Evidence map›Paper›PMID 31218225›Full record

ArticleBioMed research international2019

Copper (II) Ions Activate Ligand-Independent Receptor Tyrosine Kinase (RTK) Signaling Pathway.

Fang He, Cong Chang, Bowen Liu, Zhu Li, Hao Li, Na Cai, Hong-Hui Wang

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

40 citing papers in PubMed, 56 citations in OpenAlex.

  1. Copper, cuproptosis, and cancer: biology concepts of a novel cell death.Apoptosis : an international journal on programmed cell death · 2026
    Review
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  4. Programmed cell death in lung cancer: mechanisms, immune responses, and therapeutics.Apoptosis : an international journal on programmed cell death · 2026
    Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Menstrual Effluent Derived Immune Cell Composition Is Distinct in Women Using Contraceptives: A Pilot Study.American journal of reproductive immunology (New York, N.Y. : 1989) · 2025
    Article
  11. Review
  12. Article
  13. Review
  14. Cuproplasia and cuproptosis, two sides of the coin.Cancer communications (London, England) · 2025
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Assessment of the Impact of Trace Essential Metals on Cancer Development.International journal of molecular sciences · 2024
    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

7 authors at 1 institution in 1 country.

Fang HeInstitute of Nanotechnology and Tissue Engineering, College of Biology, Hunan University, Changsha, 410082, China.
Cong ChangInstitute of Nanotechnology and Tissue Engineering, College of Biology, Hunan University, Changsha, 410082, China.
Bowen LiuInstitute of Nanotechnology and Tissue Engineering, College of Biology, Hunan University, Changsha, 410082, China.
Zhu LiCellWay Bio, Changsha, 410000, China.
Hao LiState Key Laboratory of Chemo/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, China.
Na CaiCellWay Bio, Changsha, 410000, China.ORCID 0000-0003-2140-471X
Hong-Hui WangInstitute of Nanotechnology and Tissue Engineering, College of Biology, Hunan University, Changsha, 410082, China.ORCID 0000-0002-4420-9733
Hunan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Receptor tyrosine kinase (RTK) is activated by its natural ligand, mediating multiple essential biological processes. Copper (II) ions are bioactive ions and are crucial in the regulation of cell signaling pathway. However, the crosstalk between copper (II) ions and RTK-mediated cellular signaling remains unclear. Herein, we reported the effect of copper (II) ions on the ligand-independent RTK cellular signaling pathway. Our results indicate that both EGFR and MET signaling were activated by copper (II) in the absence of the corresponding ligands, EGF and HGF, respectively. Consequently, copper (II) ions initiate two RTK-mediated downstream signal transductions, including AKT and ERK. Moreover, copper (II) significantly increased proliferation and cellular migration. Our study proposes a novel role of copper in RTK-mediated signaling for growth factor-independent cancer cell proliferation and migration, implying that targeting both the copper (II) and growth factor in tumor microenvironments may be necessary for cancer treatment.

Indexed as

Cell Line, TumorCell MovementCell ProliferationCopperEnzyme ActivationErbB ReceptorsHumansMAP Kinase Signaling SystemProto-Oncogene Proteins c-metCopperEGFR protein, humanErbB ReceptorsMET protein, humanProto-Oncogene Proteins c-met

Identifiers

PMID31218225
PMCPMC6537018
OpenAlexW2946236541

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.