Evidence map›Paper›PMID 30407747›Full record

ArticleMolecular genetics & genomic medicine2018

Functional variants of the ATG7 gene promoter in acute myocardial infarction.

Pei Zhang, Jie Zhang, Yexin Zhang, Shuai Wang, Shuchao Pang, Bo Yan

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. LncRNAiScience · 2026
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  4. Protein homeostasis in the aged and diseased heart.The journal of cardiovascular aging · 2023
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  5. Review
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  8. Moments in autophagy and disease: Past and present.Molecular aspects of medicine · 2021
    Review
  9. Article
  10. Review
  11. 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

6 authors at 3 institutions in 1 country.

Pei ZhangCollege of Clinical Medicine, Xinxiang Medical University, Xinxiang, Henan, China.
Jie ZhangDepartment of Medicine, Shandong University School of Medicine, Jinan, Shandong, China.
Yexin ZhangDepartment of Medicine, Shandong University School of Medicine, Jinan, Shandong, China.
Shuai WangDepartment of Medicine, Shandong University School of Medicine, Jinan, Shandong, China.
Shuchao PangShandong Provincial Key Laboratory of Cardiac Disease Diagnosis and Treatment, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, Shandong, China.
Bo YanShandong Provincial Key Laboratory of Cardiac Disease Diagnosis and Treatment, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, Shandong, China.ORCID 0000-0003-1391-5683
Shandong University · CNAffiliated Hospital of Jining Medical University · CNJining First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronary artery disease including acute myocardial infarction (AMI) is mainly caused by atherosclerosis, an inflammatory and metabolic disease. Autophagy has been demonstrated to play critical roles in lipid metabolism and inflammation. Altered autophagic activity has been reported in AMI patients. However, molecular basis for dysfunctional autophagy in AMI remains unexplained.

methodsIn this study, the promoter of the ATG7 gene, encoding a core protein for autophagy, was genetically and functionally analyzed in large cohorts of AMI patients (n = 355) and ethnic-matched healthy controls (n = 363). Related molecular mechanisms were also explored.

resultsA total of 19 DNA sequence variants (DSVs) including single-nucleotide polymorphisms (SNPs) were found in the ATG7 gene promoter. Two novel DSVs and five SNPs were only identified in AMI patients group. These DSVs and SNPs, except one SNP, significantly altered the transcriptional activity of the ATG7 gene promoter in both HEK-293 and H9c2 cells (p < 0.05). Further electrophoretic mobility shift assay revealed that the DSVs and SNPs evidently affected the binding of transcription factors.

conclusionsATG7 gene DSVs and SNPs identified in AMI patients may alter the transcriptional activity of the ATG7 gene promoter and change ATG7 level, contributing to the AMI development as a rare risk factor.

Indexed as

Polymorphism, Single NucleotideAutophagy-Related Protein 7FemaleHEK293 CellsHumansMaleMiddle AgedMyocardial InfarctionPromoter Regions, GeneticATG7 protein, humanAutophagy-Related Protein 7acute myocardial infarctionATG7autophagyDNA sequence variantsgeneticspromoter

Identifiers

PMID30407747
PMCPMC6305654
OpenAlexW2899953656

What OpenQuestion holds

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LicenceCC BY
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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.