Evidence map›Paper›PMID 29270775›Full record

ArticlePathology oncology research : POR2020

ROCK1-PredictedmicroRNAs Dysregulation Contributes to Tumor Progression in Ewing Sarcoma.

G M Roberto, L E A Delsin, G M Vieira, M O Silva, R G Hakime, N F Gava, E E Engel, C A Scrideli, L G Tone, María Sol Brassesco

Abstract read
PubMed Publisher
In one paragraph

Article in Pathology oncology research : POR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 31% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Insight into the Role of the miR-584 Family in Human Cancers.International journal of molecular sciences · 2024
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. miRNA signatures in childhood sarcomas and their clinical implications.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 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

10 authors at 1 institution in 1 country.

G M RobertoRegional Blood Center, Ribeirão Preto School of Medicine, University of São Paulo, São Paulo, Brazil.
L E A DelsinDepartment of Genetics, Ribeirão Preto School of Medicine, University of São Paulo, São Paulo, Brazil.
G M VieiraDepartment of Genetics, Ribeirão Preto School of Medicine, University of São Paulo, São Paulo, Brazil.
M O SilvaDepartment Cell Biology, Ribeirão Preto School of Medicine, University of São Paulo, São Paulo, Brazil.
R G HakimeDepartment of Biology, Faculty of Philosophy, Sciences and Letters at Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
N F GavaDepartment of Biomechanics, Medicine and Rehabilitation of the Locomotor System, Ribeirão Preto School of Medicine, University of São Paulo, São Paulo, Brazil.
E E EngelDepartment of Biomechanics, Medicine and Rehabilitation of the Locomotor System, Ribeirão Preto School of Medicine, University of São Paulo, São Paulo, Brazil.
C A ScrideliDepartment of Pediatrics, Ribeirão Preto School of Medicine, University of São Paulo, São Paulo, Brazil.
L G ToneDepartment of Pediatrics, Ribeirão Preto School of Medicine, University of São Paulo, São Paulo, Brazil.
María Sol BrassescoDepartment of Biomechanics, Medicine and Rehabilitation of the Locomotor System, Ribeirão Preto School of Medicine, University of São Paulo, São Paulo, Brazil. solbrassesco@usp.br.
Universidade de São Paulo · BR

Funding

FAPESP 2014/03877-3
6 · The paper itself

Abstract

Over the last decade, the rho-associated kinases and several metastasis-associated microRNAs have emerged as important contributors of tumor invasion. However, despite prominence, our understanding of their involvement in the metastatic potential of Ewing Sarcoma (EWS) is incomplete. The expression profiles of ROCK1 or ROCK2 and miR-124-3p, miR-138-5p, miR-139-5p, miR-335-5p and miR-584-5p (all of which were previously predicted or validated to regulate these kinases) were evaluated through qRT-PCR and associated with clinical parameters. In vitro assays to evaluate colony formation and invasion/migration capacieties were performed on SK-ES-1 cells transfected with pre-miR mimics. ROCK1 expression was significantly reduced in EWS tissues, though there was no association with pathological parameters. miR-124-3p, miR-139-5p and miR-335-3p were also found significantly downregulated and positively correlated with ROCK1. Stratification indicated an association between lower levels of miR-139-5p and miR-584-5p with disease progression (p < 0.05), while reduced expression of the former and miR-124-3p were associated with reduced survival. In vitro miR-139-5p overexpression yielded inconsistent results: while mir-139-5p restoration significantly reduced invasion, the clonogenic capacity of cells was increased. Our study demonstrated that down-regulation of miR-124-3p, miR-139-5p and miR-584-5p are associated with disease progression in EWS and may serve as a risk assessment biomarkers though, as seen for mir-139-5p, their specific role remain to be elucidated for considering tailoring treatment options.

Indexed as

AdolescentAdultBone NeoplasmsCell Line, TumorCell MovementChildChild, PreschoolDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMaleMicroRNAsNeoplasm Invasivenessrho-Associated KinasesSarcoma, EwingMicroRNAsMIRN124 microRNA, humanMIRN139 microRNA, humanMIRN584 microRNA, humanrho-Associated KinasesROCK1 protein, humanEwing sarcomaInvasionmicroRNAMotilityRock

Identifiers

PMID29270775
OpenAlexW2779686347

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.