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
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
相关论文
共 26 条
[1]   2,3,7,8-Tetrachlorodibenzo-p-Dioxin Counteracts the p53 Response to a Genotoxicant by Upregulating Expression of the Metastasis Marker AGR2 in the Hepatocarcinoma Cell Line HepG2 [J].
Ambolet-Camoit, Ariane ;
Bui, Linh Chi ;
Pierre, Stephane ;
Chevallier, Aline ;
Marchand, Alexandre ;
Coumoul, Xavier ;
Garlatti, Michele ;
Andreau, Karine ;
Barouki, Robert ;
Aggerbeck, Martine .
TOXICOLOGICAL SCIENCES, 2010, 115 (02) :501-512
[2]   Aryl Hydrocarbon Receptor Regulates Cell Cycle Progression in Human Breast Cancer Cells via a Functional Interaction with Cyclin-Dependent Kinase 4 [J].
Barhoover, Melissa A. ;
Hall, Julie M. ;
Greenlee, William F. ;
Thomas, Russell S. .
MOLECULAR PHARMACOLOGY, 2010, 77 (02) :195-201
[3]   Estrogen receptor α and aryl hydrocarbon receptor independent growth inhibitory effects of aminoflavone in breast cancer cells [J].
Brinkman, Ashley M. ;
Wu, Jiacai ;
Ersland, Karen ;
Xu, Wei .
BMC CANCER, 2014, 14
[4]   Malignant Transformation of Mammary Epithelial Cells by Ectopic Overexpression of the Aryl Hydrocarbon Receptor [J].
Brooks, J. ;
Eltom, S. E. .
CURRENT CANCER DRUG TARGETS, 2011, 11 (05) :654-669
[5]   Inhibition of constitutive aryl hydrocarbon receptor (AhR) signaling attenuates androgen independent signaling and growth in (C4-2) prostate cancer cells [J].
Cindy Tran ;
Richmond, Oliver ;
Aaron, LaTayia ;
Powell, Joann B. .
BIOCHEMICAL PHARMACOLOGY, 2013, 85 (06) :753-762
[6]   Phosphatases reverse p53-mediated cell cycle checkpoints [J].
Donehower, Lawrence A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (20) :7172-7173
[7]  
Draper London, 2006, AAOHN J, V54, P445
[8]   The Aryl Hydrocarbon Receptor Functions as a Tumor Suppressor of Liver Carcinogenesis [J].
Fan, Yunxia ;
Boivin, Gregory P. ;
Knudsen, Erik S. ;
Nebert, Daniel W. ;
Xia, Ying ;
Puga, Alvaro .
CANCER RESEARCH, 2010, 70 (01) :212-220
[9]   Role of aryl hydrocarbon receptor in cancer [J].
Feng, Shaolong ;
Cao, Zhaohui ;
Wang, Xinming .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2013, 1836 (02) :197-210
[10]   The Ah receptor in stem cell cycling, regulation, and quiescence [J].
Gasiewicz, Thomas A. ;
Singh, Kameshwar P. ;
Bennett, J. Allen .
BONE MARROW NICHE, STEM CELLS, AND LEUKEMIA: IMPACT OF DRUGS, CHEMICALS, AND THE ENVIRONMENT, 2014, 1310 :44-50