TY - JOUR U1 - Zeitschriftenartikel, wissenschaftlich - begutachtet (reviewed) A1 - Schöndorf, Thomas A1 - Eisele, Lewin A1 - Göhring, Uwe-Jochen A1 - Valter, Markus M. A1 - Warm, Mathias A1 - Mallmann, Peter A1 - Becker, Martina A1 - Fechteler, Roland A1 - Weisshaar, Maria-Paz A1 - Hoopmann, Markus T1 - The V109G Polymorphism of the p27 Gene CDKN1B Indicates a Worse Outcome in Node-Negative Breast Cancer Patients JF - Tumor Biology N2 - Although p27 plays a central role in cell cycle regulation, its role in breast cancer prognosis is controversial. Furthermore, the p27 gene CDKN1B carries a polymorphism with unknown functional relevance. This study was designed to evaluate p27 expression and p27 genotyping with respect to early breast cancer prognosis. 279 patients with infiltrating metastasis-free breast cancer were included in this study. p27 expression was determined in tumor tissue specimens from 261 patients by immunohistochemistry. From 108 patients, the CDKN1B genotype was examined by PCR and subsequent direct sequencing. 55.2% of the tumors were considered p27 positive. p27 expression did not correlate with any of the established parameters except for nodal involvement but significantly correlated to prolonged disease-free survival. In 35% of the tumors analyzed, the CDKN1B gene showed a polymorphism at codon 109 (V109G). The V109G polymorphism correlated with greater nodal involvement. In the node-negative subgroup, V109G correlated significantly with a shortened disease-free survival. In conclusion, the determination of the CDKN1B genotype might be a powerful tool for the prognosis of patients with early breast cancer. KW - Breast cancer KW - CDKN1B KW - Chemotherapy KW - Node involvement KW - p27 KW - Polymorphism KW - Prognosis UN - https://nbn-resolving.org/urn:nbn:de:hbz:1044-opus-2219 SN - 1010-4283 SS - 1010-4283 U6 - https://doi.org/10.1159/000081396 DO - https://doi.org/10.1159/000081396 PM - 15627896 VL - 25 IS - 5-6 SP - 306 EP - 312 PB - Karger CY - Basel ER -