Evidence map›Paper›PMID 24272524›Full record

ArticleCell biology and toxicology2013

Analysis of the cytotoxic effects of ruthenium-ketoconazole and ruthenium-clotrimazole complexes on cancer cells.

Elisa Robles-Escajeda, Alberto Martínez, Armando Varela-Ramirez, Roberto A Sánchez-Delgado, Renato J Aguilera

Open access · greenAbstract read
In one paragraph

Article in Cell biology and toxicology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
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  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Ruthenium (II) complex cis-[RuScientific reports · 2020
    Article
  11. Article
  12. Article
  13. Anticancer activity of novel amino acid derivative of palladium complex with phendione ligand against of human colon cancer cell line.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2017
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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 at 3 institutions in 1 country.

Elisa Robles-EscajedaBorder Biomedical Research Center and Department of Biological Sciences, The University of Texas at El Paso, El Paso, TX, 79968, USA.
Alberto Martínez
Armando Varela-Ramirez
Roberto A Sánchez-Delgado
Renato J Aguilera
The University of Texas at El Paso · USBrooklyn College · USCity University of New York · US

Funding

TOXICOLOGY PROJECTG12RR008124 · NCRR · UNIVERSITY OF TEXAS EL PASO · PI WALSH, ELIZABETH J · 1992 to 2011
$20.8M
TCCG12MD007592 · NIMHD · UNIVERSITY OF TEXAS EL PASO · PI KIRKEN, ROBERT A. · 2012 to 2018
$19.4M
RISE Scholars Program at UTEPR25GM069621 · NIGMS · UNIVERSITY OF TEXAS EL PASO · PI AGUILERA, RENATO J · 2004 to 2021
$11.2M
Ruthenium-based antimalarial agentsSC1GM089558 · NIGMS · BROOKLYN COLLEGE · PI SANCHEZ-DELGADO, ROBERTO A · 2010 to 2013
$1.2M
Characterization of novel compounds with anti-lymphoma activitySC3GM103713 · NIGMS · UNIVERSITY OF TEXAS EL PASO · PI AGUILERA, RENATO J · 2013 to 2016
$453k
NCRR NIH HHS G12 RR008124NIGMS NIH HHS R25 GM069621NIGMS NIH HHS SC1 GM089558NIGMS NIH HHS SC3 GM103713NIMHD NIH HHS 8G12MD007592NIMHD NIH HHS G12 MD007592
6 · The paper itself

Abstract

Ruthenium-based compounds have intriguing anti-cancer properties, and some of these novel compounds are currently in clinical trials. To continue the development of new metal-based drug combinations, we coupled ruthenium (Ru) with the azole compounds ketoconazole (KTZ) and clotrimazole (CTZ), which are well-known antifungal agents that also display anticancer properties. We report the activity of a series of 12 Ru-KTZ and Ru-CTZ compounds against three prostate tumor cell lines with different androgen sensitivity, as well as cervical cancer and lymphoblastic lymphoma cell lines. In addition, human cell lines were used to evaluate the toxicity against non-transformed cells and to establish selectivity indexes. Our results indicate that the combination of ruthenium and KTZ/CTZ in a single molecule results in complexes that are more cytotoxic than the individual components alone, displaying in some cases low micromolar CC50 values and high selectivity indexes. Additionally, all compounds are more cytotoxic against prostate cell lines with lower cytotoxicity against non-transformed epidermal cell lines. Some of the compounds were found to primarily induce cell death via apoptosis yet weakly interact with DNA. Our studies also demonstrate that the cytotoxicity induced by our Ru-based compounds is not directly related to their ability to interact with DNA.

Indexed as

ApoptosisCell Line, TumorClotrimazoleDNA, NeoplasmHumansKetoconazoleMaleProstatic NeoplasmsRutheniumClotrimazoleDNA, NeoplasmKetoconazoleRuthenium

Identifiers

PMID24272524
PMCPMC4207122
OpenAlexW2088878860

What OpenQuestion holds

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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.