Evidence map›Paper›PMID 31908141›Full record

ArticleEMBO reports2020

PCAF-mediated acetylation of ISX recruits BRD4 to promote epithelial-mesenchymal transition.

Li-Ting Wang, Kwei-Yan Liu, Wen-Yih Jeng, Cheng-Ming Chiang, Chee-Yin Chai, Shyh-Shin Chiou, Ming-Shyang Huang, Kazunari K Yokoyama, Shen-Nien Wang, Shau-Ku Huang and 1 more

Open access · hybridAbstract read
In one paragraph

Article in EMBO reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

37 citing papers in PubMed, 44 citations in OpenAlex.

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  10. Reversible Acetylation of Non-histone Proteins in Human Cancers.Results and problems in cell differentiation · 2025
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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

11 authors at 5 institutions in 4 countries.

Li-Ting WangGraduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Kwei-Yan LiuDepartment of Respirology & Allergy, Third Affiliated Hospital of Shenzhen University, Shenzhen, China.
Wen-Yih JengUniversity Center for Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan.
Cheng-Ming ChiangDepartment of Biochemistry, and Department of Pharmacology, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Chee-Yin ChaiDepartment of Pathology, Faculty of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Shyh-Shin ChiouCenter of Applied Genomics, Kaohsiung Medical University, Kaohsiung, Taiwan.
Ming-Shyang HuangDepartment of Internal Medicine, E-Da Cancer Hospital, School of Medicine, I-Shou University, Kaohsiung, Taiwan.
Kazunari K YokoyamaGraduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.ORCID 0000-0001-8508-7587
Shen-Nien WangGraduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Shau-Ku HuangDepartment of Respirology & Allergy, Third Affiliated Hospital of Shenzhen University, Shenzhen, China.
Shih-Hsien HsuGraduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.ORCID 0000-0003-2102-0505
Kaohsiung Medical University · TWI-Shou University · TWJohns Hopkins University · USNational Cheng Kung University · TWThe University of Texas Southwestern Medical Center · US

Funding

E2-Cellular Complexes in HPV Chromatin TranscriptionR01CA103867 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI CHIANG, CHENG-MING · 2004 to 2017
$4.0M
Opposing Functions of BRD4 Isoforms in Breast CancerR01CA251698 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI CHIANG, CHENG-MING · 2020 to 2024
$2.3M
Cancer Prevention & Research Institute of Texas CPRIT RP180349Cancer Prevention & Research Institute of Texas RP190077Kaohsiung Medical University Chung-Ho Memorial Hospital (KMUH) KMUH-106-6R33Kaohsiung Medical University Chung-Ho Memorial Hospital (KMUH) KMUH107-7R34Kaohsiung Medical University Chung-Ho Memorial Hospital (KMUH) KMUH107-7R46Kaohsiung Medical University Chung-Ho Memorial Hospital (KMUH) KMU-TC108A04-5Kaohsiung Medical University (KMU) 106KMUOR04Kaohsiung Medical University (KMU) KMU-DK108012Kaohsiung Medical University (KMU) KMU-TC108A02Ministry of Science and Technology, Taiwan (MOST) MOST-105-2314-B-037-70-MY2Ministry of Science and Technology, Taiwan (MOST) MOST-106-2314-B-037-090-MY2Ministry of Science and Technology, Taiwan (MOST) MOST-107-2314-B-037-028-MY3Ministry of Science and Technology, Taiwan (MOST) MOST-107-2314-B-037-063-MY3Ministry of Science and Technology, Taiwan (MOST) MOST-108-2314-B-037-065-MY3Ministry of Science and Technology, Taiwan (MOST) MOST-108-2320-B-037-005National Health Research Institutes (NHRI) EOPP10-014National Health Research Institutes (NHRI) NHRI-EX108-10720SINCI NIH HHS R01 CA103867NCI NIH HHS R01 CA251698Shenzhen Science and Technology Peacock Team Project KQTD20170331145453160Welch Foundation I-1805
6 · The paper itself

Abstract

Epigenetic regulation is important for cancer progression; however, the underlying mechanisms, particularly those involving protein acetylation, remain to be fully understood. Here, we show that p300/CBP-associated factor (PCAF)-dependent acetylation of the transcription factor intestine-specific homeobox (ISX) regulates epithelial-mesenchymal transition (EMT) and promotes cancer metastasis. Mechanistically, PCAF acetylation of ISX at lysine 69 promotes the interaction with acetylated bromodomain-containing protein 4 (BRD4) at lysine 332 in tumor cells, and the translocation of the resulting complex into the nucleus. There, it binds to promoters of EMT genes, where acetylation of histone 3 at lysines 9, 14, and 18 initiates chromatin remodeling and subsequent transcriptional activation. Ectopic ISX expression enhances EMT marker expression, including TWIST1, Snail1, and VEGF, induces cancer metastasis, but suppresses E-cadherin expression. In lung cancer, ectopic expression of PCAF-ISX-BRD4 axis components correlates with clinical metastatic features and poor prognosis. These results suggest that the PCAF-ISX-BRD4 axis mediates EMT signaling and regulates tumor initiation and metastasis.

Indexed as

Epithelial-Mesenchymal TransitionNeoplasmsTranscription FactorsAcetylationEpigenesis, GeneticGenes, HomeoboxHumansNuclear Proteinsp300-CBP Transcription FactorsNuclear Proteinsp300-CBP Transcription FactorsTranscription FactorsBRD4EMTISXTWIST1

Identifiers

PMID31908141
PMCPMC7001155
OpenAlexW2998851706

What OpenQuestion holds

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LicenceCC BY
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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.