Evidence map›Paper›PMID 35136014›Full record

ArticleCell death & disease2022

Stat4 rs7574865 polymorphism promotes the occurrence and progression of hepatocellular carcinoma via the Stat4/CYP2E1/FGL2 pathway.

Caie Wang, Na Gao, Lukui Yang, Yuanyuan Guo, Yan Fang, Tong Wang, Chen Xu, Gui Fang Li, Jun Zhou, Yunfei Zhang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2022. 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
1.4field-weighted citation impact, top 18% 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, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Investigating the Link betweenInternational journal of molecular sciences · 2024
    Article
  6. Review
  7. STAT4 gene polymorphisms in human diseases.Frontiers in immunology · 2024
    Review
  8. Article
  9. Association of theGenes · 2023
    Article
  10. Review
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

12 authors at 2 institutions in 1 country.

Caie Wang *Institute of Clinical Pharmacology, School of Medicine, Zhengzhou University, Zhengzhou, Henan, China.
Na Gao *Institute of Clinical Pharmacology, School of Medicine, Zhengzhou University, Zhengzhou, Henan, China.
Lukui YangDepartment of Pharmacy, the First Affiliated Hospital of Henan University of Science and Technology, Clinical Medical College of Henan University of Science and Technology, Luoyang, Henan, China.
Yuanyuan GuoInstitute of Clinical Pharmacology, School of Medicine, Zhengzhou University, Zhengzhou, Henan, China.
Yan FangInstitute of Clinical Pharmacology, School of Medicine, Zhengzhou University, Zhengzhou, Henan, China.
Tong WangInstitute of Clinical Pharmacology, School of Medicine, Zhengzhou University, Zhengzhou, Henan, China.
Chen XuInstitute of Clinical Pharmacology, School of Medicine, Zhengzhou University, Zhengzhou, Henan, China.
Gui Fang LiDepartment of Pharmacy, the First Affiliated Hospital of Henan University of Science and Technology, Clinical Medical College of Henan University of Science and Technology, Luoyang, Henan, China.
Jun ZhouInstitute of Clinical Pharmacology, School of Medicine, Zhengzhou University, Zhengzhou, Henan, China.
Yunfei ZhangInstitute of Clinical Pharmacology, School of Medicine, Zhengzhou University, Zhengzhou, Henan, China.
Qiang WenInstitute of Clinical Pharmacology, School of Medicine, Zhengzhou University, Zhengzhou, Henan, China.
Hailing QiaoInstitute of Clinical Pharmacology, School of Medicine, Zhengzhou University, Zhengzhou, Henan, China. qiaohl@zzu.edu.cn.ORCID http://orcid.org/0000-0002-8533-344X
Zhengzhou University · CNFirst Affiliated Hospital of Henan University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although there are many studies on the relationship between genetic polymorphisms and the incidence of diseases, mechanisms are rarely known. We report the mechanism by which signal transducer and activator of transcription 4 (stat4) rs7574865 promotes the occurrence and progression of hepatocellular carcinoma (HCC). We found that the GG genotype at stat4 rs7574865 was a risk genotype, and STAT4 levels in serum and peritumoral tissue from HCC patients with the GG genotype were significantly higher than those found in TT or TG carriers. Furthermore, HCC patients with the GG genotype or elevated STAT4 levels had poor prognoses. In vitro experiments demonstrated that STAT4 silencing promoted apoptosis and inhibited the invasion and migration of HepG2 and L02 cells. Proteomic analysis of HCC peritumors identified 273 proteins related to STAT4, of which CYP2E1 activity and FGL2 content exhibited the highest positive correlation. The relationship between CYP2E1 and FGL2 was also confirmed in cyp2e1

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsSTAT4 Transcription FactorAnimalsCase-Control StudiesCytochrome P-450 CYP2E1FibrinogenGenetic Predisposition to DiseaseGenotypeHumansMicePolymorphism, Single NucleotideProteomicsCytochrome P-450 CYP2E1FGL2 protein, humanFibrinogenSTAT4 protein, humanStat4 protein, mouseSTAT4 Transcription Factor

Identifiers

PMID35136014
PMCPMC8826371
OpenAlexW4210942366

What OpenQuestion holds

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Registered trials

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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.