Παρακαλώ χρησιμοποιήστε αυτό το αναγνωριστικό για να παραπέμψετε ή να δημιουργήσετε σύνδεσμο προς αυτό το τεκμήριο:
https://hdl.handle.net/10442/17539
Εξειδίκευση τύπου : | Άρθρο σε επιστημονικό περιοδικό |
Τίτλος: | Estrogen receptors β1 and β2 are associated with distinct responses of estrogen receptor α-positive breast carcinoma to adjuvant endocrine therapy |
Δημιουργός/Συγγραφέας: | Dhimolea E. Tiniakos D.G. Chantzi N.T. Goutas N. Vassilaros S.D. [EL] Μήτσιου, Δήμητρα[EN] Mitsiou, Dimitra J. [EL] Αλέξης, Μιχαήλ Ν.[EN] Alexis, Michael N. |
Εκδότης: | Elsevier Ireland Ltd |
Ημερομηνία: | 2015 |
Γλώσσα: | Αγγλικά |
ISSN: | 0304-3835 |
DOI: | 10.1016/j.canlet.2014.12.022 |
Άλλο: | PubMed ID: 25524554 |
Περίληψη: | Our purpose was to assess whether and how ERβ1 and/or ERβ2 expression status could predict response of early stage ERα-positive breast carcinoma to adjuvant endocrine therapy (AET). ERβ1 and ERβ2 expression were determined using immunohistochemistry. ERβ1- and ERβ2-positivity were derived from receiver operating characteristic analysis and the median percentage of immunostained tumor cells, respectively. Patients with recurrent disease were grouped according to whether they relapsed within 4 years or after 4 years from surgery. The predictive significance of ERβ1 and ERβ2 was determined using Kaplan-Meier survival analysis and Cox proportional hazards regression analysis. ERβ1-positivity in the first-4-year relapse patient group was lower and ERβ2-positivity in the post-4-year relapse group was higher compared with no-relapse group. ERβ1-positivity was associated with lower tumor size and longer first-4-year disease-free survival, while ERβ2-positivity was associated with shorter post-4-year disease-free survival. Cox multivariate analysis including ERβ1, ERβ2 and established clinico-pathological variables showed that ERβ1-positivity was an independent predictor of lower first-4-year risk of relapse. Thus, low ERβ1 expression and high ERβ2 expression are markers for identification of AET-treated ERα-positive breast carcinoma patients at risk of early and late relapse, respectively. |
Τίτλος πηγής δημοσίευσης: | Cancer Letters |
Τόμος/Κεφάλαιο: | 358 |
Τεύχος: | 1 |
Σελίδες: | 37-42 |
Θεματική Κατηγορία: | [EL] Βιοχημεία[EN] Biochemistry [EL] Θεραπευτική. Φαρμακολογία[EN] Therapeutics.Pharmacology |
Λέξεις-Κλειδιά: | Breast carcinoma Endocrine therapy ERβ1 ERβ2 Immunohistochemistry |
Αξιολόγηση από ομότιμους (peer reviewed): | Ναι |
Κάτοχος πνευματικών δικαιωμάτων: | © 2014 Elsevier Ireland Ltd. |
Σημειώσεις: | THALES 85355; 03ED644. This study was supported by EU Social Fund and Greek national funds through the Operational Program ‘Education and Lifelong Learning’ (Project THALES 85355 ) and the NSRF Research Funding Program (Project 03ED644 ). |
Εμφανίζεται στις συλλογές: | Ινστιτούτο Χημικής Βιολογίας - Επιστημονικό έργο
|
Αρχεία σε αυτό το τεκμήριο:
Το πλήρες κείμενο αυτού του τεκμηρίου δεν διατίθεται προς το παρόν από τον ΗΛΙΟ.