Evidence map›Paper›PMID 27453764›Full record

ArticleClinical epigenetics2016

Association of tumor and plasma microRNA expression with tumor monosomy-3 in patients with uveal melanoma.

Pierre L Triozzi, Susan Achberger, Wayne Aldrich, John W Crabb, Yogen Saunthararajah, Arun D Singh

Open access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 45 citations in OpenAlex.

  1. Role of miRNA in adult ocular tumorigenesis.Frontiers in molecular biosciences · 2025
    Review
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  5. Article
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  7. Article
  8. Spheroid-induced heterogeneity and plasticity of uveal melanoma cells.Cellular oncology (Dordrecht, Netherlands) · 2022
    Article
  9. Review
  10. Article
  11. Article
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  14. Emerging roles of microRNAs and their implications in uveal melanoma.Cellular and molecular life sciences : CMLS · 2021
    Review
  15. Review
  16. Review
  17. Article
  18. Observational
  19. Article
  20. A Review of MicroRNA in Uveal Melanoma.OncoTargets and therapy · 2020
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Pierre L TriozziTaussig Cancer Institute, Cleveland Clinic Foundation, Cleveland, OH USA ; Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157 USA.
Susan AchbergerTaussig Cancer Institute, Cleveland Clinic Foundation, Cleveland, OH USA.
Wayne AldrichTaussig Cancer Institute, Cleveland Clinic Foundation, Cleveland, OH USA.
John W CrabbCole Eye Institute, Cleveland Clinic Foundation, Cleveland, OH USA.
Yogen SaunthararajahTaussig Cancer Institute, Cleveland Clinic Foundation, Cleveland, OH USA.
Arun D SinghCole Eye Institute, Cleveland Clinic Foundation, Cleveland, OH USA.
Cleveland Clinic · USCleveland Eye Clinic · US

Funding

Uveal Melanoma MicrometastasisR01CA136776 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI TRIOZZI, PIERRE L · 2009 to 2010
$652k
NCI NIH HHS R01 CA136776NCI NIH HHS R01CA136776
6 · The paper itself

Abstract

backgroundEpigenetic events mediated by methylation and histone modifications have been associated with the development of metastasis in patients with uveal melanoma. The role of epigenetic events mediated by microRNA (miR) is less clear. Tumor and plasma miR expression was examined in patients with primary uveal melanoma with tumor monosomy-3, a predictor of metastasis.

resultsmiR profiling of tumors by microarray found six miRs over-expressed and 19 under-expressed in 33 tumors with monosomy-3 compared to 22 without. None of the miRs differentially expressed in tumors with and without monosomy-3 was differentially expressed in tumors with and without tumor infiltrating lymphocytes. Tumors manifesting monosomy-3 were also characterized by higher levels of TARBP2 and DDX17 and by lower levels of XPO5 and HIWI, miR biogenesis factors. miR profiling of plasma by a quantitative nuclease protection assay found elevated levels of 11 miRs and reduction in four in patients with tumor monosomy-3. Only three miRs differentially expressed in the tumor arrays were detectable in plasma. miRs implicated in uveal melanoma development were not differentially expressed. Elevated plasma levels in patients with tumor monosomy-3 of miR-92b, identified in the tumor array, and of miR-199-5p and miR-223, identified in the plasma array, were confirmed by quantitative real-time polymerase chain reaction. Levels were also higher in patients compared to normal controls.

conclusionsThese results support a role for epigenetic mechanisms in the development of metastasis in patients with uveal melanoma and the analysis of miRs as biomarkers of metastatic risk. They also suggest that potentially useful blood miRs may be derived from the host response as well as the tumor.

Indexed as

MonosomyChromosomes, Human, Pair 3Epigenesis, GeneticFemaleGene Expression Regulation, NeoplasticHumansMaleMelanomaMicroRNAsOligonucleotide Array Sequence AnalysisUveal MelanomaUveal NeoplasmsMicroRNAsMIR223, humanmirn199 microRNA, humanMIRN92 microRNA, humanBiomarkersmiR-199-5pmiR-223miR-92bPrognosis

Identifiers

PMID27453764
PMCPMC4957327
OpenAlexW2495352863

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.