Evidence map›Paper›PMID 27673563›Full record

ArticleMolecular therapy. Nucleic acids2016

Ecdysone Receptor-based Singular Gene Switches for Regulated Transgene Expression in Cells and Adult Rodent Tissues.

Seoghyun Lee, Kyung-Cheol Sohn, Dae-Kyoung Choi, Minho Won, Kyeong Ah Park, Sung-Kyu Ju, Kidong Kang, Young-Ki Bae, Gang Min Hur, Hyunju Ro

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2016. 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
0.3field-weighted citation impact, top 31% 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, 12 citations in OpenAlex.

  1. Disruption of constitutive CXCR4 oligomers impairs oncogenic properties in lymphoid neoplasms.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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

10 authors at 2 institutions in 1 country.

Seoghyun LeeDepartment of Biological Sciences, College of Bioscience and Biotechnology, Chungnam National University, Daejeon, Republic of Korea.
Kyung-Cheol SohnDepartment of Dermatology, College of Medicine, Chungnam National University, Daejeon, Republic of Korea.
Dae-Kyoung ChoiDepartment of Dermatology, College of Medicine, Chungnam National University, Daejeon, Republic of Korea.
Minho WonDepartment of Pharmacology, College of Medicine, Chungnam National University, Daejeon, Republic of Korea.
Kyeong Ah ParkDepartment of Pharmacology, College of Medicine, Chungnam National University, Daejeon, Republic of Korea.
Sung-Kyu JuAffiliated Research (and Development) Institute, Daejeon, Republic of Korea.
Kidong KangDepartment of Pharmacology, College of Medicine, Chungnam National University, Daejeon, Republic of Korea.
Young-Ki BaeComparative Biomedical Research Branch, Research Institute, National Cancer Center, Goyang, Republic of Korea.
Gang Min HurDepartment of Pharmacology, College of Medicine, Chungnam National University, Daejeon, Republic of Korea.
Hyunju RoDepartment of Biological Sciences, College of Bioscience and Biotechnology, Chungnam National University, Daejeon, Republic of Korea.
Chungnam National University · KRNational Cancer Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Controlled gene expression is an indispensable technique in biomedical research. Here, we report a convenient, straightforward, and reliable way to induce expression of a gene of interest with negligible background expression compared to the most widely used tetracycline (Tet)-regulated system. Exploiting a Drosophila ecdysone receptor (EcR)-based gene regulatory system, we generated nonviral and adenoviral singular vectors designated as pEUI(+) and pENTR-EUI, respectively, which contain all the required elements to guarantee regulated transgene expression (GAL4-miniVP16-EcR, termed GvEcR hereafter, and 10 tandem repeats of an upstream activation sequence promoter followed by a multiple cloning site). Through the transient and stable transfection of mammalian cell lines with reporter genes, we validated that tebufenozide, an ecdysone agonist, reversibly induced gene expression, in a dose- and time-dependent manner, with negligible background expression. In addition, we created an adenovirus derived from the pENTR-EUI vector that readily infected not only cultured cells but also rodent tissues and was sensitive to tebufenozide treatment for regulated transgene expression. These results suggest that EcR-based singular gene regulatory switches would be convenient tools for the induction of gene expression in cells and tissues in a tightly controlled fashion.

Identifiers

PMID27673563
PMCPMC5056996
OpenAlexW2526260291

What OpenQuestion holds

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Registered trials

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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.