Evidence map›Paper›PMID 30550571›Full record

ArticlePloS one2018

microRNA-2110 functions as an onco-suppressor in neuroblastoma by directly targeting Tsukushi.

Zhenze Zhao, Veronica Partridge, Michaela Sousares, Spencer D Shelton, Cory L Holland, Alexander Pertsemlidis, Liqin Du

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. [miR-2110 Affects the Biological Behaviors of Lung Adenocarcinoma by Regulating CDT1].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. A review on Tsukushi: mammalian development, disorders, and therapy.Journal of cell communication and signaling · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
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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.

Zhenze ZhaoDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, Texas, United States of America.
Veronica PartridgeDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, Texas, United States of America.
Michaela SousaresDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, Texas, United States of America.
Spencer D SheltonDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, Texas, United States of America.
Cory L HollandDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, Texas, United States of America.
Alexander PertsemlidisGreehey Children's Cancer Research Institute, UT Health San Antonio, San Antonio, Texas, United States of America.
Liqin DuDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, Texas, United States of America.ORCID 0000-0002-7097-5861
Texas State University · USThe University of Texas Health Science Center at San Antonio · US

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
microRNA regulation of drug sensitivity in non-small cell lung cancerR01CA129632 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI PERTSEMLIDIS, ALEXANDER · 2007 to 2011
$1.6M
NCI NIH HHS P30 CA054174NCI NIH HHS R01 CA129632
6 · The paper itself

Abstract

microRNA-2110 (miR-2110) was previously identified as inducing neurite outgrowth in a neuroblastoma cell lines BE(2)-C, suggesting its differentiation-inducing and oncosuppressive function in neuroblastoma. In this study, we demonstrated that synthetic miR-2110 mimic had a generic effect on reducing cell survival in neuroblastoma cell lines with distinct genetic backgrounds, although the induction of cell differentiation traits varied between cell lines. In investigating the mechanisms underlying such functions of miR-2110, we identified that among its predicted target genes down-regulated by miR-2110, knockdown of Tsukushi (TSKU) expression showed the most potent effect in inducing cell differentiation and reducing cell survival, suggesting that TSKU protein plays a key role in mediating the functions of miR-2110. In investigating the clinical relevance of miR-2110 and TSKU expression in neuroblastoma patients, we found that low tumor miR-2110 levels were significantly correlated with high tumor TSKU mRNA levels, and that both low miR-2110 and high TSKU mRNA levels were significantly correlated with poor patient survival. These findings altogether support the oncosuppressive function of miR-2110 and suggest an important role for miR-2110 and its target TSKU in neuroblastoma tumorigenesis and in determining patient prognosis.

Indexed as

Biomarkers, TumorCarcinogenesisCell DifferentiationCell Line, TumorCell ProliferationCell SurvivalChildChild, PreschoolFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansIntercellular Signaling Peptides and ProteinsMaleMicroRNAsNeuroblastomaBiomarkers, TumorIntercellular Signaling Peptides and ProteinsMicroRNAsMIRN2110 microRNA, humanProteoglycansRNA, MessengerTSKU protein, human

Identifiers

PMID30550571
PMCPMC6294380
OpenAlexW2905329311

What OpenQuestion holds

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LicenceCC BY
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.