Evidence map›Paper›PMID 32677374›Full record

ArticleCancer medicine2020

Tripartite motif containing 24 regulates cell proliferation in colorectal cancer through YAP signaling.

Wenlin Xie, Yingqiang Zhang, Bingyang Wang, Yuting Hu, Bohui Zhan, Fangqiang Wei, Jianming Tang, Jiayan Lian

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.0field-weighted citation impact, top 14% 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, 28 citations in OpenAlex.

  1. Review
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  10. Early onset Arboleda-Tham syndrome due toFrontiers in genetics · 2025
    Article
  11. Review
  12. Review
  13. Advances in the antitumor mechanisms of tripartite motif-containing protein 3.Journal of cancer research and clinical oncology · 2024
    Review
  14. Review
  15. Review
  16. Tctp, a unique Ing5-binding partner, inhibits the chromatin binding of Enok inProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. Article
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  20. 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

8 authors at 2 institutions in 1 country.

Wenlin XieDepartment of Pathology, The Seventh Affiliated Hospital of Sun Yat-Sen University, Shenzhen, Guangdong, P.R. China.
Yingqiang ZhangDepartment of Interventional Radiology, The Seventh Affiliated Hospital of Sun Yat-Sen University, Shenzhen, Guangdong, P.R. China.
Bingyang WangDepartment of Pathology, The Seventh Affiliated Hospital of Sun Yat-Sen University, Shenzhen, Guangdong, P.R. China.
Yuting HuDepartment of Pathology, The Seventh Affiliated Hospital of Sun Yat-Sen University, Shenzhen, Guangdong, P.R. China.
Bohui ZhanDepartment of Pathology, The Seventh Affiliated Hospital of Sun Yat-Sen University, Shenzhen, Guangdong, P.R. China.
Fangqiang WeiDepartment of Hepatobiliary and Pancreatic Surgery, Zhejiang Provincial People' s Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, Zhejiang, P.R. China.ORCID 0000-0003-0871-2275
Jianming TangDepartment of Radiation Oncology, Zhejiang Provincial People' s Hospital, People' s Hospital of Hangzhou Medical College, Hangzhou, Zhejiang, P.R. China.ORCID 0000-0003-3738-9761
Jiayan LianDepartment of Pathology, The Seventh Affiliated Hospital of Sun Yat-Sen University, Shenzhen, Guangdong, P.R. China.
Sun Yat-sen University · CNZhejiang Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The protein, tripartite motif containing 24 (TRIM24) is a member of the TRIM protein family, and acts as a critical co-regulator of multiple nuclear receptors. TRIM24 is dysregulated in many cancers, including colorectal carcinoma. However, its biological functions and molecular mechanisms with respect to colorectal carcinoma are still largely unknown. In the current study, we found that TRIM24 promotes YAP signaling for driving cell proliferation in colorectal cancer. TRIM24 was significantly upregulated in colorectal carcinoma, and its expression was negatively correlated with the survival of patients. Depletion of TRIM24 impaired the ability of the cancer cells to proliferate and form colonies. Furthermore, this study also revealed the mechanism underlying the recruitment of TRIM24 by the DANCR/KAT6A complex, which is bound to acetylated lysine 23 of histone H3 (H3K23), resulting in binding to the YAP promoter and activation of YAP transcription that ultimately enhances the proliferation of colorectal cancer cells. Our results revealed a novel mechanism involving TRIM24-YAP signaling for the regulation of colorectal cancer. We also identified TRIM24 as a potential therapeutic molecule for targeting colorectal cancer.

Indexed as

Cell ProliferationAdaptor Proteins, Signal TransducingAnimalsCarrier ProteinsCell Line, TumorColorectal NeoplasmsFemaleHippo Signaling PathwayHistone AcetyltransferasesHistonesHumansMiceMice, Inbred BALB CMice, NudeNeoplasm ProteinsProtein Serine-Threonine KinasesAdaptor Proteins, Signal TransducingCarrier ProteinsDANCR long noncoding RNA, humanHistone AcetyltransferasesHistonesKAT6A protein, humanNeoplasm ProteinsProtein Serine-Threonine KinasesRNA, Long NoncodingTranscription FactorsTRIM24 protein, humanYAP1 protein, humanYAP-Signaling ProteinsCell proliferationColorectal cancerTRIM24YAP

Identifiers

PMID32677374
PMCPMC7476840
OpenAlexW3043723636

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.