Evidence map›Paper›PMID 33023539›Full record

ArticleBMC cancer2020

NFAT2 overexpression suppresses the malignancy of hepatocellular carcinoma through inducing Egr2 expression.

Jian Wang, Yamin Zhang, Lei Liu, Zilin Cui, Rui Shi, Jiancun Hou, Zirong Liu, Long Yang, Lianjiang Wang, Yang Li

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 31 citations in OpenAlex.

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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 1 institution in 1 country.

Jian WangHepatobiliary Surgery Department, Tianjin First Center Hospital, Tianjin Clinical Research Center for Organ Transplantation, Key Laboratory for Critical Care Medicine of the Ministry of Health, No. 24 Fukang Road, Nankai District, Tianjin, 300192, PR China.ORCID https://orcid.org/0000-0002-8411-8983
Yamin ZhangHepatobiliary Surgery Department, Tianjin First Center Hospital, Tianjin Clinical Research Center for Organ Transplantation, Key Laboratory for Critical Care Medicine of the Ministry of Health, No. 24 Fukang Road, Nankai District, Tianjin, 300192, PR China. 195156119@qq.com.ORCID http://orcid.org/0000-0002-9062-1788
Lei LiuDepartment of Transplantation Center, Tianjin First Center Hospital, Tianjin Clinical Research Center for Organ Transplantation, Key Laboratory for Critical Care Medicine of the Ministry of Health, Tianjin, 300192, PR China.
Zilin CuiHepatobiliary Surgery Department, Tianjin First Center Hospital, Tianjin Clinical Research Center for Organ Transplantation, Key Laboratory for Critical Care Medicine of the Ministry of Health, No. 24 Fukang Road, Nankai District, Tianjin, 300192, PR China.
Rui ShiHepatobiliary Surgery Department, Tianjin First Center Hospital, Tianjin Clinical Research Center for Organ Transplantation, Key Laboratory for Critical Care Medicine of the Ministry of Health, No. 24 Fukang Road, Nankai District, Tianjin, 300192, PR China.
Jiancun HouHepatobiliary Surgery Department, Tianjin First Center Hospital, Tianjin Clinical Research Center for Organ Transplantation, Key Laboratory for Critical Care Medicine of the Ministry of Health, No. 24 Fukang Road, Nankai District, Tianjin, 300192, PR China.
Zirong LiuHepatobiliary Surgery Department, Tianjin First Center Hospital, Tianjin Clinical Research Center for Organ Transplantation, Key Laboratory for Critical Care Medicine of the Ministry of Health, No. 24 Fukang Road, Nankai District, Tianjin, 300192, PR China.
Long YangHepatobiliary Surgery Department, Tianjin First Center Hospital, Tianjin Clinical Research Center for Organ Transplantation, Key Laboratory for Critical Care Medicine of the Ministry of Health, No. 24 Fukang Road, Nankai District, Tianjin, 300192, PR China.
Lianjiang WangHepatobiliary Surgery Department, Tianjin First Center Hospital, Tianjin Clinical Research Center for Organ Transplantation, Key Laboratory for Critical Care Medicine of the Ministry of Health, No. 24 Fukang Road, Nankai District, Tianjin, 300192, PR China.
Yang LiHepatobiliary Surgery Department, Tianjin First Center Hospital, Tianjin Clinical Research Center for Organ Transplantation, Key Laboratory for Critical Care Medicine of the Ministry of Health, No. 24 Fukang Road, Nankai District, Tianjin, 300192, PR China.
Tianjin First Center Hospital · CN

Funding

Tianjin Clinical Research Center for Organ Transplantation Project 15ZXLCSY00070
6 · The paper itself

Abstract

backgroundNuclear factor of activated T cells 2 (NFAT2) has been reported to regulate the development and malignancy of few tumors. In this study, we aimed to explore the effect of NFAT2 expression on cell fate of HepG2 cell and its potential mechanisms.

methodsFirstly, the pcDNA3.1-NFAT2 plasmid was transfected into HepG2 cells to construct NFAT2 overexpressed HepG2 cells. Then, the chemical count kit-8 cell viability assay, Annexin V-FITC apoptosis detection, EdU labeling proliferation detection, transwell and wound healing experiments were performed. The expression of Egr2 and FasL, and the phosphorylation of AKT and ERK, after ionomycin and PMA co-stimulation, was detected, while the Ca

resultsThe NFAT2 overexpression suppressed the cell viability, invasion and migration capabilities, and promoted apoptosis of HepG2 cells. NFAT2 overexpression induced the expression of Egr2 and FasL and suppressed the phosphorylation of AKT and ERK. The sensitivity and Ca

conclusionThe current study firstly suggested that NFAT2 suppressed the aggression and malignancy of HepG2 cells through inducing the expression of Egr2. The absence of NFAT2 and Egr2 in carcinoma tissues reminded us that NFAT2 may be a promising therapeutic target for hepatocellular carcinoma treatment.

Indexed as

ApoptosisCalciumCarcinoma, HepatocellularCell MovementCell SurvivalEarly Growth Response Protein 2Fas Ligand ProteinHep G2 CellsHumansLiver NeoplasmsNFATC Transcription FactorsPhosphorylationProto-Oncogene Proteins c-aktTransfectionUp-RegulationCalciumEarly Growth Response Protein 2EGR2 protein, humanFASLG protein, humanFas Ligand ProteinNFATC1 protein, humanNFATC Transcription FactorsProto-Oncogene Proteins c-aktCancer malignancyHepatocellular carcinomaHepG2 cellsNFAT2

Identifiers

PMID33023539
PMCPMC7542386
OpenAlexW3092585885

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.