Evidence map›Paper›PMID 27377046›Full record

ArticleAngewandte Chemie (International ed. in English)2016

Activation of Platinum(IV) Prodrugs By Motexafin Gadolinium as a Redox Mediator.

Gregory Thiabaud, Rebecca McCall, Guangan He, Jonathan F Arambula, Zahid H Siddik, Jonathan L Sessler

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.4field-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

18 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Chemical science · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Oxaliplatin Pt(IV) prodrugs conjugated to gadolinium-texaphyrin as potential antitumor agents.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Hypoxia-targeted drug delivery.Chemical Society reviews · 2019
    Review
  17. Article
  18. 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

6 authors at 3 institutions in 1 country.

Gregory ThiabaudDepartment of Chemistry and Biochemistry, University of Texas at Austin, 105 E. 24th St. Stop A5300, Austin, TX, 78712-1224, USA.
Rebecca McCallDepartment of Chemistry, Georgia Southern University, Statesboro, GA, 30460, USA.
Guangan HeThe University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Blvd., Unit Number: 1950, Houston, TX, 77030, USA.
Jonathan F ArambulaDepartment of Chemistry, Georgia Southern University, Statesboro, GA, 30460, USA.
Zahid H SiddikThe University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Blvd., Unit Number: 1950, Houston, TX, 77030, USA. zsiddik@mdanderson.org.
Jonathan L SesslerDepartment of Chemistry and Biochemistry, University of Texas at Austin, 105 E. 24th St. Stop A5300, Austin, TX, 78712-1224, USA. sessler@cm.utexas.edu.ORCID 0000-0002-9576-1325
Georgia Southern University · USThe University of Texas at Austin · USThe University of Texas MD Anderson Cancer Center · US

Funding

Biomedical Applications of Expanded Porphyrins: Development of Gold-Texaphyrin ConjugatesR01CA068682 · NCI · UNIVERSITY OF TEXAS AUSTIN · PI Esther Y. Maier, Emily L Que · 1995 to 2026
$7.4M
Targeted Development of Platinum DrugsR01CA160687 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SIDDIK, ZAHID H · 2011 to 2015
$1.6M
NCI NIH HHS R01 CA068682NCI NIH HHS R01 CA160687
6 · The paper itself

Abstract

Water-soluble platinum(IV) prodrugs, which proved kinetically stable to reduction in the presence of physiological concentration of ascorbate, were quickly reduced to their active form, oxaliplatin, when co-incubated with a macrocycle metallotexaphyrin (i.e., Motexafin Gadolinium (MGd)). The reduction of Pt(IV) to Pt(II) promoted by MGd occurs in cell culture as well, leading to an increase in the antiproliferative activity of the Pt(IV) species in question. The mediated effect is proportional to the concentration of MGd and gives rise to an enhancement when the prodrug is relatively hydrophilic. MGd is known to localize/accumulate preferentially in tumor tissues. Thus, the present "activation by reduction" approach may allow for the cancer-selective enhancement in the cytotoxicity of Pt(IV) prodrugs.

Indexed as

Antineoplastic AgentsCell Line, TumorCell ProliferationElectrochemical TechniquesHumansMetalloporphyrinsOxidation-ReductionPlatinumProdrugsAntineoplastic AgentsMetalloporphyrinsmotexafin gadoliniumPlatinumProdrugsantitumor agentsmetallotexaphyrinplatinumprodrugsredox chemistry

Identifiers

PMID27377046
PMCPMC5039070
OpenAlexW2464143334

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.