Evidence map›Paper›PMID 24895612›Full record

ReviewBioMed research international2014

Evaluating the cancer therapeutic potential of cardiac glycosides.

José Manuel Calderón-Montaño, Estefanía Burgos-Morón, Manuel Luis Orta, Dolores Maldonado-Navas, Irene García-Domínguez, Miguel López-Lázaro

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 121 citations in OpenAlex.

  1. Pharmaceuticals (Basel, Switzerland) · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Flavonoids as Potential Natural Compounds for the Prevention and Treatment of Eczema.Anti-inflammatory & anti-allergy agents in medicinal chemistry · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Cardiac glycosides fromRSC advances · 2022
    Article
  16. Article
  17. The botanical drug PBI-05204, a supercritical COFrontiers in pharmacology · 2022
    Article
  18. Article
  19. Article
  20. Bulbous PlantsPharmaceutics · 2021
    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

6 authors at 1 institution in 1 country.

José Manuel Calderón-MontañoDepartment of Pharmacology, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.
Estefanía Burgos-MorónDepartment of Pharmacology, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.
Manuel Luis OrtaDepartment of Cell Biology, Faculty of Biology, University of Seville, Spain.
Dolores Maldonado-NavasDepartment of Pharmacology, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.
Irene García-DomínguezDepartment of Pharmacology, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.
Miguel López-LázaroDepartment of Pharmacology, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.
Universidad de Sevilla · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiac glycosides, also known as cardiotonic steroids, are a group of natural products that share a steroid-like structure with an unsaturated lactone ring and the ability to induce cardiotonic effects mediated by a selective inhibition of the Na(+)/K(+)-ATPase. Cardiac glycosides have been used for many years in the treatment of cardiac congestion and some types of cardiac arrhythmias. Recent data suggest that cardiac glycosides may also be useful in the treatment of cancer. These compounds typically inhibit cancer cell proliferation at nanomolar concentrations, and recent high-throughput screenings of drug libraries have therefore identified cardiac glycosides as potent inhibitors of cancer cell growth. Cardiac glycosides can also block tumor growth in rodent models, which further supports the idea that they have potential for cancer therapy. Evidence also suggests, however, that cardiac glycosides may not inhibit cancer cell proliferation selectively and the potent inhibition of tumor growth induced by cardiac glycosides in mice xenografted with human cancer cells is probably an experimental artifact caused by their ability to selectively kill human cells versus rodent cells. This paper reviews such evidence and discusses experimental approaches that could be used to reveal the cancer therapeutic potential of cardiac glycosides in preclinical studies.

Indexed as

AnimalsAntineoplastic AgentsCardiac GlycosidesDrug Evaluation, PreclinicalHumansNeoplasmsAntineoplastic AgentsCardiac Glycosides

Identifiers

PMID24895612
PMCPMC4033509
OpenAlexW2099686861

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.