CCAT2, a novel long non-coding RNA in breast cancer: Expression study and clinical correlations
Oncotarget , Volume 4 - Issue 10 p. 1748- 1762
The clinical outcome of BC patients receiving the same treatment is known to vary considerably and thus, there is a compelling need to identify novel biomarkers that can select the patients that would benefit most from a given therapy and can predict the clinical outcome. The aim of this study was to determine the prognostic value of CCAT2, a novel long ncRNA recently characterized by our group and overlapping SNP rs6983267, in BC patients. We first evaluated by RT-qPCR and ISH the expression of CCAT2 in normal breast tissue and BC tissue and further analyzed CCAT2 expression in an independent set of 997 primary BC with regard to clinical, histological, pathological and other biological factors. Also, we explored the possibility of CCAT2 adding to the prognostic value of multivariate models that already included the traditional prognostic factors. Finally, we identified in in vitro models the impact of CCAT2 expression and SNP rs6983267 genotype on cell migration and chemoresistance. Our results revealed that although overexpressed in BCs in two out of three sets of patients, and having the highest expression in lymph node negative (LNN) disease, CCAT2 expression levels are informative solely for a subgroup of BC patients, namely for patients with LNP disease that have received adjuvant CMF chemotherapy. For this subgroup high levels of CCAT2 suggest the patients will not benefit from CMF containing adjuvant chemotherapy (shorter MFS and OS). Additionally, we found that CCAT2 upregulates cell migration and downregulates chemosensitivity to 5'FU in a rs6983267-independent manner.
|Breast cancer, CCAT2, Non coding RNA, Prognosis, Real-time PCR|
|Organisation||Department of Medical Oncology|
Redis, R.S, Sieuwerts, A.M, Look, M.P, Tudoran, O, Ivan, C, Spizzo, R, … Calin, G.A. (2013). CCAT2, a novel long non-coding RNA in breast cancer: Expression study and clinical correlations. Oncotarget, 4(10), 1748–1762. Retrieved from http://hdl.handle.net/1765/85102