Evidence map›Paper›PMID 19377506›Full record

ReviewNature reviews. Cancer2009

Targeting DNA topoisomerase II in cancer chemotherapy.

John L Nitiss

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Cancer, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 849 papers.

0numbers the graph read from it
0cells of the map it votes in
849citing papers in PubMed
28.9field-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

849 citing papers in PubMed, 1,753 citations in OpenAlex.

  1. Trial
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  6. A multispecies toolkit ofProceedings of the National Academy of Sciences of the United States of America · 2026
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  9. Review
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  16. Rebinding drives cellular retention of small-molecule drugs with abundant targets.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  18. Article
  19. Review
  20. Article

789 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

1 author at 1 institution in 1 country.

John L NitissMolecular Pharmacology Department, St Jude Children's Research Hospital, Memphis, TN 38105, USA. john.nitiss@stjude.org
St. Jude Children's Research Hospital · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
ANTITOPOISOMERASE DRUG ACTION IN YEASTR01CA052814 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI NITISS, JOHN L · 1990 to 2014
$2.7M
DNA REPAIR AND ANTITOPOISOMERASE DRUG EFFECTSR01CA082313 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI NITISS, JOHN L · 1999 to 2010
$2.3M
NCI NIH HHS CA21765NCI NIH HHS CA82313NCI NIH HHS P30 CA021765NCI NIH HHS R01 CA052814NCI NIH HHS R01 CA082313
6 · The paper itself

Abstract

Recent molecular studies have expanded the biological contexts in which topoisomerase II (TOP2) has crucial functions, including DNA replication, transcription and chromosome segregation. Although the biological functions of TOP2 are important for ensuring genomic integrity, the ability to interfere with TOP2 and generate enzyme-mediated DNA damage is an effective strategy for cancer chemotherapy. The molecular tools that have allowed an understanding of the biological functions of TOP2 are also being applied to understanding the details of drug action. These studies promise refined targeting of TOP2 as an effective anticancer strategy.

Indexed as

Topoisomerase II InhibitorsAnimalsAntineoplastic AgentsCatalysisDNADNA RepairDNA Topoisomerases, Type IIEnzyme InhibitorsHumansAntineoplastic AgentsDNADNA Topoisomerases, Type IIEnzyme InhibitorsTopoisomerase II Inhibitors

Identifiers

PMID19377506
PMCPMC2748742
OpenAlexW2041051519

What OpenQuestion holds

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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.