Evidence map›Paper›PMID 20542918›Full record

ArticleNucleic acids research2010

Knocking down gene function with an RNA aptamer expressed as part of an intron.

Shengchun Wang, Xiaoching Zhao, Robert Suran, Volker M Vogt, John T Lis, Hua Shi

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. HSF1 as a Cancer Biomarker and Therapeutic Target.Current cancer drug targets · 2019
    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

6 authors at 2 institutions in 1 country.

Shengchun WangDepartment of Biological Sciences, University at Albany, State University of New York, Albany, NY 12222, USA.
Xiaoching Zhao
Robert Suran
Volker M Vogt
John T Lis
Hua Shi
Albany State University · USCornell University · US

Funding

Use of aptamers in dissecting the HSF-regulated cancer-enabling networkR01CA140730 · NCI · CORNELL UNIVERSITY · PI LIS, JOHN T, SHI, HUA · 2009 to 2012
$1.3M
NCI NIH HHS CA140730NCI NIH HHS R01 CA140730NIGMS NIH HHS GM40918
6 · The paper itself

Abstract

We developed a powerful expression system to produce aptamers and other types of functional RNA in yeast to examine their effects. Utilizing the intron homing process, the aptamer-coding sequences were integrated into hundreds of rRNA genes, and the aptamers were transcribed at high levels by RNA polymerase I without any additional promoter being introduced into the cell. We used this system to express an aptamer against the heat shock factor 1 (HSF1), a conserved transcription factor responsible for mobilizing specific genomic expression programs in response to stressful conditions such as elevated temperature. We observed a temperature sensitive growth retardation phenotype and specific decrease of heat shock gene expression. As HSF1 enables and promotes malignant growth and metastasis in mammals, and this aptamer binds yeast HSF1 and its mammalian ortholog with equal affinity, the results presented here attest to the potential of this aptamer as a specific and effective inhibitor of HSF1 activity.

Indexed as

Gene Expression RegulationIntronsAptamers, NucleotideDNA-Binding ProteinsGene Knockdown TechniquesHeat Shock Transcription FactorsPhenotypeRNASaccharomyces cerevisiaeTranscription FactorsAptamers, NucleotideDNA-Binding ProteinsHeat Shock Transcription FactorsRNATranscription Factors

Identifiers

PMID20542918
PMCPMC2926621
OpenAlexW2112588022

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.