Evidence map›Paper›PMID 26379276›Full record

ArticlePloS one2015

Novel miRNA-31 and miRNA-200a-Mediated Regulation of Retinoblastoma Proliferation.

Vanessa Montoya, Hanli Fan, Paul J Bryar, Joanna L Weinstein, Marilyn B Mets, Gang Feng, Joshua Martin, Alissa Martin, Hongmei Jiang, Nikia A Laurie

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. MicroRNAs as Regulators of Cancer Cell Energy Metabolism.Journal of personalized medicine · 2022
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Role of microRNA-25 in high glucose cultured Müller glia.International journal of ophthalmology · 2021
    Article
  11. Article
  12. Biomarkers in retinoblastoma.International journal of ophthalmology · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. Expression profiles and prognostic value of miRNAs in retinoblastoma.Journal of cancer research and clinical oncology · 2019
    Review
  17. Review
  18. Non-Coding RNAs in Retinoblastoma.Frontiers in genetics · 2019
    Review
  19. Article
  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

10 authors at 2 institutions in 1 country.

Vanessa MontoyaHuman Molecular Genetics Program, Lurie Children's Research Center, Chicago, Illinois, 60611, United States of America; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois, 60611, United States of America.
Hanli FanHuman Molecular Genetics Program, Lurie Children's Research Center, Chicago, Illinois, 60611, United States of America.
Paul J BryarDepartment of Ophthalmology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, 60611, United States of America; Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, 60611, United States of America.
Joanna L WeinsteinDepartment of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois, 60611, United States of America; Division of Hematology, Oncology, and Stem Cell Transplantation, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, 60611, United States of America.
Marilyn B MetsDepartment of Ophthalmology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, 60611, United States of America; Division of Ophthalmology, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, 60611, United States of America.
Gang FengClinical & Translational Sciences Institute, Northwestern University Feinberg School of Medicine, Chicago, Illinois, 60611, United States of America.
Joshua MartinHuman Molecular Genetics Program, Lurie Children's Research Center, Chicago, Illinois, 60611, United States of America.
Alissa MartinDivision of Hematology, Oncology, and Stem Cell Transplantation, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, 60611, United States of America.
Hongmei JiangDepartment of Statistics, Weinberg College of Arts & Sciences, Northwestern University, Evanston, Illinois, 60208, United States of America.
Nikia A LaurieHuman Molecular Genetics Program, Lurie Children's Research Center, Chicago, Illinois, 60611, United States of America; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois, 60611, United States of America; Division of Hematology, Oncology, and Stem Cell Transplantation, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, 60611, United States of America.
Northwestern University · USLurie Children's Hospital · US

Funding

Mentoring For Success: Developing Fundamental Skills For Biomedical ResearchR25GM079300 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MCGEE, RICHARD · 2007 to 2020
$6.6M
Elucidating the Role of MiR-31 in Retinoblastoma InvasionR21CA167225 · NCI · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI LAURIE, NIKIA ANITA · 2013 to 2014
$361k
NCI NIH HHS R21 CA167225NIGMS NIH HHS R25 GM079300
6 · The paper itself

Abstract

Retinoblastoma is the most common intraocular tumor in children. Current management includes broad-based treatments such as chemotherapy, enucleation, laser therapy, or cryotherapy. However, therapies that target specific pathways important for retinoblastoma progression could provide valuable alternatives for treatment. MicroRNAs are short, noncoding RNA transcripts that can regulate the expression of target genes, and their aberrant expression often facilitates disease. The identification of post-transcriptional events that occur after the initiating genetic lesions could further define the rapidly aggressive growth displayed by retinoblastoma tumors. In this study, we used two phenotypically different retinoblastoma cell lines to elucidate the roles of miRNA-31 and miRNA-200a in tumor proliferation. Our approach confirmed that miRNAs-31 and -200a expression is significantly reduced in human retinoblastomas. Moreover, overexpression of these two miRNAs restricts the expansion of a highly proliferative cell line (Y79), but does not restrict the growth rate of a less aggressive cell line (Weri1). Gene expression profiling of miRNA-31 and/or miRNA-200a-overexpressing cells identified differentially expressed mRNAs associated with the divergent response of the two cell lines. This work has the potential to enhance the development of targeted therapeutic approaches for retinoblastoma and improve the efficacy of treatment.

Indexed as

Cell Line, TumorCell ProliferationGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMicroRNAsRetinal NeoplasmsRetinoblastomaMicroRNAs

Identifiers

PMID26379276
PMCPMC4574557
OpenAlexW2172524080

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.