Evidence map›Paper›PMID 26717259›Full record

ArticleJournal of inorganic biochemistry2016

Novel enantiopure cyclopentadienyl Ti(IV) oximato compounds as potential anticancer agents.

Isabel de la Cueva-Alique, Laura Muñoz-Moreno, Yosra Benabdelouahab, Benelita T Elie, Mohammed Amin El Amrani, Marta E G Mosquera, María Contel, Ana M Bajo, Tomás Cuenca, Eva Royo

Open access · greenAbstract read
In one paragraph

Article in Journal of inorganic biochemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. RacemicRSC advances · 2018
    Article
  3. Article
  4. Specific Interactions of Antitumor Metallocenes with Deoxydinucleoside Monophosphates.Journal of the American Society for Mass Spectrometry · 2017
    Article
  5. 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

10 authors at 3 institutions in 3 countries.

Isabel de la Cueva-AliqueDepartamento de Química Orgánica y Química Inorgánica, Facultad de Biología, Ciencias Ambientales y Química, Universidad de Alcalá, 28871 Alcalá de Henares, Madrid, Spain.
Laura Muñoz-MorenoDepartamento de Biología de Sistemas, Facultad de Biología, Ciencias Ambientales y Química, Universidad de Alcalá, 28871 Alcalá de Henares, Madrid, Spain.
Yosra BenabdelouahabDepartamento de Química Orgánica y Química Inorgánica, Facultad de Biología, Ciencias Ambientales y Química, Universidad de Alcalá, 28871 Alcalá de Henares, Madrid, Spain.
Benelita T ElieDepartment of Chemistry, Brooklyn College, The City University of New York, Brooklyn, New York, NY 11210, USA; Chemistry and Biology PhD Programs, The Graduate Center, The City University of New York, 365 Fifth Avenue, New York, NY, 10016, USA.
Mohammed Amin El AmraniUniversité Abdelmalek Essaadi, Departement de Chemie-Laboratoire de Chimie Organique Appliquée, Mhannech II, B.P. 2121, Tétouan, Morocco.
Marta E G MosqueraDepartamento de Química Orgánica y Química Inorgánica, Facultad de Biología, Ciencias Ambientales y Química, Universidad de Alcalá, 28871 Alcalá de Henares, Madrid, Spain.
María ContelDepartment of Chemistry, Brooklyn College, The City University of New York, Brooklyn, New York, NY 11210, USA; Chemistry and Biology PhD Programs, The Graduate Center, The City University of New York, 365 Fifth Avenue, New York, NY, 10016, USA.
Ana M BajoDepartamento de Biología de Sistemas, Facultad de Biología, Ciencias Ambientales y Química, Universidad de Alcalá, 28871 Alcalá de Henares, Madrid, Spain.
Tomás CuencaDepartamento de Química Orgánica y Química Inorgánica, Facultad de Biología, Ciencias Ambientales y Química, Universidad de Alcalá, 28871 Alcalá de Henares, Madrid, Spain.
Eva RoyoDepartamento de Química Orgánica y Química Inorgánica, Facultad de Biología, Ciencias Ambientales y Química, Universidad de Alcalá, 28871 Alcalá de Henares, Madrid, Spain. Electronic address: eva.royo@uah.es.
Universidad de Alcalá · ESThe Graduate Center, CUNY · USAbdelmalek Essaâdi University · MA

Funding

Titanium-gold-based chemotherapeutics for prostate and kidney cancerSC1CA182844 · NCI · BROOKLYN COLLEGE · PI CONTEL, MARIA · 2013 to 2016
$1.4M
NCI NIH HHS SC1 CA182844
6 · The paper itself

Abstract

The synthesis and characterization of new enantiopure cyclopentadienyl titanium oximato compounds (S,R)-[(η(5)-C5H5)Ti{к(2)NO,(R)NH·HCl}Cl2] (R=Ph (phenyl) 1a·HCl, Bn (benzyl) 1b·HCl, 2-pic (2-picolyl) 1c·HCl), (S,R)-[(η(5)-C5H5)TiCl2{к(2)NO,(Ph)NH}] (1a) and (S,R)-[(η(5)-C5H5)2TiCl{к(2)NO,(R)NH}] (R=Ph 2a, Bn 2b, 2-pic 2c), along with studies on their behavior in D2O at different pD values are reported. The structure of previously described ammonium-oxime (2S,5R)-{NOH,(Bn)NH·HCl} (b·HCl) and novel titanium derivative 1a have been determined by single crystal X-ray crystallography. The effect of the compounds on cytotoxicity, cell adhesion and migration of the androgen-independent prostate cancer PC-3 cells has been assessed. Compounds 2b and 2c are more cytotoxic than additive doses of titanocene dichloride and free oxime proligand, probing the synergistic effect of these novel compounds. The cytotoxicity of 2b and 2c has been further evaluated against human renal Caki-1, colon DLD-1 and triple negative breast MDA-MB-231 cancer cell lines. The activity found for 2c on PC-3 and Caki-1 is higher than that of highly active Titanocene Y (bis-[(p-methoxybenzyl)cyclopentadienyl]titanium(IV) dichloride), while showing selectivity against renal cancer when compared to a non-tumorigenic human renal (HEK-293T) cell line. Compounds 2b and especially 2c are apoptotic in Caki-1 cancer cell lines. Cell adhesion and wound-healing assays confirmed that derivatives 1c·HCl, 2b and 2c affect the adhesion and migration patterns of the PC-3 cell line. Interactions of the novel compounds with plasmid (pBR322) DNA have also been studied, showing that the oximato Ti(IV) derivatives have a weak or no interaction with DNA at physiological pH.

Indexed as

Antineoplastic AgentsCell Line, TumorCrystallography, X-RayHumansMagnetic Resonance SpectroscopyMaleSpectroscopy, Fourier Transform InfraredStereoisomerismTitaniumAntineoplastic AgentsTitaniumCell adhesionCell migrationChiralityCyclopentadienyl titanium compoundsDNAPC-3 and Caki-1 cell lines

Identifiers

PMID26717259
PMCPMC4882921
OpenAlexW2196283803

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.