Evidence map›Paper›PMID 23550645›Full record

ReviewImmunological reviews2013

mir-17-92: a polycistronic oncomir with pleiotropic functions.

Virginie Olive, Qijing Li, Lin He

Abstract readReview
In one paragraph

Review in Immunological reviews, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% 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

94 citing papers in PubMed, 1 synthesis or guideline pooled it, 151 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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  5. Review
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  7. Article
  8. Review
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  12. Article
  13. Review
  14. Review
  15. Article
  16. miRNA in Molecular Diagnostics.Bioengineering (Basel, Switzerland) · 2022
    Review
  17. Article
  18. Review
  19. Review
  20. Review

34 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Virginie OliveDivision of Cellular and Developmental Biology, MCB Department, University of California at Berkeley, Berkeley, CA 94705, USA.
Qijing Li
Lin He
University of California, Berkeley · USDuke University Hospital · US

Funding

miR-200 miRNAs repress tumor metastasis in lung adenocarcinomaR01CA139067 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI HE, LIN · 2009 to 2021
$3.3M
A new technology to isolate RNP complexes of a polycistronic miRNA oncogeneR21CA175560 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI HE, LIN · 2013 to 2014
$360k
NCI NIH HHS R01 CA139067NCI NIH HHS R21 CA175560
6 · The paper itself

Abstract

Neoplastic transformation is caused by accumulation of genetic lesions that ultimately convert normal cells into tumor cells with uncontrolled proliferation and survival, unlimited replicative potential, and invasive growth. Emerging evidence has highlighted the functional importance of non-coding RNAs, particularly microRNAs (miRNAs), in the initiation and progression of tumor development. The mir-17-92 miRNA is among the best characterized miRNA oncogenes, whose genomic amplification or aberrant elevation are frequently observed in a variety of tumor types. Unlike protein-coding oncogenes, where one transcript produces one protein, mir-17-92 encodes a polycistronic miRNA transcript that yields six individual miRNA components. This unique gene structure, shared by many important miRNA oncogenes and tumor suppressors, underlies the unique functionality of mir-17-92 in a cell type and context-dependent manner. Recent functional dissection of mir-17-92 indicates that individual mir-17-92 components perform distinct biological functions, which collectively regulate multiple related cellular processes during development and disease. The structural complexity of mir-17-92 as a polycistronic miRNA oncogene, along with the complex mode of interactions among its components, constitutes the molecular basis for its unique functional complexity during normal and tumor development.

Indexed as

Cell Transformation, NeoplasticAnimalsCellular MicroenvironmentGene Expression Regulation, NeoplasticHumansMicroRNAsNeoplasmsOncogenesOrgan SpecificityRNA, Long NoncodingStructure-Activity RelationshipMicroRNAsMIR17HG, humanRNA, Long Noncoding

Identifiers

PMID23550645
PMCPMC3972423
OpenAlexW1971615688

What OpenQuestion holds

Textmetadata
LicenceTDM
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.