Clinical significance of NOB1 expression in breast infiltrating ductal carcinoma

被引:0
作者
Li, Xiao-Yu [1 ]
Luo, Qi-Feng [1 ]
Li, Jia [1 ]
Wei, Chuan-Kui [1 ]
Kong, Xiang-Jie [1 ]
Zhang, Jun-Feng [1 ]
Fang, Lin [1 ]
机构
[1] Tongji Univ, Dept Breast & Thyroid Surg, Shanghai Peoples Hosp 10, Shanghai 200072, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2013年 / 6卷 / 10期
基金
中国国家自然科学基金;
关键词
Breast cancer; NOB1; protein; immunohistochemistry; tissue microarray; 18S RIBOSOMAL-RNA; 26S PROTEASOME; CANCER; BIOGENESIS; RESISTANCE; CLEAVAGE; PATHWAY; 3'-END;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: NIN/RPN Binding protein 1 homologue (NOBp1), encoded by NOB1 gene, was reported to play an essential role in the oncogenesis and prognosis of carcinomas. We conducted a study to reveal its expression and clinical significance in breast infiltrating ductal carcinoma. Methods: To explore the relationship between NOB1 expression and the clinical TNM (cTNM), 162 patients who undergone surgery were involved in the study. Compared to healthy tissues, abnormal localization and higher level of NOB1 in tumor cells was observed by Immunohistochemistry staining. Real-time PCR and western-blotting verified the up-regulation of NOB1 in carcinoma individuals. Results: A significant correlation between high level of NOB1 and the T stage, lymph node metastasis and cTNM was shown. Furthermore, patients with higher level of NOB1 predicted a declined overall survival (OS). Notably, multivariate analyses by Cox's proportional hazard model revealed that expression of NOB1 was an independent prognostic factor in breast infiltrating ductal carcinoma. Conclusions: In summary, our present study clarify that the aberrant expression of NOB1 in breast infiltrating ductal carcinoma is possibly involved with tumorigenesis and development, and the NOB1 protein could act as a potential biomarker for prognosis assessment of breast infiltrating ductal carcinoma. Related mechanism is worthy of further investigation.
引用
收藏
页码:2137 / 2144
页数:8
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