Hsa-miR-210-3p expression in breast cancer and its putative association with worse outcome in patients treated with Docetaxel


Por: Pasculli, B, Barbano, R, Rendina, M, Fontana, A, Copetti, M, Mazza, T, Valori, VM, Morritti, M, Maiello, E, Graziano, P, Murgo, R, Fazio, VM, Esteller, M and Parrella, P

Publicada: 17 oct 2019
Categoría: Multidisciplinary

Resumen:
MicroRNA-210-3p is the most prominent hypoxia regulated microRNA, and it has been found significantly overexpressed in different human cancers. We performed the expression analysis of miR-210-3p in a retrospective cohort of breast cancer patients with a median follow-up of 76 months (n = 283). An association between higher levels of miR-210-3p and risk of disease progression (HR: 2.13, 95%CI: 1.33-3.39, P= 0.002) was found in the subgroup of patients treated with Epirubicin and Cyclophosphamide followed by Docetaxel. Moreover, a cut off value of 20.966 established by ROC curve analyses allowed to discriminate patients who developed distant metastases with an accuracy of 85% at 3- (AUC: 0.870, 95%CI: 0.690-1.000) and 83% at 5-years follow up (AUC: 0.832, 95%CI: 0.656-1.000). Whereas the accuracy in discriminating patients who died for the disease was of 79.6% at both 5- (AUC: 0.804, 95%CI: 0.517-1.000) and 10-years (AUC: 0.804. 95%CI: 0.517-1.000) follow-up. In silico analysis of miR-210-3p and Docetaxel targets provided evidence for a putative molecular cross-talk involving microtubule regulation, drug efflux metabolism and oxidative stress response. Overall, our data point to the miR210-3p involvement in the response to therapeutic regimens including Docetaxel in sequential therapy with anthracyclines, suggesting it may represent a predictive biomarker in breast cancer patients.

Filiaciones:
Pasculli, B:
 Fdn IRCCS Casa Sollievo Sofferenza, Lab Oncol, San Giovanni Rotondo, FG, Italy

Barbano, R:
 Fdn IRCCS Casa Sollievo Sofferenza, Lab Oncol, San Giovanni Rotondo, FG, Italy

Rendina, M:
 Fdn IRCCS Casa Sollievo Sofferenza, Lab Oncol, San Giovanni Rotondo, FG, Italy

Fontana, A:
 Fdn IRCCS Casa Sollievo Sofferenza, UO Biostat, San Giovanni Rotondo, FG, Italy

Copetti, M:
 Fdn IRCCS Casa Sollievo Sofferenza, UO Biostat, San Giovanni Rotondo, FG, Italy

Mazza, T:
 Fdn IRCCS Casa Sollievo Sofferenza, Bioinformat Unit, San Giovanni Rotondo, FG, Italy

Valori, VM:
 Fdn IRCCS Casa Sollievo Sofferenza, UO Oncol, San Giovanni Rotondo, FG, Italy

Morritti, M:
 Fdn IRCCS Casa Sollievo Sofferenza, UO Oncol, San Giovanni Rotondo, FG, Italy

Maiello, E:
 Fdn IRCCS Casa Sollievo Sofferenza, UO Oncol, San Giovanni Rotondo, FG, Italy

Graziano, P:
 Fdn IRCCS Casa Sollievo Sofferenza, UO Anat Patol, San Giovanni Rotondo, FG, Italy

Murgo, R:
 Fdn IRCCS Casa Sollievo Sofferenza, UO Chirurg Senol, San Giovanni Rotondo, FG, Italy

Fazio, VM:
 Fdn IRCCS Casa Sollievo Sofferenza, Lab Oncol, San Giovanni Rotondo, FG, Italy

:
 Bellvitge Biomed Biomed Res Inst IDIBELL, Canc Epigenet & Biol Program PEBC, Barcelona, Catalonia, Spain

 Ctr Invest Biomed Red Canc CIBERONC, Madrid, Spain

 Josep Carreras Leukaemia Res Inst, Barcelona, Catalonia, Spain

 Univ Barcelona, Physiol Sci Dept, Sch Med & Hlth Sci, Barcelona, Catalonia, Spain

 ICREA, Barcelona, Catalonia, Spain

Parrella, P:
 Fdn IRCCS Casa Sollievo Sofferenza, Lab Oncol, San Giovanni Rotondo, FG, Italy
ISSN: 20452322





Scientific Reports
Editorial
Nature Publishing Group, HEIDELBERGER PLATZ 3, BERLIN, 14197, GERMANY, Reino Unido
Tipo de documento: Article
Volumen: 9 Número:
Páginas:
WOS Id: 000490702200028
ID de PubMed: 31624308
imagen Green Published, gold

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