Evidence map›Paper›PMID 27102442›Full record

ArticleOncotarget2016

JMJD3 promotes survival of diffuse large B-cell lymphoma subtypes via distinct mechanisms.

Yan Zhang, Long Shen, Dwayne G Stupack, Nan Bai, Jing Xun, Guosheng Ren, Jihong Han, Luyuan Li, Yunping Luo, Rong Xiang and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. JMJD family proteins in cancer and inflammation.Signal transduction and targeted therapy · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. The Functions of the Demethylase JMJD3 in Cancer.International journal of molecular sciences · 2021
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  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

11 authors at 5 institutions in 2 countries.

Yan ZhangDepartment of Immunology, Medical School of Nankai University, Tianjin 300071, China.
Long ShenDepartment of Pathology, Medical School of Nankai University, Tianjin 300071, China.
Dwayne G StupackUCSD Moores Cancer Center, University of California, San Diego, La Jolla CA 92093, USA.
Nan BaiDepartment of Immunology, Medical School of Nankai University, Tianjin 300071, China.
Jing XunDepartment of Pathology, Medical School of Nankai University, Tianjin 300071, China.
Guosheng RenMolecular Oncology and Epigenetics Laboratory, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Jihong HanThe College of Life Sciences, Nankai University, Tianjin 300071, China.
Luyuan LiThe College of Life Sciences, Nankai University, Tianjin 300071, China.
Yunping LuoDepartment of Immunology, Beijing Union Medical School, Beijing, 100010, China.
Rong XiangDepartment of Immunology, Medical School of Nankai University, Tianjin 300071, China.
Xiaoyue TanDepartment of Pathology, Medical School of Nankai University, Tianjin 300071, China.
Nankai University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNChongqing Medical University · CNLogistics University of People's Armed Police Force · CNUniversity of California, San Diego · US

Funding

Integrins and Caspase 8 in Tumor ProgressionR01CA107263 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI STUPACK, DWAYNE G. · 2005 to 2014
$3.1M
NCI NIH HHS R01 CA107263
6 · The paper itself

Abstract

JMJD3 (Jumonji domain containing-3), a histone H3 Lys27 (H3K27) demethylase, has been reported to be involved in the antigen-driven differentiation of germinal center B-cells. However, insight into the mechanism of JMJD3 in DLBCL (Diffuse large B-cell lymphoma) progression remains poorly understood. In this study, we investigated the subtype-specific JMJD3-dependent survival effects in DLBCL. Our data showed that in the ABC subtype, silencing-down of JMJD3 inhibited interferon regulatory factor 4 (IRF4) expression in a demethylase activity-dependent fashion. IRF4 reciprocally stimulated expression of JMJD3, forming a positive feedback loop that promoted survival in these cells. Accordingly, IRF4 expression was sufficient to rescue the pro-apoptotic effect of JMJD3 suppression in the ABC, but not in the GCB subtype. In contrast, ectopic overexpression of BCL-2 completely offset JMJD3-mediated survival in the GCB DLBCL cells. In vivo, treatment with siRNA to JMJD3 reduced tumor volume concordant with increased apoptosis in either subtype. This suggests it is a common target, though the distinctive signaling axes regulating DCBCL survival offer different strategic options for treating DLBCL subtypes.

Indexed as

AnimalsApoptosisHeterograftsHumansJumonji Domain-Containing Histone DemethylasesLymphoma, Large B-Cell, DiffuseMiceMice, Inbred NODMice, SCIDTumor Cells, CulturedJumonji Domain-Containing Histone DemethylasesKDM6B protein, humanapoptosisBcl-2DLBCLIRF4JMJD3

Identifiers

PMID27102442
PMCPMC5045403
OpenAlexW2340879982

What OpenQuestion holds

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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.