Evidence map›Paper›PMID 30967636›Full record

ArticleOncogene2019

JMJD2 promotes acquired cisplatin resistance in non-small cell lung carcinoma cells.

Lei Duan, Ricardo E Perez, Paul D Chastain, Mathew T Mathew, Divya Rani Bijukumar, Carl G Maki

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. [CT radiomicsZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
    Article
  3. Article
  4. ATR expression as a prognostic biomarker inJournal of thoracic disease · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. [Research Progress of DNA Methylation in Cisplatin Resistance in Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2023
    Review
  12. Article
  13. JMJD family proteins in cancer and inflammation.Signal transduction and targeted therapy · 2022
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. The Influence of Cell Cycle Regulation on Chemotherapy.International journal of molecular sciences · 2021
    Review
  19. Article
  20. [Cell Cycle Checkpoint Kinase and Drug Resistance of Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2021
    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

6 authors at 3 institutions in 1 country.

Lei DuanDepartment of Cell & Molecular Medicine, Rush University Medical Center, Chicago, IL, 60612, USA.
Ricardo E PerezDepartment of Cell & Molecular Medicine, Rush University Medical Center, Chicago, IL, 60612, USA.
Paul D ChastainDepartment of Health Sciences Education, University of Illinois College of Medicine at Rockford, Rockford, IL, 61107, USA.
Mathew T MathewDepartment of Biomedical Sciences, University of Illinois College of Medicine at Rockford, Rockford, IL, 61107, USA.
Divya Rani BijukumarDepartment of Biomedical Sciences, University of Illinois College of Medicine at Rockford, Rockford, IL, 61107, USA.
Carl G MakiDepartment of Cell & Molecular Medicine, Rush University Medical Center, Chicago, IL, 60612, USA. Carl_Maki@rush.edu.
Rush University Medical Center · USIllinois College · USUniversity of Illinois Chicago, Rockford campus · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Platinum-based drugs such as cisplatin (CP) are the first-line chemotherapy for non-small-cell lung carcinoma (NSCLC). Unfortunately, NSCLC has a low response rate to CP and acquired resistance always occurs. Histone methylation regulates chromatin structure and is implicated in DNA repair. We hypothesize histone methylation regulators are involved in CP resistance. We therefore screened gene expression of known histone methyltransferases and demethylases in three NSCLC cell lines with or without acquired resistance to CP. JMJD2s are a family of histone demethylases that remove tri-methyl groups from H3K9 and H3K36. We found expression of several JMJD2 family genes upregulated in CP-resistant cells, with JMJD2B expression being upregulated in all three CP-resistant NSCLC cell lines. Further analysis showed increased JMJD2 protein expression coincided with decreased H3K9me3 and H3K36me3. Chemical inhibitors of JMJD2-family proteins increased H3K9me3 and H3K36me3 levels and sensitized resistant cells to CP. Mechanistic studies showed that JMJD2 inhibition decreased chromatin association of ATR and Chk1 and inhibited the ATR-Chk1 replication checkpoint. Our results reveal that JMJD2 demethylases are potential therapeutic targets to overcome CP resistance in NSCLC.

Indexed as

Drug Resistance, NeoplasmAntineoplastic AgentsAtaxia Telangiectasia Mutated ProteinsCarcinoma, Non-Small-Cell LungCell Line, TumorCheckpoint Kinase 1CisplatinHistonesHumansJumonji Domain-Containing Histone DemethylasesLung NeoplasmsMethylationAntineoplastic AgentsAtaxia Telangiectasia Mutated ProteinsATR protein, humanCheckpoint Kinase 1CHEK1 protein, humanCisplatinHistonesJumonji Domain-Containing Histone Demethylases

Identifiers

PMID30967636
OpenAlexW2937479924

What OpenQuestion holds

Textmetadata
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.