Evidence map›Paper›PMID 33038763›Full record

ArticleEBioMedicine2020

Pan-cancer analysis of somatic mutations in miRNA genes.

Martyna O Urbanek-Trzeciak, Paulina Galka-Marciniak, Paulina M Nawrocka, Ewelina Kowal, Sylwia Szwec, Maciej Giefing, Piotr Kozlowski

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

39 citing papers in PubMed, 58 citations in OpenAlex.

  1. MicroRNAs as Biomarkers of Cervical Cancers.International journal of molecular sciences · 2026
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  9. microRNAs as Biomarkers of Breast Cancer.International journal of molecular sciences · 2025
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  19. miRNAs in pancreatic cancer progression and metastasis.Clinical & experimental metastasis · 2024
    Review
  20. Article
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

7 authors at 2 institutions in 1 country.

Martyna O Urbanek-TrzeciakInstitute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland.
Paulina Galka-MarciniakInstitute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland.
Paulina M NawrockaInstitute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland.
Ewelina KowalInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Sylwia SzwecInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Maciej GiefingInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Piotr KozlowskiInstitute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland. Electronic address: kozlowp@ibch.poznan.pl.
Institute of Bioorganic Chemistry, Polish Academy of Sciences · PLInstitute of Human Genetics · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundmiRNAs are considered important players in oncogenesis, serving either as oncomiRs or suppressormiRs. Although the accumulation of somatic alterations is an intrinsic aspect of cancer development and many important cancer-driving mutations have been identified in protein-coding genes, the area of functional somatic mutations in miRNA genes is heavily understudied.

methodsHere, based on the analysis of large genomic datasets, mostly the whole-exome sequencing of over 10,000 cancer/normal sample pairs deposited within the TCGA repository, we undertook an analysis of somatic mutations in miRNA genes.

findingsWe identified and characterized over 10,000 somatic mutations and showed that some of the miRNA genes are overmutated in Pan-Cancer and/or specific cancers. Nonrandom occurrence of the identified mutations was confirmed by a strong association of overmutated miRNA genes with KEGG pathways, most of which were related to specific cancer types or cancer-related processes. Additionally, we showed that mutations in some of the overmutated genes correlate with miRNA expression, cancer staging, and patient survival.

interpretationOur study is the first comprehensive Pan-Cancer study of cancer somatic mutations in miRNA genes. It may help to understand the consequences of mutations in miRNA genes and the identification of miRNA functional mutations. The results may also be the first step (form the basis and provide the resources) in the development of computational and/or statistical approaches/tools dedicated to the identification of cancer-driver miRNA genes.

fundingThis work was supported by research grants from the Polish National Science Centre 2016/22/A/NZ2/00184 and 2015/17/N/NZ3/03629.

Indexed as

Genetic Predisposition to DiseaseMutationBiomarkers, TumorCell Transformation, NeoplasticComputational BiologyDisease ProgressionExome SequencingGene Expression ProfilingGenetic Association StudiesGenomicsHumansMicroRNAsNeoplasmsPrognosisRNA PrecursorsSequence Analysis, RNABiomarkers, TumorMicroRNAsRNA PrecursorsmiRNANon-codingPan-CancerSomatic mutationsTCGA

Identifiers

PMID33038763
PMCPMC7648123
OpenAlexW3092539938

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LicenceCC BY-NC-ND
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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.