Evidence map›Paper›PMID 33637682›Full record

ArticleOncogenesis2021

Epigenetic regulation of TGF-β-induced EMT by JMJD3/KDM6B histone H3K27 demethylase.

Su-Hyun Lee, Okhwa Kim, Hyo-Jin Kim, Cheol Hwangbo, Jeong-Hyung Lee

Open access · goldAbstract read
In one paragraph

Article in Oncogenesis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Impact of KRAS mutation on the tumor microenvironment in colorectal cancer.International journal of biological sciences · 2024
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Methyltransferase Inhibition Enables TgfMolecular and cellular biology · 2023
    Article
  18. Review
  19. JMJD family proteins in cancer and inflammation.Signal transduction and targeted therapy · 2022
    Review
  20. 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

5 authors at 2 institutions in 1 country.

Su-Hyun LeeDepartment of Biochemistry, Kangwon National University, Chuncheon, Gangwon-do, 24341, Republic of Korea.
Okhwa KimDepartment of Biochemistry, Kangwon National University, Chuncheon, Gangwon-do, 24341, Republic of Korea.
Hyo-Jin KimDivision of Applied Life Science (BK21), PMBBRC and Research Institute of Life Sciences, Gyeongsang National University, Jinju, Gyeongsangnam-do, 52828, Republic of Korea.
Cheol Hwangbo *Division of Applied Life Science (BK21), PMBBRC and Research Institute of Life Sciences, Gyeongsang National University, Jinju, Gyeongsangnam-do, 52828, Republic of Korea. chwangbo@gnu.ac.kr.ORCID http://orcid.org/0000-0001-6505-3080
Jeong-Hyung Lee *Department of Biochemistry, Kangwon National University, Chuncheon, Gangwon-do, 24341, Republic of Korea. Jhlee36@kangwon.ac.kr.ORCID http://orcid.org/0000-0003-2651-1645
Kangwon National University · KRGyeongsang National University · KR

Funding

National Research Foundation of Korea (NRF) NRF-2017R1C1B5077066National Research Foundation of Korea (NRF) NRF-2018R1C1B6007728National Research Foundation of Korea (NRF) NRF-2018R1D1A1B07047187National Research Foundation of Korea (NRF) NRF-2020R1A5A8019180
6 · The paper itself

Abstract

Transforming growth factor-β (TGF-β) signaling pathways are well-recognized for their role in proliferation and epithelial-mesenchymal transition (EMT) of cancer cells, but much less is understood about their contribution to interactions with other signaling events. Recent studies have indicated that crosstalk between TGF-β and Ras signaling makes a contribution to TGF-β-mediated EMT. Here, we demonstrate that Jumonji domain containing-3 (JMJD3 also called KDM6B) promotes TGF-β-mediated Smad activation and EMT in Ras-activated lung cancer cells. JMJD3 in lung cancer patients was significantly increased and JMJD3 expression in lung tumor tissues was correlated with expression of K-Ras or H-Ras in particular, and its expression was regulated by Ras activity in lung cancer cells. JMJD3 promotes TGF-β-induced Smad activation and EMT in Ras-activated lung cancer cells through the induction of syntenin, a protein that regulates TGF-β receptor activation upon ligand binding. Tissue array and ChIP analysis revealed that JMJD3 epigenetically induces syntenin expression by directly regulating H3K27 methylation levels. Mechanical exploration identified a physical and functional association of JMJD3 with syntenin presiding over the TGF-β in Ras-activated lung cancer cells. Taken together, these findings provide new insight into the mechanisms by which JMJD3 promotes syntenin expression resulting in oncogenic Ras cooperation with TGF-β to promote EMT.

Identifiers

PMID33637682
PMCPMC7910473
OpenAlexW3130651916

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.