Evidence map›Paper›PMID 36477795›Full record

ArticleJournal of medical virology2023

SARS-CoV-2 infection activates CREB/CBP in cellular cyclic AMP-dependent pathways.

Qi Yang, Jielin Tang, Juan Cao, Fengjiang Liu, Muqing Fu, Bao Xue, Anqi Zhou, Sijie Chen, Junjun Liu, Yuan Zhou and 3 more

Open access · greenAbstract read
In one paragraph

Article in Journal of medical virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
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

13 authors at 4 institutions in 1 country.

Qi YangChen Xinwen Lab in Department of Basic Research, Guangzhou Laboratory, Guangzhou, China.
Jielin TangChen Xinwen Lab in Department of Basic Research, Guangzhou Laboratory, Guangzhou, China.
Juan CaoHepatitis Virus and Gene Therapy Lab, State Key Laboratory of Virology, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, China.
Fengjiang LiuChen Xinwen Lab in Department of Basic Research, Guangzhou Laboratory, Guangzhou, China.
Muqing FuCenter for Infection & Immunity, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
Bao XueChen Xinwen Lab in Department of Basic Research, Guangzhou Laboratory, Guangzhou, China.
Anqi ZhouGMU-GIBH Joint School of Life Sciences, Guangzhou Medical University, Guangzhou, China.
Sijie ChenGMU-GIBH Joint School of Life Sciences, Guangzhou Medical University, Guangzhou, China.
Junjun LiuChen Xinwen Lab in Department of Basic Research, Guangzhou Laboratory, Guangzhou, China.
Yuan ZhouChen Xinwen Lab in Department of Basic Research, Guangzhou Laboratory, Guangzhou, China.
Yongxia ShiGuangzhou Customs District Technology Center, Guangzhou, China.
Wei PengChen Xinwen Lab in Department of Basic Research, Guangzhou Laboratory, Guangzhou, China.
Xinwen ChenChen Xinwen Lab in Department of Basic Research, Guangzhou Laboratory, Guangzhou, China.ORCID 0000-0002-4052-8155
Chinese Academy of Sciences · CNGuangzhou Experimental Station · CNGuangzhou Medical University · CNGuangzhou Institutes of Biomedicine and Health · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused a global coronavirus disease 2019 (COVID-19) pandemic that has affected the lives of billions of individuals. However, the host-virus interactions still need further investigation to reveal the underling mechanism of SARS-CoV-2 pathogenesis. Here, transcriptomics analysis of SARS-CoV-2 infection highlighted possible correlation between host-associated signaling pathway and virus. In detail, cAMP-protein kinase (PKA) pathway has an essential role in SARS-CoV-2 infection, followed by the interaction between cyclic AMP response element binding protein (CREB) and CREB-binding protein (CBP) could be induced and leading to the enhancement of CREB/CBP transcriptional activity. The replication of Delta and Omicron BA.5 were inhibited by about 49.4% and 44.7% after knockdown of CREB and CBP with small interfering RNAs, respectively. Furthermore, a small organic molecule naphthol AS-E (nAS-E), which targets on the interaction between CREB and CBP, potently inhibited SARS-CoV-2 wild-type (WT) infection with comparable the half-maximal effective concentration (EC

Indexed as

COVID-19Cyclic AMP Response Element-Binding ProteinHost-Pathogen InteractionsCREB-Binding ProteinCyclic AMPCyclic AMP-Dependent Protein KinasesHumansSARS-CoV-2CREB-Binding ProteinCyclic AMPCyclic AMP-Dependent Protein KinasesCyclic AMP Response Element-Binding ProteincAMP-PKACREB/CBPnAS-ESARS-CoV-2

Identifiers

PMID36477795
PMCPMC9877775
OpenAlexW4310958183

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.