Evidence map›Paper›PMID 32133742›Full record

ArticleCancer science2020

Targeting USP1-dependent KDM4A protein stability as a potential prostate cancer therapy.

Shu-Zhong Cui, Zi-Ying Lei, Tian-Pei Guan, Ling-Ling Fan, You-Qiang Li, Xin-Yan Geng, De-Xue Fu, Hao-Wu Jiang, Song-Hui Xu

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Cancer science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Roles of USP1 in Ewing sarcoma.Genes & cancer · 2024
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. The crosstalk between ubiquitination and endocrine therapy.Journal of molecular medicine (Berlin, Germany) · 2023
    Review
  11. Analysis of Protein Degradation in Ferroptosis.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Hypoxia Enhances HIF1Stem cells international · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Shu-Zhong CuiDepartment of Abdominal Surgery, Affiliated Cancer Hospital and Institute of Guangzhou Medical University, Guangzhou, China.
Zi-Ying LeiDepartment of Abdominal Surgery, Affiliated Cancer Hospital and Institute of Guangzhou Medical University, Guangzhou, China.
Tian-Pei GuanDepartment of Abdominal Surgery, Affiliated Cancer Hospital and Institute of Guangzhou Medical University, Guangzhou, China.
Ling-Ling FanDepartment of Biochemistry, Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD, USA.
You-Qiang LiDepartment of Biochemistry, Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD, USA.
Xin-Yan GengDepartment of Biochemistry, Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD, USA.
De-Xue FuDepartment of Surgery, Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD, USA.
Hao-Wu JiangDepartment of Anesthesiology, Center for the Study of Itch, Washington University School of Medicine, St. Louis, MO, USA.
Song-Hui XuDepartment of Abdominal Surgery, Affiliated Cancer Hospital and Institute of Guangzhou Medical University, Guangzhou, China.ORCID https://orcid.org/0000-0003-0269-9129
University of Maryland, Baltimore · USGuangzhou Medical University · CNWashington University in St. Louis · US

Funding

Guangzhou Science High-Level Clinical Key Specialty Construction and Postdoctoral Science Foundation of China 2019M652852National Natural Science Foundation of China Grant No. 81972918
6 · The paper itself

Abstract

The histone demethylase lysine-specific demethylase 4A (KDM4A) is reported to be overexpressed and plays a vital in multiple cancers through controlling gene expression by epigenetic regulation of H3K9 or H3K36 methylation marks. However, the biological role and mechanism of KDM4A in prostate cancer (PC) remain unclear. Herein, we reported KDM4A expression was upregulation in phosphatase and tensin homolog knockout mouse prostate tissue. Depletion of KDM4A in PC cells inhibited their proliferation and survival in vivo and vitro. Further studies reveal that USP1 is a deubiquitinase that regulates KDM4A K48-linked deubiquitin and stability. Interestingly, we found c-Myc was a key downstream effector of the USP1-KDM4A/androgen receptor axis in driving PC cell proliferation. Notably, upregulation of KDM4A expression with high USP1 expression was observed in most prostate tumors and inhibition of USP1 promotes PC cells response to therapeutic agent enzalutamide. Our studies propose USP1 could be an anticancer therapeutic target in PC.

Indexed as

AnimalsAntineoplastic AgentsBenzamidesCell Line, TumorCell ProliferationCell SurvivalEnzyme InhibitorsGene ExpressionGene Expression Regulation, NeoplasticHEK293 CellsHumansJumonji Domain-Containing Histone DemethylasesMaleMiceMice, Mutant StrainsNitrilesAntineoplastic AgentsAR protein, humanBenzamidesenzalutamideEnzyme InhibitorsJumonji Domain-Containing Histone DemethylasesKDM4A protein, humanMYC protein, humanNitrilesPhenylthiohydantoinProto-Oncogene Proteins c-mycPTEN PhosphohydrolasePten protein, mouseReceptors, AndrogenUbiquitin-Specific ProteasesUSP1 protein, humandeubiquitinationKDM4Aprostate cancertumorigenesisUSP1

Identifiers

PMID32133742
PMCPMC7226285
OpenAlexW3009974692

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.