Evidence map›Paper›PMID 38653754›Full record

ArticleSignal transduction and targeted therapy2024

SRY-Box transcription factor 9 triggers YAP nuclear entry via direct interaction in tumors.

Hui Qian, Chen-Hong Ding, Fang Liu, Shi-Jie Chen, Chen-Kai Huang, Meng-Chao Xiao, Xia-Lu Hong, Ming-Chen Wang, Fang-Zhi Yan, Kai Ding and 6 more

Open access · goldAbstract read
In one paragraph

Article in Signal transduction and targeted therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

17 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Mechanobiological Strategies to Enhance Ovine (Animals : an open access journal from MDPI · 2024
    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 4 institutions in 1 country.

Hui Qian *Department of Gastroenterology, Changzheng Hospital, Naval Medical University, Shanghai, China.
Chen-Hong Ding *Department of Gastroenterology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, China.
Fang Liu *Department of Gastroenterology, Changzheng Hospital, Naval Medical University, Shanghai, China.
Shi-Jie Chen *Drug Discovery and Design Center, CAS Key Laboratory of Receptor Research, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Chen-Kai HuangDepartment of Gastroenterology, First Affiliated Hospital of Nanchang University, Nanchang, China.
Meng-Chao XiaoDepartment of Gastroenterology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, China.
Xia-Lu HongDepartment of Gastroenterology, Changzheng Hospital, Naval Medical University, Shanghai, China.
Ming-Chen WangDrug Discovery and Design Center, CAS Key Laboratory of Receptor Research, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Fang-Zhi YanDepartment of Gastroenterology, Changzheng Hospital, Naval Medical University, Shanghai, China.
Kai DingDepartment of Gastroenterology, Changzheng Hospital, Naval Medical University, Shanghai, China.
Ya-Lu CuiDepartment of Gastroenterology, Changzheng Hospital, Naval Medical University, Shanghai, China.
Bai-Nan ZhengDepartment of Gastroenterology, Changzheng Hospital, Naval Medical University, Shanghai, China.
Jin DingClinical Cancer Institute, Center for Translational Medicine, Naval Medical University, Shanghai, China.
Cheng LuoDrug Discovery and Design Center, CAS Key Laboratory of Receptor Research, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China. cluo@simm.ac.cn.ORCID 0000-0003-3864-8382
Xin ZhangDepartment of Gastroenterology, Changzheng Hospital, Naval Medical University, Shanghai, China. zhang68@hotmail.com.
Wei-Fen XieDepartment of Gastroenterology, Changzheng Hospital, Naval Medical University, Shanghai, China. weifenxie@medmail.com.cn.
Shanghai Changzheng Hospital · CNChinese Academy of Sciences · CNShanghai East Hospital · CNNanchang University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81703415National Natural Science Foundation of China (National Science Foundation of China) 81802324National Natural Science Foundation of China (National Science Foundation of China) 81900514National Natural Science Foundation of China (National Science Foundation of China) 82030021National Natural Science Foundation of China (National Science Foundation of China) 82070620National Natural Science Foundation of China (National Science Foundation of China) 82072641National Natural Science Foundation of China (National Science Foundation of China) 91853205
6 · The paper itself

Abstract

The translocation of YAP from the cytoplasm to the nucleus is critical for its activation and plays a key role in tumor progression. However, the precise molecular mechanisms governing the nuclear import of YAP are not fully understood. In this study, we have uncovered a crucial role of SOX9 in the activation of YAP. SOX9 promotes the nuclear translocation of YAP by direct interaction. Importantly, we have identified that the binding between Asp-125 of SOX9 and Arg-124 of YAP is essential for SOX9-YAP interaction and subsequent nuclear entry of YAP. Additionally, we have discovered a novel asymmetrical dimethylation of YAP at Arg-124 (YAP-R124me2a) catalyzed by PRMT1. YAP-R124me2a enhances the interaction between YAP and SOX9 and is associated with poor prognosis in multiple cancers. Furthermore, we disrupted the interaction between SOX9 and YAP using a competitive peptide, S-A1, which mimics an α-helix of SOX9 containing Asp-125. S-A1 significantly inhibits YAP nuclear translocation and effectively suppresses tumor growth. This study provides the first evidence of SOX9 as a pivotal regulator driving YAP nuclear translocation and presents a potential therapeutic strategy for YAP-driven human cancers by targeting SOX9-YAP interaction.

Indexed as

Adaptor Proteins, Signal TransducingCell NucleusSOX9 Transcription FactorTranscription FactorsYAP-Signaling ProteinsActive Transport, Cell NucleusAnimalsCell Line, TumorHumansMiceNeoplasmsProtein-Arginine N-MethyltransferasesRepressor ProteinsAdaptor Proteins, Signal TransducingPRMT1 protein, humanProtein-Arginine N-MethyltransferasesRepressor ProteinsSOX9 protein, humanSOX9 Transcription FactorTranscription FactorsYAP1 protein, humanYAP-Signaling Proteins

Identifiers

PMID38653754
PMCPMC11039692
OpenAlexW4395025759

What OpenQuestion 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 OpenQuestion graph.