Evidence map›Paper›PMID 20534341›Full record

ReviewChemistry & biology2010

DNA topoisomerases and their poisoning by anticancer and antibacterial drugs.

Yves Pommier, Elisabetta Leo, HongLiang Zhang, Christophe Marchand

Open access · greenAbstract readReview
In one paragraph

Review in Chemistry & biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 834 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
834citing papers in PubMed, 1 pooled it
33.0field-weighted citation impact, top 1% 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

834 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,810 citations in OpenAlex.

  1. Pooled it
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774 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Yves PommierLaboratory of Molecular Pharmacology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-4255, USA. pommier@nih.gov
Elisabetta Leo
HongLiang Zhang
Christophe Marchand
National Institutes of Health · US

Funding

DNA Topoisomerases as Target of Action of Anticancer DrugsZIABC006161 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI POMMIER, YVES · 2009 to 2025
$16.8M
PHARMACOLOGY OF THE HIV VIRAL DNA AND RETROVIRAL INTEGRASESZ01BC007333 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI POMMIER, YVES · 1996 to 2008
$1.0M
Intramural NIH HHS Z01 BC007333
6 · The paper itself

Abstract

DNA topoisomerases are the targets of important anticancer and antibacterial drugs. Camptothecins and novel noncamptothecins in clinical development (indenoisoquinolines and ARC-111) target eukaryotic type IB topoisomerases (Top1), whereas human type IIA topoisomerases (Top2alpha and Top2beta) are the targets of the widely used anticancer agents etoposide, anthracyclines (doxorubicin, daunorubicin), and mitoxantrone. Bacterial type II topoisomerases (gyrase and Topo IV) are the targets of quinolones and aminocoumarin antibiotics. This review focuses on the molecular and biochemical characteristics of topoisomerases and their inhibitors. We also discuss the common mechanism of action of topoisomerase poisons by interfacial inhibition and trapping of topoisomerase cleavage complexes.

Indexed as

Topoisomerase InhibitorsAnti-Bacterial AgentsAntineoplastic AgentsCamptothecinDNA TopoisomerasesDoxorubicinEnzyme InhibitorsEtoposideHumansMitoxantroneQuinolonesAnti-Bacterial AgentsAntineoplastic AgentsCamptothecinDNA TopoisomerasesDoxorubicinEnzyme InhibitorsEtoposideMitoxantroneQuinolonesTopoisomerase Inhibitors

Identifiers

PMID20534341
PMCPMC7316379
OpenAlexW2068577449

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.