Evidence map›Paper›PMID 20694266›Full record

ArticleChemical communications (Cambridge, England)2010

Excursions in polynuclear platinum DNA binding.

John B Mangrum, Nicholas P Farrell

Open access · greenAbstract read
In one paragraph

Article in Chemical communications (Cambridge, England), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 109 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

John B MangrumDepartment of Chemistry, Virginia Commonwealth University, 1001 W. Main Street, Richmond, VA 23284, USA.
Nicholas P Farrell
Virginia Commonwealth University · US

Funding

MECHANISTIC STUDIES ON NEW PLATINUM CLINICAL AGENTSR01CA078754 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FARRELL, NICHOLAS P · 1998 to 2012
$3.6M
NCI NIH HHS R01 CA078754NCI NIH HHS R01CA78754
6 · The paper itself

Abstract

Polynuclear platinum agents are a structurally unique class of anti-cancer drugs, distinct from the cisplatin family. To describe the chemistry and biology of this class, it was necessary to challenge the accepted paradigms for the structure-activity relationships; design new chemotypes and delineate the structures and consequences of their DNA binding modes. This article summarizes the structural changes induced in DNA by both covalent (bond-forming) and non-covalent (ligand recognition) adducts. Solution (Nuclear Magnetic Resonance), solid state (crystallography) and gas-phase (Electrospray Ionization Mass Spectrometry) techniques have all been used to describe the new DNA structures along with molecular biological techniques. The combined approaches allow molecular description of hitherto unobserved adducts such as long-range major-groove interstrand crosslinks; directional isomers on DNA and a third class of ligand-DNA binding, the phosphate clamp. The phosphate recognition is distinct from ''classic'' minor-groove recognition or intercalation.

Indexed as

Antineoplastic AgentsCross-Linking ReagentsDNADNA AdductsIsomerismNuclear Magnetic Resonance, BiomolecularPlatinumSpectrometry, Mass, Electrospray IonizationStructure-Activity RelationshipAntineoplastic AgentsCross-Linking ReagentsDNADNA AdductsPlatinum

Identifiers

PMID20694266
PMCPMC3018806
OpenAlexW1993837819

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.