Evidence map›Paper›PMID 30389290›Full record

ArticleBioorganic & medicinal chemistry letters2018

Analogs of penfluridol as chemotherapeutic agents with reduced central nervous system activity.

Md Ashraf-Uz-Zaman, Md Sanaullah Sajib, Luca Cucullo, Constantinos M Mikelis, Nadezhda A German

Open access · greenAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Drug repositioning: examining antipsychotic drugs and their anticancer effects.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Low Dose of Penfluridol Inhibits VEGF-Induced Angiogenesis.International journal of molecular sciences · 2020
    Article
  10. 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 1 institution in 1 country.

Md Ashraf-Uz-ZamanDepartment of Pharmaceutical Sciences, Texas Tech University Health Sciences Center, School of Pharmacy, Amarillo, TX 79106, United States.
Md Sanaullah SajibDepartment of Pharmaceutical Sciences, Texas Tech University Health Sciences Center, School of Pharmacy, Amarillo, TX 79106, United States.
Luca CuculloDepartment of Pharmaceutical Sciences, Texas Tech University Health Sciences Center, School of Pharmacy, Amarillo, TX 79106, United States.
Constantinos M MikelisDepartment of Pharmaceutical Sciences, Texas Tech University Health Sciences Center, School of Pharmacy, Amarillo, TX 79106, United States.
Nadezhda A GermanDepartment of Pharmaceutical Sciences, Texas Tech University Health Sciences Center, School of Pharmacy, Amarillo, TX 79106, United States. Electronic address: nadezhda.german@ttuhsc.edu.
Texas Tech University · US

Funding

Testing tobacco smoke toxicity at the blood-brain barrierR01DA029121 · NIDA · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI ABBRUSCATO, THOMAS J, CUCULLO, LUCA · 2011 to 2021
$3.6M
Novel Class of Chemotherapeutic Agents for Treatment of Metastatic Triple-negative Breast CancerR15CA231339 · NCI · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI GERMAN, NADEZHDA A, MIKELIS, CONSTANTINOS MARIOS · 2018 to 2018
$459k
NCI NIH HHS R15 CA231339NIDA NIH HHS R01 DA029121
6 · The paper itself

Abstract

Several recent reports have highlighted the feasibility of the use of penfluridol, a well-known antipsychotic agent, as a chemotherapeutic agent. In vivo experiments have confirmed the cytotoxic activity of penfluridol in triple-negative breast cancer model, lung cancer model, and further studies have been proposed to assess its anticancer activity and viability for the treatment of glioblastomas. However, penfluridol anticancer activity was observed at a dosage significantly higher than that administered in antipsychotic therapy, thus raising the concern for the potential onset of CNS side effects in patients undergoing intensive pharmacological treatment. In this study, we evaluate the potential CNS toxicity of penfluridol side by side with a set of analogs.

Indexed as

AnimalsAntineoplastic AgentsAntipsychotic AgentsCell Line, TumorCell SurvivalCentral Nervous SystemDisease Models, AnimalFemaleHumansLung NeoplasmsMiceMice, Inbred C57BLPenfluridolProtein BindingReceptors, G-Protein-CoupledStructure-Activity RelationshipAntineoplastic AgentsAntipsychotic AgentsPenfluridolReceptors, G-Protein-CoupledAnticancer agentCentral nervous systemOptimizationPenfluridolRepurposingToxicity

Identifiers

PMID30389290
PMCPMC6438620
OpenAlexW2898362500

What OpenQuestion holds

Textmetadata
LicenceTDM
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.