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MicroRNA profiling of benign and malignant pheochromocytomas identifies novel diagnostic and therapeutic targets.

Authors :
Meyer-Rochow GY
Jackson NE
Conaglen JV
Whittle DE
Kunnimalaiyaan M
Chen H
Westin G
Sandgren J
Stålberg P
Khanafshar E
Shibru D
Duh QY
Clark OH
Kebebew E
Gill AJ
Clifton-Bligh R
Robinson BG
Benn DE
Sidhu SB
Source :
Endocrine-related cancer [Endocr Relat Cancer] 2010 Aug 16; Vol. 17 (3), pp. 835-46. Date of Electronic Publication: 2010 Aug 16 (Print Publication: 2010).
Publication Year :
2010

Abstract

MicroRNAs (miRNAs) are small RNAs ( approximately 22 bp) that post-transcriptionally regulate protein expression and are found to be differentially expressed in a number of human cancers. There is increasing evidence to suggest that miRNAs could be useful in cancer diagnosis, prognosis, and therapy. We performed miRNA microarray expression profiling on a cohort of 12 benign and 12 malignant pheochromocytomas and identified a number of differentially expressed miRNAs. These results were validated in a separate cohort of ten benign and ten malignant samples using real-time quantitative RT-PCR; benign samples had a minimum follow-up of at least 2 years. It was found that IGF2 as well as its intronic miR-483-5p was over-expressed, while miR-15a and miR-16 were under-expressed in malignant tumours compared with benign tumours. These miRNAs were found to be diagnostic and prognostic markers for malignant pheochromocytoma. The functional role of miR-15a and miR-16 was investigated in vitro in the rat PC12 pheochromocytoma cell line, and these miRNAs were found to regulate cell proliferation via their effect on cyclin D1 and apoptosis. These data indicate that miRNAs play a pivotal role in the biology of malignant pheochromocytoma, and represent an important class of diagnostic and prognostic biomarkers and therapeutic targets warranting further investigation.

Details

Language :
English
ISSN :
1479-6821
Volume :
17
Issue :
3
Database :
MEDLINE
Journal :
Endocrine-related cancer
Publication Type :
Academic Journal
Accession number :
20621999
Full Text :
https://doi.org/10.1677/ERC-10-0142