Evidence map›Paper›PMID 31960187›Full record

ReviewJournal of cancer research and clinical oncology2020

"Hedgehog pathway": a potential target of itraconazole in the treatment of cancer.

Xin Wei, Wu Liu, Jia Qi Wang, Zeyao Tang

Open access · greenAbstract readReview
In one paragraph

Review in Journal of cancer research and clinical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Emerging Applications of Triazole Antifungal Drugs.International journal of molecular sciences · 2026
    Review
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  6. Review
  7. Article
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  9. Review
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  11. Article
  12. Article
  13. Article
  14. A Systematic Review of Artificial Intelligence Techniques in Cancer Prediction and Diagnosis.Archives of computational methods in engineering : state of the art reviews · 2022
    Review
  15. Article
  16. Review
  17. Enhancing theDrug delivery · 2021
    Article
  18. Article
  19. Review
  20. 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

4 authors at 2 institutions in 1 country.

Xin WeiAcad Integrated Med & College of Pharmacy, Department of Pharmacy, Dalian Medical University, Dalian, 116044, People's Republic of China.
Wu LiuAcad Integrated Med & College of Pharmacy, Department of Pharmacy, Dalian Medical University, Dalian, 116044, People's Republic of China.
Jia Qi WangDepartment of Plastic and Reconstructive Surgery, The First Bethune Hospital of Jilin University, Chang Chun, 130021, People's Republic of China.
Zeyao TangAcad Integrated Med & College of Pharmacy, Department of Pharmacy, Dalian Medical University, Dalian, 116044, People's Republic of China. tangzeyao@aliyun.com.ORCID http://orcid.org/0000-0003-2412-5871
Dalian Medical University · CNFirst Bethune Hospital of Jilin University · CN

Funding

Natural Science Foundation of China 30772601University Innovation Team Project Foundation of Education Department of Liaoning Province LT2013019
6 · The paper itself

Abstract

purposeItraconazole is an antifungal drug that has been clinically used for over 30 years. In recent years, scholars have discovered that it possesses an anticancer effect. Moreover, its mechanism has been clarified to some degree. What deserves to be mentioned is that itraconazole acting on the Hedgehog pathway has made a new progress in the treatment of cancers. While interestingly, studies have demonstrated that the Hedgehog pathway is largely activated in different cancer cells.

resultThis review tries to highlight the effect of itraconazole on smoothened receptor (SMO) in the Hedgehog pathway, thereby reducing the glioma-associated oncogene homolog (GLI) release and finally exhibiting a range of anticancer effects, promoting apoptosis of cancer cells, and inhibiting proliferation by indirect inhibition of NF-κB pathway and inflammation, moreover, promoting the expression of cyclin-dependent kinase inhibitors, inhibiting the expression of target genes transcribed by GLI such as BCL-2 and Cyclin-D1. Besides, itraconazole increases the number of Bnip3, subsequently, inducing the dissociation of the Beclin-1/BCL-2 binding complex, as a result of ultimately promoting autophagy of cancer cells.

conclusionAs a new anticancer drug, whether itraconazole eventually entering clinical application requires the joint eforts of all scholars. In any case, an in-depth study on itraconazole will bring new hope for cancer patients in the near future.

Indexed as

AnimalsClinical Trials, Phase II as TopicHedgehog ProteinsHumansItraconazoleMolecular Targeted TherapyNeoplasmsRandomized Controlled Trials as TopicSignal TransductionSmoothened ReceptorHedgehog ProteinsItraconazoleSmoothened ReceptorApoptosisAutophagyCyclin-dependent kinase inhibitorsHedgehog pathwayItraconazole

Identifiers

PMID31960187
PMCPMC11804422
OpenAlexW3000670599

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.