Evidence map›Paper›PMID 36966163›Full record

ArticleCell death & disease2023

ZNF582 overexpression restrains the progression of clear cell renal cell carcinoma by enhancing the binding of TJP2 and ERK2 and inhibiting ERK2 phosphorylation.

Wuping Yang, Zedan Zhang, Lei Li, Kenan Zhang, Yawei Xu, Mancheng Xia, Jingcheng Zhou, Yanqing Gong, Jinchao Chen, Kan Gong

Open access · goldFull text read
In one paragraph

Article in Cell death & disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% 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, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
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  5. Article
  6. Review
  7. Article
  8. Promising predictive molecular biomarkers for cervical cancer (Review).International journal of molecular medicine · 2024
    Review
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  10. [Differential expression of NEDD8 in different pathological types of chronic rhinosinusitis with nasal polyps].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2023
    Article
  11. Article
  12. Biomarkers in renal cell carcinoma and their targeted therapies: a review.Exploration of targeted anti-tumor therapy · 2023
    Review
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 2 institutions in 1 country.

Wuping Yang *Department of Urology, Peking University First Hospital, Beijing, 100034, P.R. China.
Zedan Zhang *Department of Urology, Peking University First Hospital, Beijing, 100034, P.R. China.
Lei Li *Department of Urology, Peking University First Hospital, Beijing, 100034, P.R. China.
Kenan ZhangDepartment of Urology, Peking University First Hospital, Beijing, 100034, P.R. China.
Yawei XuDepartment of Urology, Peking University First Hospital, Beijing, 100034, P.R. China.
Mancheng XiaDepartment of Urology, Peking University First Hospital, Beijing, 100034, P.R. China.
Jingcheng ZhouDepartment of Urology, Peking University First Hospital, Beijing, 100034, P.R. China.ORCID 0000-0002-6226-5667
Yanqing GongDepartment of Urology, Peking University First Hospital, Beijing, 100034, P.R. China. yqgong@bjmu.edu.cn.
Jinchao ChenDepartment of Urologic Surgery, The Cancer Hospital of the University of Chinese Academy of Sciences, Zhejiang Cancer Hospital, Institute of Basic Medicine and Cancer (IBMC), Chinese Academy of Sciences, Hangzhou, 310022, P.R. China. runner421@126.com.
Kan GongDepartment of Urology, Peking University First Hospital, Beijing, 100034, P.R. China. gongkan_pku@126.com.ORCID 0000-0001-7195-677X
Peking University · CNZhejiang Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent evidences have suggested that Zinc finger protein 582 (ZNF582) plays different important roles in various tumors, but its clinical role, biological function and regulatory mechanism in clear cell renal cell carcinoma (ccRCC) are still vague. Through analyzing GEO and TCGA-KIRC data and validation with local samples, we identified the low expression pattern of ZNF582 in ccRCC. Decreased ZNF582 expression is correlated with higher tumor stage and grade, distant metastasis and poor prognosis. By analyzing the DNA methylation data of ccRCC in TCGA-KIRC and using Massarray DNA methylation and demethylation analysis, we confirmed the hypermethylation status of ZNF582 in ccRCC and its negative regulation on ZNF582 expression. Using cell phenotype experiments and orthotopic kidney tumor growth models, we determined the inhibitory effect of ZNF582 overexpression on ccRCC growth and metastasis in vivo and in vitro. Mechanistically, using TMT (Tandem mass tags) quantitative proteomics test, Co-IP (Co-immunoprecipitation) and Western Blot experiments, we clarified that ZNF582 binds to TJP2 and up-regulates TJP2 protein expression. Increased TJP2 protein combines with ERK2 to promote ERK2 protein expression and suppresses the phosphorylation of ERK2, thereby inhibiting the growth and metastasis of ccRCC. In general, our findings provide the first solid theoretical rationale for targeting ZNF582/TJP2/ERK2 axis to improve ccRCC treatment.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsCell Line, TumorGene Expression Regulation, NeoplasticHumansKidneyKruppel-Like Transcription FactorsPhosphorylationProteinsZonula Occludens-2 ProteinKruppel-Like Transcription FactorsProteinsTJP2 protein, humanZNF582 protein, humanZonula Occludens-2 Protein

Identifiers

PMID36966163
PMCPMC10039855
OpenAlexW4360938735

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read33
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.