Evidence map›Paper›PMID 28960574›Full record

ReviewProtein science : a publication of the Protein Society2017

Bacterial cupredoxin azurin hijacks cellular signaling networks: Protein-protein interactions and cancer therapy.

Meng Gao, Jingjing Zhou, Zhengding Su, Yongqi Huang

Open access · bronzeAbstract readReview
In one paragraph

Review in Protein science : a publication of the Protein Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Genetic mutations enhance the production of Exotoxin A byExperimental and therapeutic medicine · 2025
    Article
  6. Article
  7. The Production of Recombinant Azurin fromInternational journal of molecular sciences · 2025
    Article
  8. Combination of magnetic hyperthermia and gene therapy for breast cancer.Apoptosis : an international journal on programmed cell death · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Cells · 2023
    Review
  17. Review
  18. Review
  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

4 authors at 1 institution in 1 country.

Meng GaoInstitute of Biomedical and Pharmaceutical Sciences, Hubei University of Technology, Wuhan, China.
Jingjing ZhouInstitute of Biomedical and Pharmaceutical Sciences, Hubei University of Technology, Wuhan, China.
Zhengding SuInstitute of Biomedical and Pharmaceutical Sciences, Hubei University of Technology, Wuhan, China.
Yongqi HuangInstitute of Biomedical and Pharmaceutical Sciences, Hubei University of Technology, Wuhan, China.ORCID http://orcid.org/0000-0002-9463-8325
Wuhan University of Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Azurin secreted by Pseudomonas aeruginosa is an anticancer bacteriocin, which preferentially enters human cancer cells and induces apoptosis or growth inhibition. It turns out that azurin is a multi-target anticancer agent interfering in the p53 signaling pathway and the non-receptor tyrosine kinases signaling pathway. This suggests that azurin exerts its anticancer activity by interacting with multiple targets and interfering in multiple steps in disease progression. Therefore, azurin could overcome resistance to therapy. Besides azurin, putative bacteriocins that possess functional properties similar to those of azurin have been identified in more bacteria species. A systematic investigation on the anticancer mechanisms of azurin and the azurin-like bacteriocins will provide more and better options in cancer therapy. In this review, we summarize how azurin and the derived peptides hijack key cellular regulators or cell surface receptors to remodel the cellular signaling networks. In particular, we highlight the necessity of determining the structure of azurin/p53 complex and investigating the influence of post-translational modifications on interactions between azurin and p53. Therapeutic applications of azurin and derived peptides are also discussed.

Indexed as

AnimalsAntineoplastic AgentsAzurinBacterial ProteinsCell Line, TumorHumansMCF-7 CellsMiceProtein Processing, Post-TranslationalPseudomonas aeruginosaSignal TransductionTumor Suppressor Protein p53Antineoplastic AgentsAzurinBacterial ProteinscupredoxinTumor Suppressor Protein p53Anticancer drugsbacterial proteinsnon-receptor tyrosine kinasesp53tumor suppression

Identifiers

PMID28960574
PMCPMC5699490
OpenAlexW2758628216

What OpenQuestion holds

Textmetadata
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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.