MicroRNA-21 as an Indicator of Aggressive Phenotype in Breast Cancer

被引:33
作者
Ozgun, Alpaslan [1 ]
Karagoz, Bulent [1 ]
Bilgi, Oguz [1 ]
Tuncel, Tolga [1 ]
Baloglu, Huseyin [2 ]
Kandemir, Emin G. [1 ]
机构
[1] GATA Haydarpasa Training Hosp, Dept Med Oncol, Istanbul, Turkey
[2] GATA Haydarpasa Training Hosp, Dept Pathol, Istanbul, Turkey
来源
ONKOLOGIE | 2013年 / 36卷 / 03期
关键词
Breast cancer; microRNA; microRNA-21; TUMOR-SUPPRESSOR GENE; SMALL RNAS; EXPRESSION; METASTASIS; TARGETS; MIR-21; OVEREXPRESSION; INVASION; ELEGANS; CELLS;
D O I
10.1159/000348678
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The recently discovered microRNAs (miRNAs) are non-protein-coding, endogenous small RNAs. The aim of this study was to investigate the relationship between microRNA-21 (miR-21) and the clinicopathological features of breast cancer. Materials and Methods: Formalin-fixed, paraffin-embedded (FFPE) tissue samples were collected from 15 patients who had undergone surgery for primary breast cancer. The miR-21 expression levels in normal and cancer tissues were analyzed using real-time quantitative reverse transcriptase polymerase chain reaction (real-time qRT-PCR). The correlations between the miR-21 expression level and the stage of disease, the tumor size, lymph node involvement, hormone receptor status, human epidermal growth factor receptor 2 (HER2) status, and disease-free survival (DFS) were investigated. Results: The miR-21 expression levels were significantly higher in patients with stage Ill disease, patients with more than 3 axillary lymph node metastases and HER2-positive patients than in patients with stage I-II disease, patients with 1-3 axillary lymph node metastases and HER2-negative patients (p = 0.005, p = 0.037, and p = 0.014, respectively). Patients with high miR-21 expression level had a significantly shorter DFS than patients with low miR-21 expression level (median DFS: 18 and 56 months, respectively; p = 0.004). Conclusion: These results show that miR-21 is an indicator of an aggressive breast cancer phenotype and that it may be a new therapeutic target in the treatment of breast cancer in the future.
引用
收藏
页码:115 / 118
页数:6
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