Evidence map›Paper›PMID 22509080›Full record

ArticleWorld journal of gastroenterology2012

HBx activates FasL and mediates HepG2 cell apoptosis through MLK3-MKK7-JNKs signal module.

Ren-Xian Tang, Fan-Yun Kong, Bao-Feng Fan, Xiao-Mei Liu, Hong-Juan You, Peng Zhang, Kui-Yang Zheng

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

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  4. The Roles of c-Jun N-Terminal Kinase (JNK) in Infectious Diseases.International journal of molecular sciences · 2021
    Review
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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

7 authors at 1 institution in 1 country.

Ren-Xian TangDepartment of Pathogenic Biology and Lab of Infection and Immunology, Xuzhou Medical College, Xuzhou, Jiangsu Province, China.
Fan-Yun Kong
Bao-Feng Fan
Xiao-Mei Liu
Hong-Juan You
Peng Zhang
Kui-Yang Zheng
Xuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate the possible mechanism by which hepatitis B virus X protein (HBx) mediates apoptosis of HepG2 cells.

methodsHBx expression vector pcDNA3.1-X was transfected into HepG2 cells to establish an HBx high-expression cellular model as pcDNA3.1-X transfected group. The pcDNA3.1-X and pSilencer3.1-shHBX (HBx antagonist) were cotransfected into HepG2 cells to establish an HBx low-expression model as RNAi group. Untransfected HepG2 cells and HepG2 cells transfected with negative control plasmid were used as controls. Apoptosis rate, the expression of Fas/FasL signaling pathway-related proteins and the phosphorylation levels of MLK3, MKK7 and JNKs, which are upstream molecules of death receptor pathways and belong to the family of mitogen-activated protein kinases (MAPKs), were measured in each group.

resultsCompared with HepG2 cell group and RNAi group, apoptosis rate, the expression of Fas and FasL proteins, and the activation of MLK3, MKK7 and JNKs were increased in the pcDNA3.1-X transfected group. The activation of JNKs and expression of FasL protein were inhibited in the pcDNA3.1-X transfected group when treated with a known JNK inhibitor, SP600125. When authors treated pcDNA3.1-X transfected group with K252a, a known MLK3 inhibitor, the activation of MLK3, MKK7 and JNKs as well as expression of FasL protein was inhibited. Furthermore, cell apoptosis rate was also significantly declined in the presence of K252a in the pcDNA3.1-X transfected group.

conclusionHBx can induce HepG2 cell apoptosis via a novel active MLK3-MKK7-JNKs signaling module to upregulate FasL protein expression.

Indexed as

AnimalsApoptosisCaspasesEnzyme ActivationEnzyme InhibitorsFas Ligand Proteinfas ReceptorHep G2 CellsHumansJNK Mitogen-Activated Protein KinasesMAP Kinase Kinase 7MAP Kinase Kinase KinasesMAP Kinase Signaling SystemMitogen-Activated Protein Kinase Kinase Kinase 11Trans-ActivatorsViral Regulatory and Accessory ProteinsCaspasesEnzyme InhibitorsFas Ligand Proteinfas Receptorhepatitis B virus X proteinJNK Mitogen-Activated Protein KinasesMAP2K7 protein, humanMAP Kinase Kinase 7MAP Kinase Kinase KinasesMitogen-Activated Protein Kinase Kinase Kinase 11Trans-ActivatorsViral Regulatory and Accessory ProteinsApoptosisFasLHepatitis B virus X proteinHepG2 cellMLK3

Identifiers

PMID22509080
PMCPMC3319944
OpenAlexW2074275961

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.