Evidence map›Paper›PMID 25892965›Full record

ArticleInternational journal of biological sciences2015

Recognition of cytosolic DNA attenuates glucose metabolism and induces AMPK mediated energy stress response.

Min Zheng, Linna Xie, Yaoji Liang, Suqin Wu, Huijuan Xu, Yuedong Zhang, Hekun Liu, Dexin Lin, Jiahuai Han, Kunping Lu

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Regulating STING in health and disease.Journal of inflammation (London, England) · 2017
    Review
  7. 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

10 authors at 1 institution in 1 country.

Min Zheng1. Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, Fujian, 350108, China. ; 2. Translational Medicine Institute, Fujian Medical University, Fuzhou, Fujian, 350108, China.
Linna Xie1. Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, Fujian, 350108, China. ; 3. Department of Bioengineering, Fujian Vocational College of Bioengineering, Fuzhou, Fujian, 350007, China.
Yaoji Liang4. State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, Fujian, 361102, China.
Suqin Wu4. State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, Fujian, 361102, China.
Huijuan Xu2. Translational Medicine Institute, Fujian Medical University, Fuzhou, Fujian, 350108, China.
Yuedong Zhang2. Translational Medicine Institute, Fujian Medical University, Fuzhou, Fujian, 350108, China.
Hekun Liu2. Translational Medicine Institute, Fujian Medical University, Fuzhou, Fujian, 350108, China.
Dexin Lin1. Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, Fujian, 350108, China.
Jiahuai Han4. State Key Laboratory of Cellular Stress Biology and School of Life Sciences, Xiamen University, Xiamen, Fujian, 361102, China.
Kunping Lu2. Translational Medicine Institute, Fujian Medical University, Fuzhou, Fujian, 350108, China. ; 5. Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Fujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Both viral infection and DNA transfection expose single-stranded or double-stranded DNA to the cytoplasm of mammalian cells. Recognition of cytosolic DNA activates a series of cellular responses, including induction of pro-inflammatory genes such as type I interferon through the well-known cGAS-STING pathway. Here we show for the first time that intracellular administration of either single or double stranded interferon stimulating DNA (ISD), but not poly(dA) suppresses cell growth in many different cell types. Suppression of cell growth by cytosolic DNA is cGAS/STING independent and associated with inhibition of glucose metabolism, ATP depletion and subsequent cellular energy stress responses including activation of AMPK and inactivation of mTORC1. Our results suggest that in concert with but independent of innate immune response, recognition of cytosolic DNA induced cellular energy stress potentially functions as a metabolic barrier to viral replication.

Indexed as

AMP-Activated Protein KinasesCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseCytosolDNAEnergy MetabolismGene Expression RegulationGlucoseHEK293 CellsHumansMechanistic Target of Rapamycin Complex 1Membrane ProteinsMultiprotein ComplexesNucleotidyltransferasesPoly ASTING ProteinStress, PhysiologicalAMP-Activated Protein KinasescGAS protein, humanCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseDNAGlucoseMechanistic Target of Rapamycin Complex 1Membrane ProteinsMultiprotein ComplexesNucleotidyltransferasesPoly Apoly(dA)STING1 protein, humanSTING ProteinTOR Serine-Threonine KinasesAMPKATP depletionCytosolic DNAEnergy stressGlycolysis

Identifiers

PMID25892965
PMCPMC4400389
OpenAlexW2103560510

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.