenic non-coding RNA 01087 differentiates between luminal and triple-negative breast cancers and predicts patient outcome

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  • dc.contributor.author Palma, Fatima Domenica Elisa de
  • dc.contributor.author Monaco, Valentina del
  • dc.contributor.author Pol, Jonathan G.
  • dc.contributor.author Kremer, Margerie
  • dc.contributor.author D'Argenio, Valeria
  • dc.contributor.author Stoll, Gautier
  • dc.contributor.author Montanaro, Donatella
  • dc.contributor.author Uszczynska-Ratajczak, Barbara
  • dc.contributor.author Klein, Cecilia C.
  • dc.contributor.author Vlasova, Anna
  • dc.contributor.author Botti, Gerardo
  • dc.contributor.author D'Aiuto, Massimiliano
  • dc.contributor.author Baldi, Alfonso
  • dc.contributor.author Guigó Serra, Roderic
  • dc.contributor.author Kroemer, Guido
  • dc.contributor.author Maiuri, Maria Chiara
  • dc.contributor.author Salvatore, Francesco
  • dc.date.accessioned 2020-11-24T07:07:08Z
  • dc.date.available 2020-11-24T07:07:08Z
  • dc.date.issued 2020
  • dc.description.abstract The molecular complexity of human breast cancer (BC) renders the clinical management of the disease challenging. Long non-coding RNAs (lncRNAs) are promising biomarkers for BC patient stratification, early detection, and disease monitoring. Here, we identified the involvement of the long intergenic non-coding RNA 01087 (LINC01087) in breast oncogenesis. LINC01087 appeared significantly downregulated in triple-negative BCs (TNBCs) and upregulated in the luminal BC subtypes in comparison to mammary samples from cancer-free women and matched normal cancer pairs. Interestingly, deregulation of LINC01087 allowed to accurately distinguish between luminal and TNBC specimens, independently of the clinicopathological parameters, and of the histological and TP53 or BRCA1/2 mutational status. Moreover, increased expression of LINC01087 predicted a better prognosis in luminal BCs, while TNBC tumors that harbored lower levels of LINC01087 were associated with reduced relapse-free survival. Furthermore, bioinformatics analyses were performed on TNBC and luminal BC samples and suggested that the putative tumor suppressor activity of LINC01087 may rely on interferences with pathways involved in cell survival, proliferation, adhesion, invasion, inflammation and drug sensitivity. Altogether, these data suggest that the assessment of LINC01087 deregulation could represent a novel, specific and promising biomarker not only for the diagnosis and prognosis of luminal BC subtypes and TNBCs, but also as a predictive biomarker of pharmacological interventions.
  • dc.format.mimetype application/pdf
  • dc.identifier.citation De Palma FDE, Del Monaco V, Pol JG, Kremer M, D'Argenio V, Stoll G, Montanaro D, Uszczynska-Ratajczak B, Klein CC, Vlasova A, Botti G, D'Aiuto M, Baldi A, Guigó R, Kroemer G, Maiuri MC, Salvatore F. The abundance of the long intergenic non-coding RNA 01087 differentiates between luminal and triple-negative breast cancers and predicts patient outcome. Pharmacol Res. 2020 Nov;161:105249. DOI: 10.1016/j.phrs.2020.105249
  • dc.identifier.doi http://dx.doi.org/10.1016/j.phrs.2020.105249
  • dc.identifier.issn 1043-6618
  • dc.identifier.uri http://hdl.handle.net/10230/45878
  • dc.language.iso eng
  • dc.publisher Elsevier
  • dc.relation.ispartof Pharmacol Res. 2020 Nov;161:105249
  • dc.rights © 2020 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (https://creativecommons.org/licenses/by-nc-nd/4.0/)
  • dc.rights.accessRights info:eu-repo/semantics/openAccess
  • dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/4.0/
  • dc.subject.keyword Biomarker
  • dc.subject.keyword Breast cancer
  • dc.subject.keyword LINC01087
  • dc.subject.keyword Long non-coding RNA
  • dc.subject.keyword Luminal breast cancer
  • dc.subject.keyword Triple-negative breast cancer
  • dc.title The abundance of the long intergenic non-coding RNA 01087 differentiates between luminal and triple-negative breast cancers and predicts patient outcome
  • dc.type info:eu-repo/semantics/article
  • dc.type.version info:eu-repo/semantics/publishedVersion