Evidence map›Paper›PMID 30262730›Full record

ReviewCancers2018

Ionophores: Potential Use as Anticancer Drugs and Chemosensitizers.

Vivek Kaushik, Juan Sebastian Yakisich, Anil Kumar, Neelam Azad, Anand K V Iyer

Abstract readReview
In one paragraph

Review in Cancers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
–field-weighted citation impact
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

40 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Mechanistic basis for potassium efflux-driven activation of the human NLRP1 inflammasome.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Ionophore Toxicity in Animals: A Review of Clinical and Molecular Aspects.International journal of molecular sciences · 2023
    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

5 authors.

Vivek KaushikDepartment of Pharmaceutical Sciences, School of Pharmacy, Hampton University, Hampton, VA 23668, USA. vivek.kaushik@hamptonu.edu.
Juan Sebastian YakisichDepartment of Pharmaceutical Sciences, School of Pharmacy, Hampton University, Hampton, VA 23668, USA. juan.yakisich@hamptonu.edu.
Anil KumarGreat Plains Health, North Platte, NE 69101, USA. kumara@gphealth.org.
Neelam AzadDepartment of Pharmaceutical Sciences, School of Pharmacy, Hampton University, Hampton, VA 23668, USA. neelam.azad@hamptonu.edu.
Anand K V IyerDepartment of Pharmaceutical Sciences, School of Pharmacy, Hampton University, Hampton, VA 23668, USA. anand.iyer@hamptonu.edu.

Funding

The Hampton University regional Transdisciplinary Collaborative CenterU54MD008621 · NIMHD · HAMPTON UNIVERSITY · PI SAMUEL, RAYMOND E · 2013 to 2017
$13.5M
Impact of Oxidative Stress-Regulated Angiogenesis in Pulmonary FibrosisSC1HL112630 · NHLBI · HAMPTON UNIVERSITY · PI AZAD, NEELAM · 2011 to 2015
$1.3M
Targeting Lipogenic and Angiogenic Mediators in Pulmonary FibrosisSC1GM121287 · NIGMS · HAMPTON UNIVERSITY · PI AZAD, NEELAM · 2018 to 2021
$1.3M
NHLBI NIH HHS SC1 HL112630NIGMS NIH HHS SC1 GM121287NIH HHS 9SC1GM121287-06A1NIH HHS U54MD008621
6 · The paper itself

Abstract

Ion homeostasis is extremely important for the survival of both normal as well as neoplastic cells. The altered ion homeostasis found in cancer cells prompted the investigation of several ionophores as potential anticancer agents. Few ionophores, such as Salinomycin, Nigericin and Obatoclax, have demonstrated potent anticancer activities against cancer stem-like cells that are considered highly resistant to chemotherapy and responsible for tumor relapse. The preclinical success of these compounds in in vitro and in vivo models have not been translated into clinical trials. At present, phase I/II clinical trials demonstrated limited benefit of Obatoclax alone or in combination with other anticancer drugs. However, future development in targeted drug delivery may be useful to improve the efficacy of these compounds. Alternatively, these compounds may be used as leading molecules for the development of less toxic derivatives.

Indexed as

chemosensitizationcombination chemotherapyionophoresnigericinobatoclaxsalinomycinstem cells

Identifiers

PMID30262730
PMCPMC6211070

What OpenQuestion holds

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Registered trials

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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.