MicroRNA expression analysis and Multiplex ligation‐dependent probe amplification in metastatic and non‐metastatic uveal melanoma. (24th December 2013)

• Record Type: Journal Article
• Authors: Larsen, Ann‐Cathrine; Holst, Line; Kaczkowski, Bogumil; Andersen, Morten T.; Manfé, Valentina; Siersma, Volkert D.; Kolko, Miriam; Kiilgaard, Jens F.; Winther, Ole; Prause, Jan U.; Gniadecki, Robert; Heegaard, Steffen
• Is Part Of: Acta ophthalmologica. Volume 92:Number 6(2014)
• Page Start: 541
• Page End: 549
• Publication Date: 2013-12-24
• Subjects: Ophthalmology -- Periodicals; 617.7005
• DOI: 10.1111/aos.12322
• Languages: English
• ISSNs: 1755-375X

Abstract

<abstract abstract-type="main" id="aos12322-abs-0001"> <title>Abstract</title> <sec id="aos12322-sec-0001" sec-type="section"> <title>Purpose</title> <p>To determine the association of microRNA expression and chromosomal changes with metastasis and survival in uveal melanoma (UM).</p> </sec> <sec id="aos12322-sec-0002" sec-type="section"> <title>Methods</title> <p>Thirty‐six patients with UM were selected based on the metastatic status, and clinicopathological data were collected. Multiplex ligation‐dependent probe amplification (MLPA) was used to identify chromosomal changes. Chromosomal changes and clinicopathological data were correlated with survival and metastasis. The microRNA expression was analysed in 26 of the 36 archived UM samples. Unsupervised analysis, differential expression analysis and Cox regression analysis were performed to determine the association with metastasis and survival.</p> </sec> <sec id="aos12322-sec-0003" sec-type="section"> <title>Results</title> <p>Metastasis and metastatic death occurred in 20 patients, two patients died of other causes and one patient of unknown causes. A significant association between increasing size category (p = 0.002, log‐rank), extraocular extension (p = 0.001), chromosome 3 loss (p = 0.033) and 1p loss (p = 0.030) and development of metastases was observed. Tumour, node, metastasis (TNM) staging showed a significant association with survival (p < 0.0001, log‐rank). Adjusting for gender and age TNM size category T4 (p = 0.016, Cox regression analysis), mixed (p = 0.029) and epithelioid (p = 0.0058) cell types, chromosome 3 loss (p = 0.014) and 8q gain (p = 0.010) were significant prognosticators for a poor survival.</p> <p>Hierarchical clustering divided the UM into three groups based on microRNA expression. The clusters showed no association with clinical or histopathological features, TNM staging, metastasis or survival. Differential expression analysis did not reveal microRNAs related to metastasis or survival.</p> </sec> <sec id="aos12322-sec-0004" sec-type="section"> <title>Conclusions</title> <p>The prognostic significance of chromosome 3 loss and 8q gain identified by MLPA analysis was confirmed in archived UM samples. The value of microRNA expression as a predictor of metastasis and survival in UM could not be confirmed.</p> </sec> </abstract>