Evidence map›Paper›PMID 29970884›Full record

ArticleCell death & disease2018

An antisense RNA capable of modulating the expression of the tumor suppressor microRNA-34a.

Jason T Serviss, Nathanael Andrews, Jimmy Van den Eynden, Felix Clemens Richter, Miranda Houtman, Mattias Vesterlund, Laura Schwarzmueller, Per Johnsson, Erik Larsson, Dan Grandér and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 29 citations in OpenAlex.

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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

11 authors at 4 institutions in 3 countries.

Jason T ServissDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, SE-17177, Sweden. jason.serviss@ki.se.ORCID 0000-0002-5778-7014
Nathanael AndrewsDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, SE-17177, Sweden.
Jimmy Van den EyndenDepartment of Medical Biochemistry and Cell Biology, Institute of Biomedicine, The Sahlgrenska Academy, University of Gothenburg, SE-405 30, Gothenburg, Sweden.
Felix Clemens RichterDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, SE-17177, Sweden.ORCID 0000-0002-3415-3449
Miranda HoutmanDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, SE-17177, Sweden.
Mattias VesterlundDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, SE-17177, Sweden.
Laura SchwarzmuellerDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, SE-17177, Sweden.
Per JohnssonLudwig Institute for Cancer Research, Stockholm, Sweden.
Erik LarssonDepartment of Medical Biochemistry and Cell Biology, Institute of Biomedicine, The Sahlgrenska Academy, University of Gothenburg, SE-405 30, Gothenburg, Sweden.
Dan GrandérDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, SE-17177, Sweden.
Katja Pokrovskaja TammDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, SE-17177, Sweden.ORCID 0000-0001-6359-1256
Karolinska Institutet · SEUniversity of Gothenburg · SEAmsterdam UMC Location University of Amsterdam · NLKarolinska University Hospital · SE

Funding

Barncancerfonden (Swedish Childhood Cancer Foundation) PR2015-0009Cancerfonden (Swedish Cancer Society) 150768Radiumhemmets Forskningsfonder (Cancer Research Foundations of Radiumhemmet) 144063Vetenskapsrådet (Swedish Research Council) 521-2012-2037
6 · The paper itself

Abstract

The microRNA-34a is a well-studied tumor suppressor microRNA (miRNA) and a direct downstream target of TP53 with roles in several pathways associated with oncogenesis, such as proliferation, cellular growth, and differentiation. Due to its broad tumor suppressive activity, it is not surprising that miR34a expression is altered in a wide variety of solid tumors and hematological malignancies. However, the mechanisms by which miR34a is regulated in these cancers is largely unknown. In this study, we find that a long noncoding RNA transcribed antisense to the miR34a host gene, is critical for miR34a expression and mediation of its cellular functions in multiple types of human cancer. We name this long noncoding RNA lncTAM34a, and characterize its ability to facilitate miR34a expression under different types of cellular stress in both TP53-deficient and wild-type settings.

Indexed as

Blotting, WesternCell CycleCell Line, TumorCell ProliferationChromatin ImmunoprecipitationComputational BiologyDNA DamageGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHumansMicroRNAsPromoter Regions, GeneticRNA, AntisenseTandem Mass SpectrometryMicroRNAsMIRN34 microRNA, humanRNA, Antisense

Identifiers

PMID29970884
PMCPMC6030072
OpenAlexW2783537648

What OpenQuestion holds

Textmetadata
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.