Evidence map›Paper›PMID 19110069›Full record

ReviewThe international journal of biochemistry & cell biology2009

In vitro non-homologous DNA end joining assays--the 20th anniversary.

Elzbieta Pastwa, Richard I Somiari, Mariusz Malinowski, Stella B Somiari, Thomas A Winters

Open access · greenAbstract readReview
In one paragraph

Review in The international journal of biochemistry & cell biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

15 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Establishment of a Transformation CoupledFrontiers in oncology · 2020
    Article
  6. Article
  7. Ovarian Cancers Harbor Defects in Nonhomologous End Joining Resulting in Resistance to Rucaparib.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

5 authors at 3 institutions in 2 countries.

Elzbieta PastwaDepartment of Molecular Genetics, Medical University of Lodz, Mazowiecka 6/8, 92-215 Lodz, Poland. epastwa@csk.umed.lodz.pl
Richard I Somiari
Mariusz Malinowski
Stella B Somiari
Thomas A Winters
Medical University of Lodz · PLNational Institutes of Health · USWindber Research Institute · US

Funding

Gene-targetted RadiotherapyZ01CL060001 · CLC · CLINICAL CENTER · PI NEUMANN, RONALD · 1997 to 2008
$1.9M
Investigating DNA repair vulnerabilities in oncometabolite producing cancersF31CA260794 · NCI · YALE UNIVERSITY · PI NORONHA, KATELYN · 2021 to 2023
$122k
Intramural NIH HHS Z01 CL060001Intramural NIH HHS Z99 CL999999NCI NIH HHS F31 CA260794
6 · The paper itself

Abstract

DNA double-strand breaks (DSBs) are the most serious forms of DNA damage in cells. Unrepaired or misrepaired DSBs account for some of the genetic instabilities that lead to mutations or cell death, and consequently, to cancer predisposition. In human cells non-homologous DNA end joining (NHEJ) is the main repair mechanism of these breaks. Systems for DNA end joining study have been developing during the last 20 years. New assays have some advantages over earlier in vitro DSBs repair assays because they are less time-consuming, allow the use of clinical material and examination of the joining DNA ends produced physiologically in mammalian cells. Proteins involved in NHEJ repair pathway can serve as biomarkers or molecular targets for anticancer drugs. Results of studies on NHEJ in cancer could help to select potent repair inhibitors that may selectively sensitize tumor cells to ionizing radiation (IR) and chemotherapy. Here, we review the principles and practice of in vitro NHEJ assays and provide some insights into the future prospects of this assay in cancer diagnosis and treatment.

Indexed as

DNA Breaks, Double-StrandedDNA RepairAnimalsDNA Repair EnzymesHumansDNA Repair Enzymes

Identifiers

PMID19110069
PMCPMC2901157
OpenAlexW2010822709

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.