Evidence map›Paper›PMID 26447757›Full record

ArticleOncotarget2015

Repurposing of nitroxoline as a potential anticancer agent against human prostate cancer: a crucial role on AMPK/mTOR signaling pathway and the interplay with Chk2 activation.

Wei-Ling Chang, Lih-Ching Hsu, Wohn-Jenn Leu, Ching-Shih Chen, Jih-Hwa Guh

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

28 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  3. Review
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  6. Induction of Programmed Cell Death inAntioxidants (Basel, Switzerland) · 2023
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. AMPK's double-faced role in advanced stages of prostate cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. The roles of PD-1/PD-L1 in the prognosis and immunotherapy of prostate cancer.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Review
  17. Review
  18. Article
  19. Hsa_circ_0086414 Might Be a Diagnostic Biomarker of Oral Squamous Cell Carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  20. Anti-inflammatory Property of AMP-activated Protein Kinase.Anti-inflammatory & anti-allergy agents in medicinal chemistry · 2020
    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

5 authors at 2 institutions in 2 countries.

Wei-Ling ChangThe Division of Medicinal Chemistry, College of Pharmacy, Ohio State University, Columbus, OH 43210, USA.
Lih-Ching HsuSchool of Pharmacy, National Taiwan University, Taipei 100, Taiwan.
Wohn-Jenn LeuSchool of Pharmacy, National Taiwan University, Taipei 100, Taiwan.
Ching-Shih ChenThe Division of Medicinal Chemistry, College of Pharmacy, Ohio State University, Columbus, OH 43210, USA.
Jih-Hwa GuhSchool of Pharmacy, National Taiwan University, Taipei 100, Taiwan.
National Taiwan University · TWThe Ohio State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nitroxoline is an antibiotic by chelating Zn2+ and Fe2+ from biofilm matrix. In this study, nitroxoline induced G1 arrest of cell cycle and subsequent apoptosis in prostate cancer cells through ion chelating-independent pathway. It decreased protein levels of cyclin D1, Cdc25A and phosphorylated Rb, but activated AMP-activated protein kinase (AMPK), a cellular energy sensor and signal transducer, leading to inhibition of downstream mTOR-p70S6K signaling. Knockdown of AMPKα significantly rescued nitroxoline-induced inhibition of cyclin D1-Rb-Cdc25A axis indicating AMPK-dependent mechanism. However, cytoprotective autophagy was simultaneously evoked by nitroxoline. Comet assay and Western blot analysis demonstrated DNA damaging effect and activation of Chk2 other than Chk1 to nitroxoline action. Instead of serving as a DNA repair transducer, nitroxoline-mediated Chk2 activation was identified to function as a pro-apoptotic inducer. In conclusion, the data suggest that nitroxoline induces anticancer activity through AMPK-dependent inhibition of mTOR-p70S6K signaling pathway and cyclin D1-Rb-Cdc25A axis, leading to G1 arrest of cell cycle and apoptosis. AMPK-dependent activation of Chk2, at least partly, contributes to apoptosis. The data suggest the potential role of nitroxoline for therapeutic development against prostate cancers.

Indexed as

AMP-Activated Protein KinasesAntineoplastic AgentsApoptosisBlotting, Westerncdc25 PhosphatasesCell Line, TumorCell ProliferationCheckpoint Kinase 2Cyclin D1DNA DamageDrug RepositioningEnzyme ActivationG1 Phase Cell Cycle CheckpointsHumansMaleMicroscopy, FluorescenceAMP-Activated Protein KinasesAntineoplastic AgentsCDC25A protein, humancdc25 PhosphatasesCheckpoint Kinase 2CHEK2 protein, humanCyclin D1NitroquinolinesnitroxolineRetinoblastoma ProteinTOR Serine-Threonine KinasesAMPK/mTOR signalingChk2Cyclin D1-Rb-Cdc25A axisG1 arrestNitroxoline

Identifiers

PMID26447757
PMCPMC4741862
OpenAlexW2173889361

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.