Evidence map›Paper›PMID 17961624›Full record

ArticleVirology2008

Transcriptional profiling of Vero E6 cells over-expressing SARS-CoV S2 subunit: insights on viral regulation of apoptosis and proliferation.

Yin-Shan Yeung, Chi-Wai Yip, Chung-Chau Hon, Ken Y C Chow, Iris C M Ma, Fanya Zeng, Frederick C C Leung

Open access · greenAbstract read
In one paragraph

Article in Virology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

21 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  8. Article
  9. Why do SARS-CoV-2 NSPs rush to the ER?Journal of neurology · 2021
    Review
  10. Genetic comparison among various coronavirus strains for the identification of potential vaccine targets of SARS-CoV2.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2021
    Review
  11. Article
  12. SARS-CoV-2 may regulate cellular responses through depletion of specific host miRNAs.American journal of physiology. Lung cellular and molecular physiology · 2020
    Article
  13. A hypothesized role for dysregulated bradykinin signaling in COVID-19 respiratory complications.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  14. 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

7 authors at 2 institutions in 1 country.

Yin-Shan YeungDepartment of Zoology, Kadoorie Biological Science Building, The University of Hong Kong, Hong Kong. ysyeung@graduate.hku.hk
Chi-Wai Yip
Chung-Chau Hon
Ken Y C Chow
Iris C M Ma
Fanya Zeng
Frederick C C Leung
University of Hong Kong · HKHKU-Pasteur Research Pole · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have previously demonstrated that over-expression of spike protein (S) of severe acute respiratory syndrome coronavirus (SARS-CoV) or its C-terminal subunit (S2) is sufficient to induce apoptosis in vitro. To further investigate the possible roles of S2 in SARS-CoV-induced apoptosis and pathogenesis of SARS, we characterized the host expression profiles induced upon S2 over-expression in Vero E6 cells by oligonucleotide microarray analysis. Possible activation of mitochondrial apoptotic pathway in S2 expressing cells was suggested, as evidenced by the up-regulation of cytochrome c and down-regulation of the Bcl-2 family anti-apoptotic members. Inhibition of Bcl-2-related anti-apoptotic pathway was further supported by the diminution of S2-induced apoptosis in Vero E6 cells over-expressing Bcl-xL. In addition, modulation of CCN E2 and CDKN 1A implied the possible control of cell cycle arrest at G1/S phase. This study is expected to extend our understanding on the pathogenesis of SARS at a molecular level.

Indexed as

ApoptosisCell ProliferationGene Expression ProfilingAnimalsCell LineCell SurvivalChlorocebus aethiopsGene Expression Regulation, ViralMembrane GlycoproteinsOligonucleotide Array Sequence AnalysisProtein SubunitsSevere Acute Respiratory SyndromeSpike Glycoprotein, CoronavirusTranscription, GeneticTransduction, GeneticVero CellsMembrane GlycoproteinsProtein SubunitsSpike Glycoprotein, CoronavirusViral Envelope Proteins

Identifiers

PMID17961624
PMCPMC7103328
OpenAlexW1966945132

What OpenQuestion holds

Textmetadata
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.