Evidence map›Paper›PMID 33953708›Full record

ArticleFrontiers in immunology2021

Glycolytic Metabolism Is Critical for the Innate Antibacterial Defense in Acute

Fangmei Fan, Yurong Ma, Rongshuang Ai, Zhiqiang Ding, Dingyi Li, Yiting Zhu, Qian He, Xinxin Zhang, Yilin Dong, Yujuan He

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. IgM mediated cefotaxime resistance ofAmerican journal of translational research · 2025
    Article
  5. Review
  6. Article
  7. Article
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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.

Fangmei FanDepartment of Laboratory Medicine, Key Laboratory of Diagnostic Medicine (Ministry of Education), Chongqing Medical University, Chongqing, China.
Yurong MaDepartment of Laboratory Medicine, Key Laboratory of Diagnostic Medicine (Ministry of Education), Chongqing Medical University, Chongqing, China.
Rongshuang AiDepartment of Laboratory Medicine, Key Laboratory of Diagnostic Medicine (Ministry of Education), Chongqing Medical University, Chongqing, China.
Zhiqiang DingSchool of Computer Science, Chongqing Institute of Engineering, Chongqing, China.
Dingyi LiDepartment of Laboratory Medicine, Key Laboratory of Diagnostic Medicine (Ministry of Education), Chongqing Medical University, Chongqing, China.
Yiting ZhuDepartment of Laboratory Medicine, Key Laboratory of Diagnostic Medicine (Ministry of Education), Chongqing Medical University, Chongqing, China.
Qian HeDepartment of Laboratory Medicine, Key Laboratory of Diagnostic Medicine (Ministry of Education), Chongqing Medical University, Chongqing, China.
Xinxin ZhangDepartment of Laboratory Medicine, Key Laboratory of Diagnostic Medicine (Ministry of Education), Chongqing Medical University, Chongqing, China.
Yilin DongDepartment of Laboratory Medicine, Key Laboratory of Diagnostic Medicine (Ministry of Education), Chongqing Medical University, Chongqing, China.
Yujuan HeDepartment of Laboratory Medicine, Key Laboratory of Diagnostic Medicine (Ministry of Education), Chongqing Medical University, Chongqing, China.
Chongqing Medical University · CNKunming Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Methods: The levels of glycolytic metabolism were evaluated by measuring the expression of glycolysis-related genes and the production of metabolites. HE stain, immunofluorescence, immunohistochemistry, enzyme-linked immunosorbent assay (ELISA) and Western blot were performed to measure the effect of glucose metabolic reprogramming on inflammatory response, pneumococcal clearance, hypoxia-inducible factor 1 alpha (HIF-1α) expression and cytokine secretion during AOM, respectively. Results: The analysis of microarray revealed an increase of the expression of glycolysis-related genes during Conclusion:

Indexed as

GlycolysisAnimalsDisease Models, AnimalEar, MiddleGene Expression Regulation, EnzymologicHost-Pathogen InteractionsHypoxia-Inducible Factor 1, alpha SubunitInflammation MediatorsInterleukin-1betaMiceMice, Inbred C57BLNeutrophilsOtitis MediaPhagocytosisPneumococcal InfectionsStreptococcus pneumoniaeHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitIL1B protein, mouseInflammation MediatorsInterleukin-1betaTnf protein, mouseTumor Necrosis Factor-alphaglycolysishypoxia inducible factor-1αinnate immunityneutrophilsotitis media

Identifiers

PMID33953708
PMCPMC8089373
OpenAlexW3153495870

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.