Evidence map›Paper›PMID 20676117›Full record

ReviewActa pharmacologica Sinica2010

Poly(ADP-ribose) polymerase inhibitors as promising cancer therapeutics.

Jin-xue He, Chun-hao Yang, Ze-hong Miao

Abstract readReview
In one paragraph

Review in Acta pharmacologica Sinica, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

  1. LncRNAInternational journal of molecular sciences · 2023
    Article
  2. Article
  3. Article
  4. Article
  5. Identification of probe-quality degraders for Poly(ADP-ribose) polymerase-1 (PARP-1).Journal of enzyme inhibition and medicinal chemistry · 2020
    Article
  6. Article
  7. Novel mutations inAmerican journal of cancer research · 2020
    Article
  8. Review
  9. Biological Potential and Mechanism of Prodigiosin fromInternational journal of molecular sciences · 2018
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. DNA repair: from genome maintenance to biomarker and therapeutic target.Clinical cancer research : an official journal of the American Association for Cancer Research · 2011
    Review
  18. Article
  19. PARP and cancer--if it's broke, don't fix it.The New England journal of medicine · 2011
    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

3 authors.

Jin-xue HeShanghai Institute of Materia Medica, Chinese Academy of Sciences, Zhang Jiang Hi-Tech Park, China.
Chun-hao Yang
Ze-hong Miao

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The year of 2005 was a watershed in the history of poly(ADP-ribose) polymerase (PARP) inhibitors due to the important findings of selective killing in BRCA-deficient cancers by PARP inhibition. The findings made PARP inhibition one of the most promising new therapeutic approaches to cancers, especially to those with specific defects. With AZD2281 and BSI-201 entering phase III clinical trials, the final application of PARP inhibitors in clinic would come true soon. This current paper will review the major advances in targeting PARP for cancer therapy and discuss the existing questions, the answers to which may influence the future of PARP inhibitors as cancer therapeutics.

Indexed as

Poly(ADP-ribose) Polymerase InhibitorsAnimalsAntineoplastic AgentsClinical Trials as TopicEnzyme InhibitorsHumansNeoplasmsPoly(ADP-ribose) PolymerasesAntineoplastic AgentsEnzyme InhibitorsPoly(ADP-ribose) Polymerase InhibitorsPoly(ADP-ribose) Polymerases

Identifiers

PMID20676117
PMCPMC4002295

What OpenQuestion holds

Textmetadata
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.