Evidence map›Paper›PMID 38092725›Full record

ArticleCell death & disease2023

Jagged1 intracellular domain/SMAD3 complex transcriptionally regulates TWIST1 to drive glioma invasion.

Jung Yun Kim, Nayoung Hong, Sehyeon Park, Seok Won Ham, Eun-Jung Kim, Sung-Ok Kim, Junseok Jang, Yoonji Kim, Jun-Kyum Kim, Sung-Chan Kim and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Hypoxia-related THBDJournal of cellular and molecular medicine · 2024
    Article
  9. Article
  10. Article
  11. 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

12 authors at 3 institutions in 1 country.

Jung Yun Kim *Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, 02841, Republic of Korea.ORCID 0000-0002-7331-1710
Nayoung Hong *Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, 02841, Republic of Korea.
Sehyeon ParkDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, 02841, Republic of Korea.
Seok Won HamMEDIFIC Inc., Hwaseong-si, Gyeonggi-do, 18469, Republic of Korea.
Eun-Jung KimMEDIFIC Inc., Hwaseong-si, Gyeonggi-do, 18469, Republic of Korea.
Sung-Ok KimDepartment of Biochemistry, College of Medicine, Hallym University, Chuncheon, 24252, Republic of Korea.
Junseok JangDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, 02841, Republic of Korea.
Yoonji KimDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, 02841, Republic of Korea.
Jun-Kyum KimMEDIFIC Inc., Hwaseong-si, Gyeonggi-do, 18469, Republic of Korea.
Sung-Chan KimDepartment of Biochemistry, College of Medicine, Hallym University, Chuncheon, 24252, Republic of Korea.
Jong-Whi ParkDepartment of Life Sciences, Gachon University, Incheon, 21999, Republic of Korea. jpark@gachon.ac.kr.ORCID 0000-0002-9890-9241
Hyunggee KimDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, 02841, Republic of Korea. hg-kim@korea.ac.kr.ORCID 0000-0002-5164-1663
Korea University · KRHallym University · KRGachon University · KR

Funding

National Research Foundation of Korea (NRF) 2020R1A2C2099668National Research Foundation of Korea (NRF) 2022M3E5F2018255National Research Foundation of Korea (NRF) 2022R1F1A1063909National Research Foundation of Korea (NRF) RS-2023-00208798
6 · The paper itself

Abstract

Jagged1 (JAG1) is a Notch ligand that correlates with tumor progression. Not limited to its function as a ligand, JAG1 can be cleaved, and its intracellular domain translocates to the nucleus, where it functions as a transcriptional cofactor. Previously, we showed that JAG1 intracellular domain (JICD1) forms a protein complex with DDX17/SMAD3/TGIF2. However, the molecular mechanisms underlying JICD1-mediated tumor aggressiveness remains unclear. Here, we demonstrate that JICD1 enhances the invasive phenotypes of glioblastoma cells by transcriptionally activating epithelial-to-mesenchymal transition (EMT)-related genes, especially TWIST1. The inhibition of TWIST1 reduced JICD1-driven tumor aggressiveness. Although SMAD3 is an important component of transforming growth factor (TGF)-β signaling, the JICD1/SMAD3 transcriptional complex was shown to govern brain tumor invasion independent of TGF-β signaling. Moreover, JICD1-TWIST1-MMP2 and MMP9 axes were significantly correlated with clinical outcome of glioblastoma patients. Collectively, we identified the JICD1/SMAD3-TWIST1 axis as a novel inducer of invasive phenotypes in cancer cells.

Indexed as

GlioblastomaCell Line, TumorEpithelial-Mesenchymal TransitionHomeodomain ProteinsHumansJagged-1 ProteinLigandsNuclear ProteinsRepressor ProteinsSignal TransductionSmad3 ProteinTransforming Growth Factor betaTwist-Related Protein 1Homeodomain ProteinsJAG1 protein, humanJagged-1 ProteinLigandsNuclear ProteinsRepressor ProteinsSmad3 ProteinSMAD3 protein, humanTGIF2 protein, humanTransforming Growth Factor betaTWIST1 protein, humanTwist-Related Protein 1

Identifiers

PMID38092725
PMCPMC10719344
OpenAlexW4389685853

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.