Immunohistochemical determination of the miR-1290 target arylamine N-acetyltransferase 1 (NAT1) as a prognostic biomarker in breast cancer

被引:51
作者
Endo, Yumi [1 ]
Yamashita, Hiroko [3 ]
Takahashi, Satoru [2 ]
Sato, Shinya [2 ]
Yoshimoto, Nobuyasu [1 ]
Asano, Tomoko [1 ]
Hato, Yukari [1 ]
Dong, Yu [1 ]
Fujii, Yoshitaka [1 ]
Toyama, Tatsuya [1 ]
机构
[1] Nagoya City Univ, Grad Sch Med Sci, Dept Oncol Immunol & Surg, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[2] Nagoya City Univ, Grad Sch Med Sci, Dept Expt Pathol & Tumor Biol, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[3] Hokkaido Univ Hosp, Dept Breast & Endocrine Surg, Sapporo, Hokkaido 0608648, Japan
基金
日本学术振兴会;
关键词
Breast cancer; miR-1290; Arylamine N-acetyltransferase 1 (NAT1); ESTROGEN-RECEPTOR-ALPHA; ARYLAMINE N-ACETYLTRANSFERASES; METABOLIZING-ENZYMES; EXPRESSION; TAMOXIFEN;
D O I
10.1186/1471-2407-14-990
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: There are many molecular differences between estrogen receptor alpha (ER alpha)-positive and ER-negative breast cancers. Recent analyses have shown that the former can be divided into two subtypes, luminal A and luminal B. These differ in response to endocrine therapy and chemotherapy, and in prognosis. In a previous study, we found that microRNA (miR)-1290 that was significantly down-regulated in luminal A tumors and its potential target arylamine N-acetyltransferase 1 (NAT1). The aim of the present study was to determine whether NAT1 is a bona fide target of miR-1290, and to investigate the impact of NAT1 on breast cancer prognosis. Methods: Luciferase reporter assays were employed to validate NAT1 as a putative miR-1290 target gene. Expression of NAT1, ER alpha, progesterone receptor (PgR) and HER2 was analyzed in 394 breast cancer samples by immunohistochemistry. Results: NAT1 was confirmed to be a direct target of miR-1290. Levels of expression of NAT1 were positively correlated with those of ER alpha (P < 0.0001) and PgR (P < 0.0001), but negatively correlated with both tumor grade and size (P < 0.0001). Kaplan-Meier analysis showed that the presence of NAT1 was significantly associated with increased overall survival (OS) (P = 0.0416) in these patients. Similarly, significant associations of NAT1 with disease-free survival (DFS) (P = 0.0048) and OS (P = 0.0055) in those patients who received adjuvant endocrine therapy with tamoxifen (n = 176) were found. Moreover, NAT1 was also significantly associated with increased DFS (P = 0.0025) and OS (P = 0.0007) in the subset of lymph node-positive patients (n = 147). Univariate and multivariate analyses showed significant associations between levels of NAT1 and DFS (P = 0.0005 and 0.019, respectively). Conclusions: We report that miR-1290 directly targets the NAT1 3'-UTR and that NAT1 protein expression is correlated with improved OS of breast cancer patients. NAT1 is a possible prognostic biomarker for lymph node-positive breast cancer. Thus, miR-1290 and its target NAT1 are associated with important characteristics of breast cancer.
引用
收藏
页数:9
相关论文
共 29 条
[1]   Comprehensive proteomic analysis of breast cancer cell membranes reveals unique proteins with potential roles in clinical cancer [J].
Adam, PJ ;
Boyd, R ;
Tyson, KL ;
Fletcher, GC ;
Stamps, A ;
Hudson, L ;
Poyser, HR ;
Redpath, N ;
Griffiths, M ;
Steers, G ;
Harris, AL ;
Patel, S ;
Berry, J ;
Loader, JA ;
Townsend, RR ;
Daviet, L ;
Legrain, P ;
Parekh, R ;
Terrett, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) :6482-6489
[2]  
Allred DC, 1998, MODERN PATHOL, V11, P155
[3]  
Belian E, 2010, ANTICANCER RES, V30, P629
[4]   Relationship between intratumoral expression of genes coding for xenobiotic-metabolizing enzymes and benefit from adjuvant tamoxifen in estrogen receptor alpha-positive postmenopausal breast carcinoma [J].
Bièche, I ;
Girault, I ;
Urbain, E ;
Tozlu, S ;
Lidereau, R .
BREAST CANCER RESEARCH, 2004, 6 (03) :R252-R263
[5]   MicroRNA expression profiling of human breast cancer identifies new markers of tumor subtype [J].
Blenkiron, Cherie ;
Goldstein, Leonard D. ;
Thorne, Natalie P. ;
Spiteri, Inmaculada ;
Chin, Suet-Feung ;
Dunning, Mark J. ;
Barbosa-Morais, Nuno L. ;
Teschendorff, Andrew E. ;
Green, Andrew R. ;
Ellis, Ian O. ;
Tavare, Simon ;
Caldas, Carlos ;
Miska, Eric A. .
GENOME BIOLOGY, 2007, 8 (10)
[6]   Induction of human arylamine N-acetyltransferase type I by androgens in human prostate cancer cells [J].
Butcher, Neville J. ;
Tetlow, Natasha L. ;
Cheung, Catherine ;
Broadhurst, Gysell M. ;
Minchin, Rodney F. .
CANCER RESEARCH, 2007, 67 (01) :85-92
[7]   Arylamine N-Acetyltransferase 1: A Novel Drug Target in Cancer Development [J].
Butcher, Neville J. ;
Minchin, Rodney F. .
PHARMACOLOGICAL REVIEWS, 2012, 64 (01) :147-165
[8]   Classification of breast cancer using genetic algorithms and tissue microarrays [J].
Dolled-Filhart, Marisa ;
Ryden, Lisa ;
Cregger, Melissa ;
Jirstroem, Karin ;
Harigopal, Malini ;
Camp, Robert L. ;
Rimm, David L. .
CLINICAL CANCER RESEARCH, 2006, 12 (21) :6459-6468
[9]   miR-1290 and its potential targets are associated with characteristics of estrogen receptor α-positive breast cancer [J].
Endo, Yumi ;
Toyama, Tatsuya ;
Takahashi, Satoru ;
Yoshimoto, Nobuyasu ;
Iwasa, Mai ;
Asano, Tomoko ;
Fujii, Yoshitaka ;
Yamashita, Hiroko .
ENDOCRINE-RELATED CANCER, 2013, 20 (01) :91-102
[10]   Oncomirs - microRNAs with a role in cancer [J].
Esquela-Kerscher, A ;
Slack, FJ .
NATURE REVIEWS CANCER, 2006, 6 (04) :259-269