Evidence map›Paper›PMID 31088504›Full record

ArticleJournal of translational medicine2019

miRNA deregulation targets specific pathways in leiomyosarcoma development: an in silico analysis.

Clara Benna, Senthilkumar Rajendran, Marco Rastrelli, Simone Mocellin

Abstract read
In one paragraph

Article in Journal of translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Review
  2. Current research in parasitology & vector-borne diseases · 2025
    Article
  3. Review
  4. Review
  5. Placental miR-3940-3p Is Associated With Maternal Insulin Resistance in Late Pregnancy.The Journal of clinical endocrinology and metabolism · 2021
    Article
  6. Extracellular Vesicle-Contained microRNA ofFrontiers in cellular and infection microbiology · 2020
    Article
  7. Review
  8. Ion channels in sarcoma: pathophysiology and treatment options.Pflugers Archiv : European journal of physiology · 2019
    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

4 authors.

Clara BennaDepartment of Surgery Oncology and Gastroenterology, University of Padova, Padua, Italy. clara.benna@unipd.it.ORCID 0000-0002-9077-2471
Senthilkumar RajendranDepartment of Surgery Oncology and Gastroenterology, University of Padova, Padua, Italy.
Marco RastrelliSurgical Oncology Unit, Istituto Oncologico Veneto (IOV-IRCCS), Padua, Italy.
Simone MocellinDepartment of Surgery Oncology and Gastroenterology, University of Padova, Padua, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroRNA (miRNA) mediate post-transcriptional gene repression and are involved in a variety of human diseases, including cancer. Soft tissue sarcomas are rare malignancies with a variety of histological subtypes which may occur virtually anywhere in the human body. Leiomyosarcoma is one of the most common subtypes, shows a smooth muscle phenotype and its cancerogenesis is still unclear. The aim of our study was to investigate the potential role of miRNA differential expression in leiomyosarcoma development.

methodsWe first employed the Sarcoma microRNA Expression Database, a repository that describes the patterns of over 1000 miRNA expression in various human sarcoma types, to identify differentially expressed miRNA comparing leiomyosarcoma and smooth muscle samples. Subsequently, we identified putative target genes of those miRNAs with the TargetScan prediction tool. Finally, we evaluated whether the retrieved pool of putative targets was enriched in genes belonging to specific molecular pathways by means of the Enrichr analysis tool. Protein-protein network analysis was analyzed by means of the STRING web tool.

resultsOut of 1120 miRNAs tested, the expression of 301 miRNAs was statistically significantly different between leiomyosarcoma and smooth muscle samples. The hypothetical targets could be predicted for 172 miRNAs. 438 genes were predicted to be the targets with high confidence (cumulative weighted context score cut-off level less than - 1.0) and analyzed for belonging to specific molecular pathways. Pathway analysis suggested that RNA Polymerase III, tRNA functions and synaptic neurotransmission (with special regard to dopamine mediated signaling) could be involved in leiomyosarcoma development.

conclusionsOur results demonstrate that data mining of publicly available repositories can be useful to suggest molecular pathways underlying the pathogenesis of rare tumors such as leiomyosarcoma.

Indexed as

Computer SimulationGene Expression Regulation, NeoplasticGene Expression ProfilingGene Regulatory NetworksGenes, NeoplasmHumansLeiomyosarcomaMicroRNAsSignal TransductionMicroRNAsDopamineLeiomyosarcomamicroRNAmiRNAPathway analysisRNA pol IIIRNA polymerase IIISarcoma

Identifiers

PMID31088504
PMCPMC6515658

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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.