The role of microRNA deregulation in the pathogenesis of adrenocortical carcinoma

被引:158
作者
Ozata, Deniz M. [1 ,3 ]
Caramuta, Stefano [1 ,3 ]
Velazquez-Fernandez, David [1 ,3 ]
Akcakaya, Pinar [1 ,3 ]
Xie, Hong [1 ,3 ]
Hoog, Anders [2 ]
Zedenius, Jan [3 ,4 ]
Backdahl, Martin [3 ,4 ]
Larsson, Catharina [1 ,3 ]
Lui, Weng-Onn [1 ,3 ]
机构
[1] Karolinska Univ Hosp Solna, Ctr Mol Med, SE-17176 Stockholm, Sweden
[2] Karolinska Univ Hosp Solna, Dept Oncol Pathol, SE-17176 Stockholm, Sweden
[3] Karolinska Inst, Dept Mol Med & Surg, SE-17176 Stockholm, Sweden
[4] Karolinska Univ Hosp, Dept Breast & Endocrine Surg, SE-17176 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
HUMAN BREAST-CANCER; GENE-EXPRESSION; SUPPRESSES TUMORIGENICITY; MOLECULAR CLASSIFICATION; MICROARRAY ANALYSIS; COLORECTAL-CANCER; TUMORS; HYPOXIA; MALIGNANCY; CELLS;
D O I
10.1530/ERC-11-0082
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adrenocortical carcinoma (ACC) is an aggressive tumor showing frequent metastatic spread and poor survival. Although recent genome-wide studies of ACC have contributed to our understanding of the disease, major challenges remain for both diagnostic and prognostic assessments. The aim of this study was to identify specific microRNAs (miRNAs) associated with malignancy and survival of ACC patients. miRNA expression profiles were determined in a series of ACC, adenoma, and normal cortices using microarray. A subset of miRNAs showed distinct expression patterns in the ACC compared with adrenal cortices and adenomas. Among others, miR-483-3p, miR-483-5p, miR-210, and miR-21 were found overexpressed, while miR-195, miR-497, and miR-1974 were underexpressed in ACC. Inhibition of miR-483-3p or miR-483-5p and overexpression of miR-195 or miR-497 reduced cell proliferation in human NCI-H295R ACC cells. In addition, downregulation of miR-483-3p, but not miR-483-5p, and increased expression of miR-195 or miR-497 led to significant induction of cell death. Protein expression of p53 upregulated modulator of apoptosis (PUMA), a potential target of miR-483-3p, was significantly decreased in ACC, and inversely correlated with miR-483-3p expression. In addition, high expression of miR-503, miR-1202, and miR-1275 were found significantly associated with shorter overall survival among patients with ACC(Pvalues: 0.006, 0.005, and 0.042 respectively). In summary, we identified additional miRNAs associated with ACC, elucidated the functional role of four miRNAs in the pathogenesis of ACC cells, demonstrated the potential involvement of the pro-apoptotic factor PUMA (a miR-483-3p target) in adrenocortical tumors, and found novel miRNAs associated with survival in ACC. Endocrine-Related Cancer (2011) 18 643-655
引用
收藏
页码:643 / 655
页数:13
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