Evidence map›Paper›PMID 33629943›Full record

ArticleOncology research2021

()-Epigallocatechin-3-Gallate Inhibits EBV Lytic Replication via Targeting LMP1-Mediated MAPK Signal Axes.

Hongde Li, Yueshuo Li, Jianmin Hu, Sufang Liu, Xiangjian Luo, Min Tang, Ann M Bode, Zigang Dong, Xinqi Liu, Weihua Liao and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Oncology research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Sumac Polyphenols as Pan-Herpesvirus Inhibitors.International journal of molecular sciences · 2025
    Article
  4. Review
  5. Review
  6. Review
  7. Article
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

11 authors at 5 institutions in 2 countries.

Hongde LiKey Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Department of Radiology, Xiangya Hospital, Central South UniversityChangshaP.R. China.
Yueshuo LiKey Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Department of Radiology, Xiangya Hospital, Central South UniversityChangshaP.R. China.
Jianmin HuKey Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Department of Radiology, Xiangya Hospital, Central South UniversityChangshaP.R. China.
Sufang LiuDivision of Hematology, Institute of Molecular Hematology, the Second Xiangya Hospital, Central South University at ChangshaChangshaP.R. China.
Xiangjian LuoKey Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Department of Radiology, Xiangya Hospital, Central South UniversityChangshaP.R. China.
Min TangKey Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Department of Radiology, Xiangya Hospital, Central South UniversityChangshaP.R. China.
Ann M BodeThe Hormel Institute, University of MinnesotaAustin, MNUSA.
Zigang DongThe Hormel Institute, University of MinnesotaAustin, MNUSA.
Xinqi LiuState Key Laboratory of Medicinal Chemical Biology, College of Life Sciences, Nankai University at TianjinTianjinP.R. China.
Weihua LiaoDepartment of Radiology, Xiangya Hospital, Central South University at ChangshaChangshaP.R. China.
Ya CaoKey Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Department of Radiology, Xiangya Hospital, Central South UniversityChangshaP.R. China.
Central South University · CNXiangya Hospital Central South University · CNHormel (United States) · USNankai University · CNUniversity of Minnesota · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

EpsteinBarr virus (EBV)-encoded latent membrane protein 1 (LMP1) plays an important oncogenic role in the viral latent infection. Recently, increasing evidence indicates that the high expression of LMP1 during EBV lytic cycle is related to the viral lytic replication. However, the mechanism by which LMP1 regulates EBV lytic replication remains unclear. ()-Epigallocatechin-3-gallate (EGCG) prevents carcinogenesis by directly targeting numerous membrane proteins and effectively inhibits EBV lytic cascade. Here, we demonstrated that LMP1 promotes EBV lytic replication through the downstream signal molecules MAPKs, including ERKs, p38, and JNKs. LMP1 induces the phosphorylation of p53 through MAPKs to enhance the ability of wild-type p53 (wt-p53) to activate expression of BZLF1 gene, while the JNKs/c-Jun signal axis appears to be involved in EBV lytic replication induced by LMP1 in p53 mutant manner. We provided the first evidence that EGCG directly targets the viral membrane LMP1 (

Indexed as

Antiviral AgentsCatechinCell Line, TumorEpstein-Barr Virus InfectionsHerpesvirus 4, HumanHumansMAP Kinase Signaling SystemMitogen-Activated Protein KinasesMutationPhosphorylationPromoter Regions, GeneticTumor Suppressor Protein p53Viral Matrix ProteinsVirus ReplicationAntiviral AgentsCatechinEBV-associated membrane antigen, Epstein-Barr virusepigallocatechin gallateMitogen-Activated Protein KinasesTumor Suppressor Protein p53Viral Matrix Proteins

Identifiers

PMID33629943
PMCPMC8420900
OpenAlexW3130817662

What OpenQuestion holds

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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.