Long noncoding RNA profiles of adrenocortical cancer can be used to predict recurrence

被引:54
作者
Glover, A. R. [1 ]
Zhao, J. T. [1 ]
Ip, J. C. [1 ]
Lee, J. C. [1 ]
Robinson, B. G. [1 ,2 ]
Gill, A. J. [1 ,3 ,4 ]
Soon, P. S. H. [5 ,6 ,7 ]
Sidhu, S. B. [1 ,8 ]
机构
[1] Royal N Shore Hosp, Canc Genet Lab, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
[2] Royal N Shore Hosp, Dept Endocrinol, St Leonards, NSW 2065, Australia
[3] Royal N Shore Hosp, Dept Anat Pathol, St Leonards, NSW 2065, Australia
[4] Univ Sydney, St Leonards, NSW 2065, Australia
[5] Bankstown Hosp, Dept Surg, Bankstown, NSW 2065, Australia
[6] Univ New S Wales, Bankstown, NSW 2065, Australia
[7] Ingham Inst Appl Med Res, Liverpool, NSW 2200, Australia
[8] Univ Sydney, Royal N Shore Hosp, Endocrine Surg Unit, St Leonards, NSW 2065, Australia
关键词
long noncoding RNA; PRINS; epigenetics; recurrence; metastasis; microarray; adrenocortical; GENE-EXPRESSION; TUMOR-SUPPRESSOR; BETA-CATENIN; CARCINOMA; FEATURES; CELLS; IGF; CLASSIFICATION; METHYLATION; PROGRESSION;
D O I
10.1530/ERC-14-0457
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adrenocortical carcinoma (ACC) is an aggressive malignancy with high rates of recurrence following surgical resection. Long noncoding RNAs (lncRNAs) play an important role in cancer development. Pathogenesis of adrenal tumours have been characterised by mRNA, microRNA and methylation expression signatures, but it is unknown if this extends to lncRNAs. This study describes lncRNA expression signatures in ACC, adrenal cortical adenoma (ACA) and normal adrenal cortex (NAC) and presents lncRNAs associated with ACC recurrence to identify novel prognostic and therapeutic targets. RNA was extracted from freshly frozen tissue with confirmation of diagnosis by histopathology. Focused lncRNA and mRNA transcriptome analysis was performed using the ArrayStar Human LncRNA V3.0 microarray. Differentially expressed lncRNAs were validated using quantitative reverse transcriptase-PCR and correlated with clinical outcomes. Microarray of 21 samples (ten ACCs, five ACAs and six NACs) showed distinct patterns of lncRNA expression between each group. A total of 956 lncRNAs were differentially expressed between ACC and NAC, including known carcinogenesis-related lncRNAs such as H19, GAS5, MALAT1 and PRINS (P <= 0.05); 85 lncRNAs were differentially expressed between ACC and ACA (P <= 0.05). Hierarchical clustering and heat mapping showed ACC samples correctly grouped compared with NAC and ACA. Sixty-six differentially expressed lncRNAs were found to be associated with ACC recurrence (P <= 0.05), one of which, PRINS, was validated in a group of 20 ACCs and also found to be associated with metastatic disease on presentation. The pathogenesis of adrenal tumours extends to lncRNA dysregulation and low expression of the lncRNA PRINS is associated with ACC recurrence.
引用
收藏
页码:99 / 109
页数:11
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