Evidence map›Paper›PMID 38031139›Full record

ArticleClinical epigenetics2023

EZH2 K63-polyubiquitination affecting migration in extranodal natural killer/T-cell lymphoma.

Boheng Li, Qidi Zhou, Qin Wan, Xuan Qiao, Shangying Chen, Jianbiao Zhou, Zhijun Wuxiao, Lei Luo, Siok-Bian Ng, Jieping Li and 1 more

Open access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. 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

11 authors at 5 institutions in 2 countries.

Boheng LiCollege of Pharmaceutical Sciences, Southwest University, Chongqing, China. liboheng1023@swu.edu.cn.
Qidi ZhouCollege of Pharmaceutical Sciences, Southwest University, Chongqing, China.
Qin WanCollege of Pharmaceutical Sciences, Southwest University, Chongqing, China.
Xuan QiaoCollege of Pharmaceutical Sciences, Southwest University, Chongqing, China.
Shangying ChenBioinformatics Core, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Jianbiao ZhouCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
Zhijun WuxiaoDepartment of Hematology, Lymphoma and Myeloma Center, The First Affiliated Hospital of Hainan Medical University, Haikou, China.
Lei LuoCollege of Pharmaceutical Sciences, Southwest University, Chongqing, China.
Siok-Bian NgCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
Jieping LiDepartment of Hematology Oncology, Chongqing University Cancer Hospital, Chongqing, China. 84000411qiqin@cqu.edu.cn.
Wee-Joo ChngCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore. mdccwj@nus.edu.sg.
Southwest University · CNNational University of Singapore · SGChongqing Cancer Hospital · CNHainan Medical University · CNNational University Cancer Institute, Singapore · SG

Funding

Central University Basic Research fund SWU021003National Natural Science foundation of China 82100208Natural Science foundation of Chongqing CSTB2022NSCQ-MSX0348
6 · The paper itself

Abstract

backgroundOverexpressed EZH2 is oncogenically involved in the pathogenesis of different cancerous contexts including extranodal natural killer/T cell lymphoma (ENKTL). However, the underlying mechanisms of EZH2 upregulation have not been fully clarified and it is still difficult to target EZH2 in ENKTL.

resultsCurrent study identifies an E3 ligase TRIP12 that triggers K63-linked polyubiquitination of EZH2 in ENKTL and unexpectedly, stabilizes EZH2. As determined by gene expression profiling (GEP), TRIP12 and EZH2 levels correlate with each other in ENKTL patient samples. Aided by quantitative mass spectrometry (MS) and follow-up analysis, we identify K634 as the ubiquitination site of EZH2. Further study confirms that TRIP12-mediated EZH2 K634 ubiquitination enhances the interaction between EZH2 and SUZ12 or CDK1 and increases the level of EZH2 T487 phosphorylation. This study further demonstrates the TRIP12-EZH2 signaling might be regulated by cytoplasmic HSP60. Importantly, the TRIP12-EZH2 axis mediates ENKTL cell migration via accelerating epithelial-mesenchymal transition (EMT). Moreover, our study finds out dexamethasone treatment manipulates TRIP12-EZH2 signaling and may represent a novel therapeutic strategy against ENKTL metastasis.

conclusionsAltogether, TRIP12 induces K63-linked site-specific polyubiquitination of EZH2 for stabilization, which promotes ENKTL cell migration and could be targeted by dexamethasone treatment.

Indexed as

Lymphoma, Extranodal NK-T-CellCarrier ProteinsDexamethasoneDNA MethylationEnhancer of Zeste Homolog 2 ProteinHumansKiller Cells, NaturalUbiquitinationUbiquitin-Protein LigasesCarrier ProteinsDexamethasoneEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanTRIP12 protein, humanUbiquitin-Protein LigasesExtranodal natural killer/T-cell lymphomaEZH2K63-polyubiquitinationMigrationTRIP12

Identifiers

PMID38031139
PMCPMC10685657
OpenAlexW4389149258

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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.