Expression of aryl hydrocarbon receptor in relation to p53 status and clinicopathological parameters in breast cancer

被引:0
|
作者
Li, Zheng-Dong [1 ]
Wang, Kai [1 ]
Yang, Xin-Wei [2 ]
Zhuang, Zhi-Gang [1 ]
Wang, Jian-Jun [3 ]
Tong, Xiao-Wen [3 ]
机构
[1] Tongji Univ, Sch Med, Shanghai Matern & Infant Hosp 1, Shanghai 200040, Peoples R China
[2] Shanghai Univ TCM, Shanghai TCM Hosp, Shanghai 200071, Peoples R China
[3] Tongji Univ, Sch Med, Tongji Hosp, Shanghai 200092, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2014年 / 7卷 / 11期
关键词
AhR; breast cancer; tissue microarray; p53; immunohistochemistry; INHIBITOR PIFITHRIN-ALPHA; CELLS; GROWTH; CARCINOGENESIS; ACTIVATION; INVASION; ER;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aryl hydrocarbon receptor (AhR) is a ligand activated transcription factor implicated in multiple cellular processes and its expression has been shown to play a critical role in tumorigenesis. However, the role of AhR in tumorigenesis of breast cancer remains unclear. In the current study, we investigated the expression levels of AhR in breast lesions and assessing the correlation between AhR expression and clinicopathological variables using breast cancer tissue microarray. Meanwhile, 10 paired of fresh breast cancer and corresponding non-cancer samples were detected for AhR and p53 expression by Western blot, respectively. Results showed that AhR expression levels in breast cancer tissues were significantly higher than that in the non-cancer tissues. AhR expression was associated with the pathological type and P53 status, but not patients age, tumor grade and TNM, as well as ER, PR, C-erbB2, Ki-67, AR, EGFR status. Moreover, Western blot data suggested a negative correlation between p53 protein and AhR protein expression levels. The results suggest that high levels of AhR were expressed in the majority of breast cancer tissues and closely associated with P53 status and histological types of breast cancer. AHR and its abnormal expression may play an important role in multiple stages of breast cancer progression.
引用
收藏
页码:7931 / 7937
页数:7
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