Evidence map›Paper›PMID 30143009›Full record

ArticleCell communication and signaling : CCS2018

Wilms' tumor 1-associating protein plays an aggressive role in diffuse large B-cell lymphoma and forms a complex with BCL6 via Hsp90.

Yue Kuai, Xin Gong, Liya Ding, Fang Li, Lizhen Lei, Yuqi Gong, Qingmeng Liu, Huajiao Tan, Xinxia Zhang, Dongyu Liu and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. WTAP-induced mCell biochemistry and biophysics · 2025
    Article
  3. Article
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  5. WTAP Accelerates Exhaustion of CD8Mediators of inflammation · 2025
    Article
  6. NMolecular medicine (Cambridge, Mass.) · 2024
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. RNA m6A methylation regulators in liver cancer.Cancer cell international · 2024
    Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. The RNA mCell death & disease · 2022
    Review
  19. Review
  20. WTAP-mediated mCell death and differentiation · 2022
    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

16 authors at 6 institutions in 2 countries.

Yue KuaiDepartment of Pathology and Pathophysiology, Institute of Pathology and Forensic Medicine, Zhejiang University School of Medicine, Hangzhou, China.
Xin GongDepartment of Pathology and Pathophysiology, Institute of Pathology and Forensic Medicine, Zhejiang University School of Medicine, Hangzhou, China.
Liya DingDepartment of Pathology and Pathophysiology, Institute of Pathology and Forensic Medicine, Zhejiang University School of Medicine, Hangzhou, China.
Fang LiDepartment of Pathology and Pathophysiology, Institute of Pathology and Forensic Medicine, Zhejiang University School of Medicine, Hangzhou, China.
Lizhen LeiDepartment of Pathology and Pathophysiology, Institute of Pathology and Forensic Medicine, Zhejiang University School of Medicine, Hangzhou, China.
Yuqi GongDepartment of Pathology and Pathophysiology, Institute of Pathology and Forensic Medicine, Zhejiang University School of Medicine, Hangzhou, China.
Qingmeng LiuDepartment of Pathology, the Second Hospital of Shaoxing, Shaoxing, China.
Huajiao TanDepartment of Pathology and Pathophysiology, Institute of Pathology and Forensic Medicine, Zhejiang University School of Medicine, Hangzhou, China.
Xinxia ZhangEpitomics (Hangzhou) Inc, Hangzhou, China.
Dongyu LiuDepartment of Orthopedics, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Guoping RenDepartment of Pathology, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Hongyang PanEpitomics (Hangzhou) Inc, Hangzhou, China.
Yaoyao ShiDepartment of Pathology, Sir Run Run Show Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Friederike Berberich-SiebeltInstitute of Pathology, University of Würzburg, 97080, Würzburg, Germany.
Zhengrong MaoDepartment of Pathology and Pathophysiology, Institute of Pathology and Forensic Medicine, Zhejiang University School of Medicine, Hangzhou, China. maozr@zju.edu.cn.
Ren ZhouDepartment of Pathology and Pathophysiology, Institute of Pathology and Forensic Medicine, Zhejiang University School of Medicine, Hangzhou, China. zhouren@zju.edu.cn.ORCID 0000-0002-0599-8100
Zhejiang University · CNSir Run Run Shaw Hospital · CNFirst Affiliated Hospital Zhejiang University · CNSecond Affiliated Hospital of Zhejiang University · CNShaoxing Second Hospital · CNUniversity of Würzburg · DE

Funding

Health and Family Planning Commission of Zhejiang Province No.2018KY362National Natural Science Foundation of China (CN) No.81071937Nature Science Foundation of Zhejiang Province Nos. Y17H160070
6 · The paper itself

Abstract

backgroundWilms' tumor 1-associating protein (WTAP) is a nuclear protein, which is ubiquitously expressed in many tissues. Furthermore, in various types of malignancies WTAP is overexpressed and plays a role as an oncogene. The function of WTAP in diffuse large B-cell lymphoma (DLBCL), however, remains unclear.

methodsImmunohistochemistry was applied to evaluate the levels of WTAP expression in DLBCL tissues and normal lymphoid tissues. Overexpression and knock-down of WTAP in DLBCL cell lines, verified on mRNA and protein level served to analyze cell proliferation and apoptosis in DLBCL cell lines by flow cytometry. Finally, co-immunoprecipitation (Co-IP), IP, and GST-pull down assessed the interaction of WTAP with Heat shock protein 90 (Hsp90) and B-cell lymphoma 6 (BCL6) as well as determined the extend of its ubiquitinylation.

resultsWTAP protein levels were consistently upregulated in DLBCL tissues. WTAP promoted DLBCL cell proliferation and improved the ability to confront apoptosis, while knockdown of WTAP in DLBCL cell lines allowed a significant higher apoptosis rate after treatment with Etoposide, an anti-tumor drug. The stable expression of WTAP was depended on Hsp90. In line, we demonstrated that WTAP could form a complex with BCL6 via Hsp90 in vivo and in vitro.

conclusionWTAP is highly expressed in DLBCL, promoting growth and anti-apoptosis in DLBCL cell lines. WTAP is a client protein of Hsp90 and can appear in a complex with BCL6 and Hsp90 in DLBCL. Down-regulation of WTAP could improve the chemotherapeutic treatments in DLBCL.

Indexed as

ApoptosisCell Cycle ProteinsCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHSP90 Heat-Shock ProteinsHumansLymphoma, Large B-Cell, DiffuseNuclear ProteinsProtein BindingProtein StabilityProto-Oncogene Proteins c-bcl-6RNA Splicing FactorsBCL6 protein, humanCell Cycle ProteinsHSP90 Heat-Shock ProteinsNuclear ProteinsProto-Oncogene Proteins c-bcl-6RNA Splicing FactorsWTAP protein, humanBCL6ComplexDLBCLHsp90WTAP

Identifiers

PMID30143009
PMCPMC6108153
OpenAlexW2888457450

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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.