Endo Yumi, Yamashita Hiroko, Takahashi Satoru, Sato Shinya, Yoshimoto Nobuyasu, Asano Tomoko, Hato Yukari, Dong Yu, Fujii Yoshitaka, Toyama Tatsuya
Department of Oncology, Immunology and Surgery, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan.
BMC Cancer. 2014 Dec 20;14:990. doi: 10.1186/1471-2407-14-990.
There are many molecular differences between estrogen receptor α (ERα)-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.
Luciferase reporter assays were employed to validate NAT1 as a putative miR-1290 target gene. Expression of NAT1, ERα, progesterone receptor (PgR) and HER2 was analyzed in 394 breast cancer samples by immunohistochemistry.
NAT1 was confirmed to be a direct target of miR-1290. Levels of expression of NAT1 were positively correlated with those of ERα (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).
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.
雌激素受体α(ERα)阳性和ER阴性乳腺癌之间存在许多分子差异。最近的分析表明,前者可分为两种亚型,即管腔A型和管腔B型。这两种亚型在内分泌治疗和化疗反应以及预后方面存在差异。在先前的一项研究中,我们发现微小RNA(miR)-1290在管腔A型肿瘤中显著下调,及其潜在靶点芳胺N-乙酰基转移酶1(NAT1)。本研究的目的是确定NAT1是否是miR-1290的真正靶点,并研究NAT1对乳腺癌预后的影响。
采用荧光素酶报告基因检测法验证NAT1作为假定的miR-1290靶基因。通过免疫组织化学分析394例乳腺癌样本中NAT1、ERα、孕激素受体(PgR)和HER2的表达。
NAT1被证实是miR-1290的直接靶点。NAT1的表达水平与ERα(P<0.0001)和PgR(P<0.0001)的表达水平呈正相关,但与肿瘤分级和大小均呈负相关(P<0.0001)。Kaplan-Meier分析显示,NAT1的存在与这些患者的总生存期(OS)显著增加相关(P = 0.0416)。同样,在接受他莫昔芬辅助内分泌治疗的患者(n = 176)中,发现NAT1与无病生存期(DFS)(P = 0.0048)和OS(P = 0.0055)有显著关联。此外,在淋巴结阳性患者亚组(n = 147)中,NAT1也与DFS(P = 0.0025)和OS(P = 0.0007)的增加显著相关。单因素和多因素分析显示NAT1水平与DFS之间存在显著关联(分别为P = 0.0005和0.019)。
我们报告miR-1290直接靶向NAT1的3'-UTR,且NAT1蛋白表达与乳腺癌患者OS改善相关。NAT1是淋巴结阳性乳腺癌的一种可能的预后生物标志物。因此,miR-1290及其靶点NAT1与乳腺癌的重要特征相关。