Evidence map›Paper›PMID 37288663›Full record

ArticleJCI insight2023

RNF112-mediated FOXM1 ubiquitination suppresses the proliferation and invasion of gastric cancer.

Shengwei Zhang, Jing Wang, Weichao Hu, Lijiao He, Qingyun Tang, Jie Li, Mengmeng Jie, Xinzhe Li, Cheng Liu, Qin Ouyang and 2 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
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

18 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  11. Structural and functional characterization of the brain-specific dynamin superfamily member RNF112.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. The transcription factor FOXQ1 in cancer.Cancer metastasis reviews · 2025
    Review
  13. Article
  14. Article
  15. 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

12 authors at 2 institutions in 1 country.

Shengwei ZhangDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Jing WangMedical Research Institute, Southwest University, Chongqing, China.
Weichao HuDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Lijiao HeDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Qingyun TangDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Jie LiDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Mengmeng JieDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Xinzhe LiDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Cheng LiuDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Qin OuyangDepartment of Pharmaceutical Chemistry, College of Pharmacy and Laboratory Medicine, Third Military Medical University, Chongqing, China.
Shiming YangDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Changjiang HuDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Army Medical University · CNSouthwest University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Forkhead box M1 (FOXM1) plays a critical role in development physiologically and tumorigenesis pathologically. However, insufficient efforts have been dedicated to exploring the regulation, in particular the degradation of FOXM1. Here, the ON-TARGETplus siRNA library targeting E3 ligases was used to screen potential candidates to repress FOXM1. Of note, mechanism study revealed that RNF112 directly ubiquitinates FOXM1 in gastric cancer, resulting in a decreased FOXM1 transcriptional network and suppressing the proliferation and invasion of gastric cancer. Interestingly, the well-established small-molecule compound RCM-1 significantly enhanced the interaction between RNF112 and FOXM1, which further promoted FOXM1 ubiquitination and subsequently exerted promising anticancer effects in vitro and in vivo. Altogether, we demonstrate that RNF112 suppresses gastric cancer progression by ubiquitinating FOXM1 and highlight the RNF112/FOXM1 axis serves as both prognosis biomarker and therapeutic target in gastric cancer.

Indexed as

DNA-Binding ProteinsForkhead Box Protein M1Stomach NeoplasmsCarcinogenesisCell ProliferationHumansUbiquitinationDNA-Binding ProteinsForkhead Box Protein M1FOXM1 protein, humanRING finger protein 112, humanCancer gene therapyGastric cancerGastroenterologyOncogenesOncology

Identifiers

PMID37288663
PMCPMC10259508
OpenAlexW4379744270

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.